S. Ikeda

发表

Up-regulation of mitogen activated protein kinases in mdx skeletal muscle following chronic treadmill exercise.

A. Nakamura, Kunihiro Yoshida, H. Ueda, 2005, Biochimica et biophysica acta.

Autosomal-recessive complicated spastic paraplegia with a novel lysosomal trafficking regulator gene mutation

S. Tsuji, Kunihiro Yoshida, S. Ikeda, 2014, Journal of Neurology, Neurosurgery & Psychiatry.

On the errors in assessment of severity of involuntary movements using surface EMG.

M. Shindo, H. Morita, T. Hashimoto, 2005, Journal of electromyography and kinesiology : official journal of the International Society of Electrophysiological Kinesiology.

Unexpectedly high incidence of visceral AA-amyloidosis in slaughtered cattle in Japan

T. Tokuda, F. Kametani, S. Ikeda, 2005, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Slaughtered aged cattle might be one dietary source exhibiting amyloid enhancing factor activity

S. Ikeda, Xiaoying Fu, K. Higuchi, 2009, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Morphology and distribution of plaque and related deposits in the brains of Alzheimer's disease and control cases. An immunohistochemical study using amyloid beta-protein antibody.

G. Glenner, D. Allsop, S. Ikeda, 1989, Laboratory investigation; a journal of technical methods and pathology.

Event based and time based prospective memory in Parkinson’s disease

T. Hashimoto, T. Maruyama, S. Ikeda, 2003, Journal of neurology, neurosurgery, and psychiatry.

Phenotypic analysis of plasma cells in bone marrow using flow cytometry in AL amyloidosis

S. Ikeda, Y. Hoshii, Y. Shimojima, 2003, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Type I (transthyretin Met30) familial amyloid polyneuropathy in Japan: early- vs late-onset form.

G. Sobue, S. Ikeda, M. Nakazato, 2002, Archives of neurology.

Ten years of experience with liver transplantation for familial amyloid polyneuropathy in Japan: outcomes of living donor liver transplantations.

S. Ikeda, Y. Ando, S. Miyagawa, 2005, Internal medicine.

Ten-year follow-up of peripheral nerve function in patients with familial amyloid polyneuropathy after liver transplantation

H. Morita, S. Ikeda, Y. Takei, 2008, Journal of Neurology.

Marked regression of abdominal fat amyloid in patients with familial amyloid polyneuropathy during long‐term follow‐up after liver transplantation

F. Kametani, S. Ikeda, M. Yazaki, 2008, Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society.

Diagnostic value of abdominal wall fat pad biopsy in senile systemic amyloidosis

J. Koyama, S. Ikeda, K. Tojo, 2011, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Amyloid fibrils containing fragmented ATTR may be the standard fibril composition in ATTR amyloidosis

C. Rapezzi, J. Liepnieks, M. Benson, 2013, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Guideline of transthyretin-related hereditary amyloidosis for clinicians

Yukio Ando, Teresa Coelho, Fabrizio Salvi, 2013, Orphanet Journal of Rare Diseases.

Liver Transplantation for Hereditary Transthyretin Amyloidosis: After 20 Years Still the Best Therapeutic Alternative?

N. Heaton, D. Samuel, G. Otto, 2015, Transplantation.

Amyloid fibril proteins and amyloidosis: chemical identification and clinical classification International Society of Amyloidosis 2016 Nomenclature Guidelines

Giampaolo Merlini, Shu-Ichi Ikeda, Per Westermark, 2016, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Echocardiographic assessment of the cardiac amyloidoses.

J. Koyama, S. Ikeda, Uichi Ikeda, 2015, Circulation journal : official journal of the Japanese Circulation Society.

High-dose melphalan followed by autologous stem cell support in primary systemic AL amyloidosis with multiple organ involvement.

J. Koyama, S. Ikeda, K. Koike, 2005, Internal medicine.

Cardiac amyloidosis: heterogenous pathogenic backgrounds.

S. Ikeda, 2004, Internal medicine.

Postpartum Anti-N-methyl-D-aspartate Receptor Encephalitis: A Case Report and Literature Review

N. Tachibana, S. Ikeda, T. Doden, 2017, Internal medicine.

A case of Mikulicz's disease complicated by malignant lymphoma: a postmortem histopathological finding.

E. Hara, S. Ikeda, S. Kawa, 2012, Internal medicine.

A novel frameshift mutation in the McLeod syndrome gene in a Japanese family

A. Nakamura, Kunihiro Yoshida, S. Ikeda, 1999, Journal of the Neurological Sciences.

Sporadic hereditary diffuse leukoencephalopathy with axonal spheroids showing numerous lesions with restricted diffusivity caused by a novel splice site mutation in the CSF1R gene

Satoshi O. Suzuki, T. Iwaki, J. Kira, 2013 .

Nomenclature 2014: Amyloid fibril proteins and clinical classification of the amyloidosis

M. Benson, M. Saraiva, S. Ikeda, 2014, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Amyloid fibril protein nomenclature: 2012 recommendations from the Nomenclature Committee of the International Society of Amyloidosis

M. Benson, M. Saraiva, S. Ikeda, 2012, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Clinical features of non‐hypertensive lobar intracerebral hemorrhage related to cerebral amyloid angiopathy

M. Yoshita, S. Ikeda, A. Tamaoka, 2010, European journal of neurology.

Cortical petechial hemorrhage, subarachnoid hemorrhage and corticosteroid-responsive leukoencephalopathy in a patient with cerebral amyloid angiopathy

S. Ikeda, K. Tojo, T. Gono, 2008, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Evidence of amyloid beta-protein immunoreactive early plaque lesions in Down's syndrome brains.

G. Glenner, N. Yanagisawa, D. Allsop, 1989, Laboratory investigation; a journal of technical methods and pathology.

Mechanism for increased hepatic glycerol synthesis in the citrin/mitochondrial glycerol-3-phosphate dehydrogenase double-knockout mouse: Urine glycerol and glycerol 3-phosphate as potential diagnostic markers of human citrin deficiency.

T. Saheki, K. Yamamura, T. Kadowaki, 2015, Biochimica et biophysica acta.

The characteristics of food intake in patients with type II citrullinemia.

T. Saheki, Y. Nakaya, S. Ikeda, 2011, Journal of nutritional science and vitaminology.

Conventional diet therapy for hyperammonemia is risky in the treatment of hepatic encephalopathy associated with citrin deficiency.

T. Saheki, S. Ikeda, Keiko Kobayashi, 2010, Internal medicine.

Type II (adult onset) citrullinaemia: clinical pictures and the therapeutic effect of liver transplantation

S. Kawasaki, T. Saheki, S. Ikeda, 2001, Journal of neurology, neurosurgery, and psychiatry.

Hepatocellular carcinoma in a case of adult-onset type II citrullinemia.

S. Kawasaki, T. Saheki, S. Ikeda, 2003, Internal medicine.

Chronic pancreatitis associated with adult-onset type II citrullinemia: clinical and pathologic findings.

T. Saheki, S. Ikeda, Keiko Kobayashi, 2004, Annals of internal medicine.

Risk of worsened encephalopathy after intravenous glycerol therapy in patients with adult-onset type II citrullinemia (CTLN2).

T. Saheki, S. Ikeda, Keiko Kobayashi, 2005, Internal medicine.

Metabolic derangements in deficiency of citrin, a liver-type mitochondrial aspartate-glutamate carrier.

T. Saheki, S. Ikeda, Keiko Kobayashi, 2005, Hepatology research : the official journal of the Japan Society of Hepatology.

Steatogenesis in adult-onset type II citrullinemia is associated with down-regulation of PPARα.

F. Gonzalez, S. Ikeda, T. Aoyama, 2015, Biochimica et biophysica acta.

A −16C>T substitution in the 5′ UTR of the puratrophin-1 gene is prevalent in autosomal dominant cerebellar ataxia in Nagano

Y. Fukushima, N. Matsumoto, Kunihiro Yoshida, 2006, Journal of Human Genetics.

Prevalence and clinical features of cough variant asthma in a general internal medicine outpatient clinic in Japan

S. Ikeda, K. Fujimoto, H. Arioka, 2005, Respirology.

Pathogenesis of and therapeutic strategies to ameliorate the transthyretin amyloidoses.

J. Kelly, S. Ikeda, Y. Sekijima, 2008, Current pharmaceutical design.

A novel splicing mutation in the ceruloplasmin gene responsible for hereditary ceruloplasmin deficiency with hemosiderosis

A. Nakamura, Kunihiro Yoshida, S. Ikeda, 1998, Journal of the Neurological Sciences.

Brain Biopsy Is More Reliable than the DNA test for JC Virus in Cerebrospinal Fluid for the Diagnosis of Progressive Multifocal Leukoencephalopathy

M. Saijo, S. Ikeda, Kenta Takahashi, 2017, Internal medicine.

Genotype-phenotype correlation in Japanese patients with familial Mediterranean fever: differences in genotype and clinical features between Japanese and Mediterranean populations

A. Nakamura, S. Ikeda, M. Yazaki, 2014, Arthritis Research & Therapy.

Periodic peritonitis due to familial Mediterranean fever in a patient with systemic lupus erythematosus.

S. Ikeda, M. Yazaki, Y. Shimojima, 2010, Internal medicine.

Clinical and Genetic Features of Familial Mediterranean Fever in Japan

A. Nakamura, S. Ikeda, M. Yazaki, 2009, The Journal of Rheumatology.

Safety and efficacy of long-term diflunisal administration in hereditary transthyretin (ATTR) amyloidosis

H. Morita, J. Koyama, S. Ikeda, 2015, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Schwann cell and endothelial cell damage in transthyretin familial amyloid polyneuropathy

G. Sobue, S. Ikeda, Y. Ando, 2016, Neurology.

Usefulness of [123I]metaiodobenzylguanidine ([123I]MIBG) myocardial scintigraphy in differentiating between Alzheimer's disease and dementia with Lewy bodies.

A. Nakamura, T. Tokuda, S. Ohara, 2003, Internal medicine.

Temporary Auxiliary Partial Orthotopic Liver Transplantation Using a Small Graft for Familial Amyloid Polyneuropathy

S. Ikeda, S. Miyagawa, T. Ikegami, 2012, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

Intractable Cutaneous Nontuberculous Mycobacteriosis (Mycobacterium abscessus) during Treatment for Systemic Lupus Erythematosus

S. Ikeda, A. Ushiki, Y. Shimojima, 2017, Internal medicine.

Pneumatosis cystoides intestinalis in neuropsychiatric systemic lupus erythematosus with diabetes mellitus: case report and literature review

S. Ikeda, K. Tojo, Y. Shimojima, 2011 .

Pneumatosis cystoides intestinalis in neuropsychiatric systemic lupus erythematosus with diabetes mellitus: case report and literature review

S. Ikeda, K. Tojo, Y. Shimojima, 2011, Modern rheumatology.

Acute respiratory distress syndrome due to systemic lupus erythematosus with hemophagocytic syndrome: an autopsy report

S. Ikeda, M. Matsuda, T. Gono, 2005, Clinical Rheumatology.

Hemolysis, elevated liver enzymes and low platelet (HELLP) syndrome associated with systemic lupus erythematosus.

T. Hashimoto, S. Ikeda, M. Matsuda, 2003, Internal medicine.

Successful treatment of fulminant pulmonary hemorrhage associated with systemic lupus erythematosus

T. Hashimoto, S. Ikeda, M. Matsuda, 2004, Clinical Rheumatology.

Delayed domino liver transplantation: use of the remnant liver of a recipient of a temporary auxiliary orthotopic liver transplant as a liver graft for another patient.

S. Kawasaki, S. Ikeda, S. Miyagawa, 2004, Transplantation.

Polyarteritis nodosa with central nervous system involvement mimicking relapsing–remitting multiple sclerosis

S. Ikeda, M. Matsuda, A. Matsushima, 2012, Modern rheumatology.

Interstitial lung disease associated with amyopathic dermatomyositis: review of 18 cases.

S. Ikeda, M. Hanaoka, Y. Shimojima, 2007, Respiratory medicine.

Takayasu's arteritis in a patient with Crohn's disease: an unexpected association during infliximab therapy.

S. Ikeda, Y. Shimojima, M. Matsuda, 2010, Internal medicine.

Coexistence of IgA nephropathy and undifferentiated spondyloarthropathy in a female patient

S. Ikeda, M. Matsuda, H. Miyagawa, 2006, Clinical Rheumatology.

Slowly progressing lower motor neuron disease caused by a novel duplication mutation in exon 1 of the SOD1 gene

A. Nakamura, S. Ikeda, A. Hineno, 2014, Neurobiology of Aging.

Pathological, biochemical, and biophysical characteristics of the transthyretin variant Y114H (p.Y134H) explain its very mild clinical phenotype

K. Nilsson, F. Kametani, S. Ikeda, 2015, Journal of the peripheral nervous system : JPNS.

Steady turnover of amyloid fibril proteins in gastric mucosa after liver transplantation in familial amyloid polyneuropathy

F. Kametani, S. Ikeda, M. Yazaki, 2013, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Wild-type transthyretin significantly contributes to the formation of amyloid fibrils in familial amyloid polyneuropathy patients with amyloidogenic transthyretin Val30Met.

F. Kametani, S. Ikeda, M. Yazaki, 2011, Human pathology.

Biochemical analysis of deposited amyloid fibrils—Analysis of amyloid protein extracted from small biopsy samples

F. Kametani, S. Ikeda, M. Yazaki, 2010 .

Evaluation of Variant Transthyretins for Diagnosis and Pathogenesis of Familial Amyloidotic Polyneuropathy

H. Jono, S. Ikeda, Masaaki Nakamura, 2009 .

The significance of carpal tunnel syndrome in transthyretin Val30Met familial amyloid polyneuropathy

G. Sobue, S. Ikeda, Y. Ando, 2009, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

SELDI-TOF mass spectrometry evaluation of variant transthyretins for diagnosis and pathogenesis of familial amyloidotic polyneuropathy.

H. Jono, S. Ikeda, M. Mizuguchi, 2009, Clinical chemistry.

Non‐senile wild‐type transthyretin systemic amyloidosis presenting as bilateral carpal tunnel syndrome

S. Ikeda, M. Yazaki, Y. Hoshii, 2008, Journal of the peripheral nervous system : JPNS.

Is familial amyloid polyneuropathy rare?

S. Ikeda, 2007, Neurology.

Biochemical characteristics of variant transthyretins causing hereditary leptomeningeal amyloidosis

T. Tokuda, M. Benson, Y. Shimizu, 2005, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Clinical Picture and Outcome of Transthyretin-Related Familial Amyloid Polyneuropathy (FAP) in Japanese Patients

S. Ikeda, 2002, Clinical chemistry and laboratory medicine.

Hemophagocytic syndrome associated with rheumatoid arthritis : A case report and review of the literature

S. Ikeda, M. Matsuda, T. Gono, 2008 .

Hemophagocytic syndrome associated with rheumatoid arthritis.

S. Ikeda, M. Matsuda, T. Gono, 2007, Internal medicine.

Severe protein losing enteropathy with intractable diarrhea due to systemic AA amyloidosis, successfully treated with corticosteroid and octreotide

A. Nakamura, T. Tokuda, S. Ikeda, 2005, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Malignant lymphoma associated with rheumatoid arthritis, developing shortly after initiation of oral methotrexate.

T. Tokuda, S. Ikeda, Y. Shimojima, 2004, Internal medicine.

Spontaneous pneumoperitoneum: an unusual complication of systemic reactive AA amyloidosis secondary to rheumatoid arthritis

S. Ikeda, M. Matsuda, Tomomi Okano, 2003, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Rheumatoid meningitis: an autopsy report and review of the literature

T. Hashimoto, S. Ikeda, M. Matsuda, 2003, Clinical Rheumatology.

Phenol Congo red staining enhances the diagnostic value of abdominal fat aspiration biopsy in reactive AA amyloidosis secondary to rheumatoid arthritis.

S. Ikeda, M. Matsuda, W. Ishii, 2003, Internal medicine.

Long-term follow-up of systemic reactive AA amyloidosis secondary to rheumatoid arthritis: successful treatment with intermediate-dose corticosteroid.

H. Morita, S. Ikeda, M. Matsuda, 2002, Internal medicine.

Cerebrovascular amyloid in scrapie-affected sheep reacts with antibodies to prion protein

G. Glenner, D. Allsop, S. Ikeda, 1988, Neuroscience Letters.

Regional features of autosomal-dominant cerebellar ataxia in Nagano: clinical and molecular genetic analysis of 86 families

Y. Fukushima, T. Hashimoto, S. Ohara, 2004, Journal of Human Genetics.

Gerstmann-Sträussler-Scheinker disease showing β-protein type cerebellar and cerebral amyloid angiopathy

G. Glenner, N. Yanagisawa, D. Allsop, 2004, Acta Neuropathologica.

Histopathological regression of systemic AA amyloidosis after surgical treatment of a localized Castleman's disease

S. Ikeda, Y. Hoshii, Y. Shimojima, 2006, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Partial liver transplantation from living donors in familial amyloid polyneuropathy

S. Kawasaki, M. Makuuchi, N. Yanagisawa, 1997 .

Abdominal fat aspiration biopsy and genotyping of serum amyloid A contribute to early diagnosis of reactive AA amyloidosis secondary to rheumatoid arthritis.

A. Nakamura, S. Ikeda, M. Matsuda, 2003, Internal medicine.

Mixed connective tissue disease with interstitial pneumonia in HTLV-1 carrier: case report and review of the literature

S. Ikeda, Y. Shimojima, M. Matsuda, 2004, Clinical Rheumatology.

Intravenous immunoglobulin (IVIg) with methylprednisolone pulse therapy for motor impairment of neuralgic amyotrophy: clinical observations in 10 cases.

H. Morita, S. Kusunoki, S. Ikeda, 2012, Internal medicine.

Secretory cleavage site of Alzheimer amyloid precursor protein is heterogeneous in Down's syndrome brain

T. Tokuda, S. Ikeda, Kikuko Tanaka, 1994, FEBS letters.

Clinical manifestations at diagnosis in Japanese patients with systemic AL amyloidosis: a retrospective study of 202 cases with a special attention to uncommon symptoms.

S. Ikeda, M. Matsuda, N. Katoh, 2014, Internal medicine.

Long-term follow-up of plasma cells in bone marrow and serum free light chains in primary systemic AL amyloidosis.

S. Ikeda, K. Koike, Y. Nakazawa, 2008, Internal medicine.

Therapeutic outcome of cyclic VAD (vincristine, doxorubicin and dexamethasone) therapy in primary systemic AL amyloidosis patients.

J. Koyama, S. Ikeda, Takuhiro Yoshida, 2008, Internal medicine.

Systemic AL amyloidosis mimicking rheumatoid arthritis.

S. Ikeda, M. Matsuda, W. Ishii, 2008, Internal medicine.

Correlation between serum levels of free light chain and phenotype of plasma cells in bone marrow in primary AL amyloidosis

S. Ikeda, Y. Hoshii, Y. Shimojima, 2005, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Serum levels of free light chain before and after chemotherapy in primary systemic AL amyloidosis.

S. Ikeda, K. Koike, Y. Shimojima, 2005, Internal medicine.

A Japanese patient with familial Mediterranean fever associated with compound heterozygosity for pyrin variant E148Q/M694I.

A. Nakamura, T. Tokuda, S. Ikeda, 2005, Internal medicine.

Hypertrophic pachymeningitis is a characteristic manifestation of granulomatosis with polyangiitis: A retrospective study of anti‐neutrophil cytoplasmic antibody‐associated vasculitis

S. Ikeda, M. Yazaki, Y. Shimojima, 2017, International journal of rheumatic diseases.

Doppler echocardiographic study . amyloid polyneuropathy : a pulsed filling in patients with familial Impaired left ventricular diastolic

S. Ikeda, M. Hongo, O. Kinoshita, 2005 .

Impaired left ventricular diastolic filling in patients with familial amyloid polyneuropathy: a pulsed Doppler echocardiographic study.

S. Ikeda, M. Hongo, O. Kinoshita, 1989, British heart journal.

Impaired left ventricular diastolic filling inpatients withfamilial amyloid polyneuropathy: apulsed Doppler echocardiographic study

S. Ikeda, M. Hongo, O. Kinoshita, 1989 .

Early identification of amyloid heart disease by technetium-99m-pyrophosphate scintigraphy: a study with familial amyloid polyneuropathy.

S. Ikeda, M. Hongo, H. Yamada, 1987, American heart journal.

Principal component analysis for ataxic gait using a triaxial accelerometer

Hirokazu Genno, Kunihiro Yoshida, Shu-ichi Ikeda, 2017, Journal of NeuroEngineering and Rehabilitation.

A Japanese case of familial Mediterranean fever with homozygosity for the pyrin E148Q mutation.

A. Nakamura, S. Ikeda, Toshiro Suzuki, 2005, Internal medicine.

Imbalanced expression of dysfunctional regulatory T cells and T-helper cells relates to immunopathogenesis in polyarteritis nodosa

S. Ikeda, Y. Shimojima, W. Ishii, 2017, Modern rheumatology.

[A Case of Microscopic Polyangiitis with Hypertrophic Pachymeningitis and Diabetes Insipidus].

S. Ikeda, Takuhiro Yoshida, W. Ishii, 2015, Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine.

Serum amyloid A as a potent therapeutic marker in a refractory patient with polymyalgia rheumatica.

S. Ikeda, Y. Shimojima, M. Matsuda, 2005, Internal medicine.

Successful treatment with rituximab in a patient with stiff-person syndrome complicated by dysthyroid ophthalmopathy.

H. Morita, S. Ikeda, M. Matsuda, 2010, Internal medicine.

Progressive supranuclear palsy with asymmetric tau pathology presenting with unilateral limb dystonia

T. Tokuda, S. Ohara, S. Ikeda, 2002, Acta Neuropathologica.

Hereditary ceruloplasmin deficiency with hemosiderosis: A clinicopathological study of a japanese family

H. Morita, N. Yanagisawa, Kunihiro Yoshida, 1995, Annals of neurology.

Plasma levels of amyloid beta proteins Abeta1-40 and Abeta1-42(43) are elevated in Down's syndrome.

T. Tokuda, N. Yanagisawa, S. Ikeda, 1997, Annals of neurology.

A novel nonsense mutation in a Japanese family with ataxia with oculomotor apraxia type 2 (AOA2)

E. Kitamura, Kunihiro Yoshida, S. Ikeda, 2009, Journal of Human Genetics.

Noradrenergic nerve fibers of the rectal mucosa in autonomic disorders: comparison of histochemical study with clinical severity and changes in plasma noradrenaline induced by standing

N. Yanagisawa, S. Ikeda, M. Yazawa, 1991, Journal of the Neurological Sciences.

Spinal form cerebrotendinous xanthomatosis patient with long spinal cord lesion

Takeo Kato, S. Ikeda, Y. Sekijima, 2016, The journal of spinal cord medicine.

Progression of dystrophic features and activation of mitogen‐activated protein kinases and calcineurin by physical exercise, in hearts of mdx mice

A. Nakamura, Kunihiro Yoshida, S. Takeda, 2002, FEBS letters.

VAD with or without subsequent high-dose melphalan followed by autologous stem cell support in AL amyloidosis: Japanese experience and criteria for patient selection

J. Koyama, S. Ikeda, K. Koike, 2004, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

IgM AL amyloidosis due to B cell lymphoproliferative disorder: efficacy of high-dose melphalan followed by autologous stem cell transplantation

J. Koyama, S. Ikeda, K. Koike, 2004, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Characterization of amyloid fibril protein from a case of cerebral amyloid angiopathy showing immunohistochemical reactivity for both β protein and cystatin C

N. Yanagisawa, F. Kametani, S. Ikeda, 1992, Neuroscience Letters.

A 73-year-old patient with adult-onset type II citrullinemia successfully treated by sodium pyruvate and arginine

T. Saheki, S. Ikeda, M. Yazaki, 2013, Clinical Neurology and Neurosurgery.

Primary liver carcinoma exhibiting dual hepatocellular-biliary epithelial differentiations associated with citrin deficiency: a case report.

T. Saheki, S. Ikeda, Keiko Kobayashi, 2008, Journal of clinical gastroenterology.

Extensive loss of arterial medial smooth muscle cells and mural extracellular matrix in cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)

K. Arima, N. Ito, S. Ikeda, 2008, Neuropathology : official journal of the Japanese Society of Neuropathology.

A case of familial amyloid polyneuropathy treated with partial liver transplantation using a graft from a living related donor.

S. Kawasaki, M. Makuuchi, N. Yanagisawa, 1995, Transplantation.

Severe amyloid deposition in mammary glands of familial amyloid polyneuropathy patients

T. Tokuda, S. Ikeda, Y. Hoshii, 2007, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Familial transthyretin-type amyloid polyneuropathy in Japan: clinical and genetic heterogeneity.

G. Sobue, S. Ikeda, M. Nakazato, 2002, Neurology.

Leukoencephalopathy induced by low-dose methotrexate in a patient with rheumatoid arthritis.

S. Ikeda, Y. Shimojima, M. Matsuda, 2011, Internal medicine.

4. Vasculitis Syndrome

S. Ikeda, Y. Shimojima, 2010 .

Carpal tunnel syndrome: a common initial symptom of systemic wild-type ATTR (ATTRwt) amyloidosis

J. Koyama, S. Ikeda, T. Doden, 2016, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Serum transthyretin monomer in patients with familial amyloid polyneuropathy

T. Tokuda, F. Kametani, S. Ikeda, 2001, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

A novel nonsense mutation in the TITF-1 gene in a Japanese family with benign hereditary chorea

Kunihiro Yoshida, S. Ikeda, Katsuya Nakamura, 2012, Journal of the Neurological Sciences.

Markers for Guillain‐Barré syndrome with poor prognosis: a multi‐center study

G. Sobue, T. Kanda, M. Sonoo, 2017, Journal of the peripheral nervous system : JPNS.

Relationship between lobar intracerebral hemorrhage and leukoencephalopathy associated with cerebral amyloid angiopathy: Clinicopathological study of 64 Japanese patients

Hitoshi Takahashi, S. Ikeda, T. Oide, 2003, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Cerebral arterial pathology of CADASIL and CARASIL (Maeda syndrome)

K. Arima, N. Ito, S. Ikeda, 2003, Neuropathology : official journal of the Japanese Society of Neuropathology.

Clinical Medicine Insights: Arthritis and Musculoskeletal Disorders Phenotypes of Peripheral Blood Lymphocytes and Cytokine Expression in Polymyositis and Dermatomyositis before Treatment and after Clinical Remission

S. Ikeda, Y. Shimojima, M. Matsuda, 2022 .

ANCA-associated vasculitis with central retinal artery occlusion developing during treatment with methimazole.

S. Ikeda, M. Yazaki, M. Matsuda, 2012, Internal medicine.

Advantage of administering tacrolimus for improving the prognosis in polymyositis and dermatomyositis

S. Ikeda, Y. Shimojima, Y. Sekijima, 2018 .

Nodular lung disease with five year survival and unilateral pleural effusion in AL amyloidosis.

N. Tachibana, S. Ikeda, Y. Hoshii, 1999, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Severe generalized dystonia as a presentation of a patient with aprataxin gene mutation

T. Hashimoto, S. Tsuji, S. Ikeda, 2003, Movement disorders : official journal of the Movement Disorder Society.

Alpha-Adrenergic Receptors in Familial Amyloidotic Polyneuropathy

S. Sakoda, N. Yanagisawa, S. Tsujino, 1988 .

Quantitative evaluation of expression of iron-metabolism genes in ceruloplasmin-deficient mice.

Kunihiro Yoshida, S. Takeda, S. Ikeda, 2002, Biochimica et biophysica acta.

Marked intrafamilial phenotypic variation in a family with SOD1 C111Y mutation

A. Nakamura, S. Ohara, Kunihiro Yoshida, 2012 .

Marked intrafamilial phenotypic variation in a family with SOD1 C111Y mutation

A. Nakamura, S. Ohara, Kunihiro Yoshida, 2012, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

Chronic inflammatory demyelinating polyradiculoneuropathy with autonomic involvement

T. Hashimoto, S. Ikeda, Kanji Yamamoto, 2005, Muscle & nerve.

Neutropenia as a Complication of High-Dose Intravenous Immunoglobulin Therapy in Adult Patients With Neuroimmunologic Disorders

T. Hashimoto, S. Ikeda, M. Matsuda, 2003, Clinical neuropharmacology.

Triple a syndrome in Japan

T. Hanafusa, S. Ikeda, Katsuya Nakamura, 2013, Muscle & nerve.

Clinical Characteristics of Aged Becker Muscular Dystrophy Patients with Onset after 30 Years

A. Nakamura, J. Koyama, Kunihiro Yoshida, 1999, European Neurology.

Japanese POEMS syndrome with Thalidomide (J-POST) Trial: study protocol for a phase II/III multicentre, randomised, double-blind, placebo-controlled trial

G. Sobue, T. Kanda, J. Kira, 2015, BMJ Open.

Severe cranial nerve involvement in a patient with monoclonal anti-MAG/SGPG IgM antibody and localized hard palate amyloidosis

H. Morita, N. Yuki, S. Ikeda, 2006, Journal of the Neurological Sciences.

Cytomegalovirus-induced infectious mononucleosis-like syndrome in a rheumatoid arthritis patient treated with methotrexate and infliximab.

S. Ikeda, Y. Shimojima, M. Matsuda, 2010, Internal medicine.

Elevation of serum heat-shock protein levels in amyotrophic lateral sclerosis

A. Nakamura, Kunihiro Yoshida, S. Ikeda, 2016, Neurological Sciences.

Clinical Status and Daily-Life Activity of Patients with Amyotrophic Lateral Sclerosis in Nagano Prefecture

S. Ohara, Kunihiro Yoshida, S. Ikeda, 2007 .

Presenilin-1 exists in the axoplasm fraction in the brains of aged Down's syndrome subjects and non-demented individuals

T. Tokuda, F. Kametani, S. Ikeda, 1999, Neuroscience Letters.

Secretory form of β-amyloid precursor protein is much abundantly contained in the cerebral white matter in human brain

T. Tokuda, N. Yanagisawa, F. Kametani, 1994, Neuroscience Letters.

Type III (chronic) GM1-gangliosidosis Histochemical and ultrastructural studies of rectal biopsy

N. Yanagisawa, S. Ikeda, J. Nakayama, 1985, Journal of the Neurological Sciences.

Clinical and genetic characterization of adult‐onset leukoencephalopathy with axonal spheroids and pigmented glia associated with CSF1R mutation

Z. Wszolek, T. Kawarai, Kunihiro Yoshida, 2016, European journal of neurology.

A Case of Mitochondrial Cytopathy with a Typical Point Mutation for MELAS, Presenting with Severe Focal-Segmental Glomerulosclerosis as MainClinical Manifesta tion

S. Ikeda, Eiichiro Mawatari, Y. Sekijima, 1998, American Journal of Nephrology.

[Pathogenesis and treatment of brachial plexus neuritis].

S. Ikeda, 2013, Rinsho shinkeigaku = Clinical neurology.

Arterial thromboembolism in senile systemic amyloidosis: report of two cases

S. Ikeda, K. Tojo, Y. Sekijima, 2012, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Early cardiac involvement in senile systemic amyloidosis: a case report

H. Matsubara, S. Ikeda, M. Yazaki, 2008, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Nephrotic syndrome due to primary AL amyloidosis, successfully treated with VAD and subsequent high-dose melphalan followed by autologous peripheral blood stem cell transplantation.

S. Ikeda, K. Koike, M. Matsuda, 2003, Internal medicine.

Follow-up of three patients with a large in-frame deletion of exons 45–55 in the Duchenne muscular dystrophy (DMD) gene

A. Nakamura, J. Koyama, Kunihiro Yoshida, 2008, Journal of Clinical Neuroscience.

Glial Fibrillary Acidic Protein is Greatly Modified by Oxidative Stress in Aceruloplasminemia Brain

F. Kametani, Kunihiro Yoshida, S. Ikeda, 2002, Free radical research.

Secretory cleavage of β-amyloid precursor protein in the cerebral white matter produces amyloidogenic carboxyl-terminal fragments

T. Tokuda, N. Yanagisawa, F. Kametani, 1995, Neuroscience Letters.

Immunohistochemical and immunoelectron microscopical characterization of cerebrovascular and senile plaque amyloid in aged dogs' brains

D. Allsop, S. Ikeda, Mutsuo Takahashi, 1991, Brain Research.

Cerebral amyloid angiopathy-related hemorrhage in a middle-aged patient with Down's syndrome

S. Ikeda, Y. Sekijima, Ko-suke Naito, 2008, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Senile systemic amyloidosis in an aged savannah monkey (Cercopithecus aethiops) with tenosynovial degeneration.

S. Ikeda, Y. Une, K. Higuchi, 2010, The Journal of veterinary medical science.

Extensive brain pathology in a patient with aceruloplasminemia with a prolonged duration of illness.

H. Morita, S. Ohara, Kunihiro Yoshida, 2012, Human pathology.

Postmortem findings in a patient with cerebral amyloid angiopathy actively treated with corticosteroid

K. Arima, F. Kametani, S. Ikeda, 2012, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Transthyretin-type cerebral amyloid angiopathy in type I familial amyloid polyneuropathy

N. Yanagisawa, S. Ikeda, M. Ushiyama, 2004, Acta Neuropathologica.

Tacrolimus in refractory patients with myasthenia gravis: Coadministration and tapering of oral prednisolone

T. Tokuda, S. Ikeda, Y. Shimojima, 2006, Journal of Clinical Neuroscience.

Marked shrinkage of amyloid lymphadenopathy after an intensive chemotherapy in a patient with IgM-associated AL amyloidosis

S. Ikeda, Y. Shimojima, M. Matsuda, 2009, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Marked shrinkage of amyloid lymphadenopathy after an intensive chemotherapy in a patient with IgM-associated AL amyloidosis

S. Ikeda, Y. Shimojima, M. Matsuda, 2009, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Characterization of a transthyretin-related amyloid fibril protein from cerebral amyloid angiopathy in type I familial amyloid polyneuropathy

N. Yanagisawa, F. Kametani, S. Ikeda, 1992, Journal of the Neurological Sciences.

Unusual clinical manifestations of primary systemic AL amyloidosis: are myasthenic symptoms and dilated cardiomyopathy caused by muscular or myocardial amyloid angiopathy?

S. Ikeda, 2006, Internal medicine.

Serial CT and MRI findings in a patient with isolated angiitis of the central nervous system associated with cerebral amyloid angiopathy

T. Tokuda, Hitoshi Takahashi, S. Ikeda, 2002, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Prealbumin type cerebral amyloid angiopathy in familial amyloid polyneuropathy

N. Yanagisawa, S. Ikeda, M. Ushiyama, 1991 .

Rituximab therapy in nephrotic syndrome due to AH amyloidosis

S. Ikeda, M. Yazaki, M. Matsuda, 2009, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

AL amyloidosis manifesting as systemic lymphadenopathy

S. Ikeda, Y. Hoshii, Takuhiro Yoshida, 2008, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

A case with rheumatoid arthritis and systemic reactive AA amyloidosis showing rapid regression of amyloid deposition on gastroduodenal mucosa after a combined therapy of corticosteroid and etanercept

S. Ikeda, Y. Hoshii, Y. Shimojima, 2011, Rheumatology International.

Cyclosporin A in treatment of refractory patients with chronic inflammatory demyelinating polyradiculoneuropathy

H. Morita, S. Ikeda, M. Matsuda, 2004, Journal of the Neurological Sciences.

Intractable skin necrosis and interstitial pneumonia in amyopathic dermatomyositis, successfully treated with cyclosporin A.

T. Hashimoto, S. Ikeda, Y. Shimojima, 2003, Internal medicine.

Adult onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) and Nasu-Hakola disease: Lesion staging and dynamic changes of axons and microglial subsets

J. Satoh, H. Akiyama, S. Terada, 2017, Journal of the Neurological Sciences.

Risk factors for hospital-acquired bacteremia.

K. Kubo, S. Ikeda, Toshiro Suzuki, 2005, Internal medicine.

Complete neurological recovery of an adult patient with type II citrullinemia after living related partial liver transplantation.

S. Kawasaki, M. Makuuchi, N. Yanagisawa, 1996, Transplantation.

Transthyretin‐derived amyloid deposition on the gastric mucosa in domino recipients of familial amyloid polyneuropathy liver

S. Ikeda, M. Yazaki, S. Miyagawa, 2007, Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society.

Size variance of motor evoked potential at initiation of voluntary contraction in palsy of conversion disorder

H. Morita, S. Ikeda, N. Amano, 2008, Psychiatry and clinical neurosciences.

Cerebral hemorrhage in Fabry's disease

Y. Fukushima, F. Endo, S. Ikeda, 2010, Journal of Human Genetics.

Postmortem pathological findings in a Japanese patient with familial amyloidosis, Finnish type (FAF)

N. Yanagisawa, S. Ikeda, C. Maury, 1996 .

Huntington’s disease with onset ages greater than 60 years

Y. Fukushima, Kunihiro Yoshida, S. Ikeda, 2007 .

Nephrotic syndrome due to primary systemic AL amyloidosis, successfully treated with VAD (vincristine, doxorubicin and dexamethasone) alone.

S. Ikeda, Takuhiro Yoshida, Y. Shimojima, 2008, Internal medicine.

Evaluation of intensive chemotherapy in AL amyloidosis: usefulness of flow cytometric analysis of plasma cells in bone marrow

S. Ikeda, K. Koike, Y. Shimojima, 2003, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Rituximab therapy in chronic inflammatory demyelinating polyradiculoneuropathy with anti-SGPG IgM antibody

H. Morita, T. Hashimoto, N. Yuki, 2006, Journal of Clinical Neuroscience.

Effective Use of Calcineurin Inhibitor in Combination Therapy for Interstitial Lung Disease in Patients With Dermatomyositis and Polymyositis

S. Ikeda, Y. Shimojima, M. Matsuda, 2017, Journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases.

Coadministration of tacrolimus with corticosteroid accelerates recovery in refractory patients with polymyositis/ dermatomyositis: a retrospective study

S. Ikeda, Y. Shimojima, M. Matsuda, 2012, BMC Musculoskeletal Disorders.

Clinical Medicine Insights: Arthritis and Musculoskeletal Disorders Coadministration of Cyclosporin a with Prednisolone in Acute Interstitial Pneumonia Complicating Polymyositis/dermatomyositis

S. Ikeda, Y. Shimojima, M. Matsuda, 2022 .

Flow cytometric analysis of lymphocyte subpopulations and TH1/TH2 balance in patients with polymyositis and dermatomyositis.

T. Sumida, S. Ikeda, Y. Shimojima, 2008, Internal medicine.

Phenotypical analysis of lymphocytes using flow cytometry in dermatomyositis with and without interstitial pneumonia

S. Ikeda, Takuhiro Yoshida, Y. Shimojima, 2006 .

Nonepisodic angioedema with eosinophilia: a report of two cases and a review of the literature

A. Nakamura, S. Ikeda, M. Matsuda, 2006, Clinical Rheumatology.

Peripheral sympathetic nerve dysfunction in adolescent Japanese girls following immunization with the human papillomavirus vaccine.

S. Ikeda, A. Hineno, S. Nakane, 2014, Internal medicine.

Marked biochemical difference in amyloid proportion between intra- and extraocular tissues in a liver-transplanted patient with hereditary ATTR amyloidosis

F. Kametani, S. Ikeda, M. Yazaki, 2017, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Immunogold labeling of cerebrovascular and neuritic plaque amyloid fibrils in Alzheimer's disease with an anti-beta protein monoclonal antibody.

G. Glenner, D. Allsop, S. Ikeda, 1987, Laboratory investigation; a journal of technical methods and pathology.

Gastrointestinal amyloid deposition in familial amyloid polyneuropathy

N. Yanagisawa, S. Ikeda, H. Makishita, 1982, Neurology.

Clinical and pathological studies of cardiac amyloidosis in transthyretin type familial amyloid polyneuropathy

J. Koyama, S. Ikeda, M. Nakazato, 2003, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Sjögren syndrome-related plasma cell disorder and multifocal nodular AL amyloidosis: clinical picture and pathological findings

S. Ikeda, Y. Hoshii, K. Matsuo, 2019, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Seronegative Sjögren syndrome with asymptomatic autoimmune sclerosing pancreatitis

S. Ikeda, S. Kawa, T. Uehara, 2007, Clinical Rheumatology.

[Dropped head sign and tongue atrophy in systemic sclerosis-associated myopathy: a case report].

S. Ikeda, Y. Shimojima, M. Matsuda, 2010, Rinsho shinkeigaku = Clinical neurology.

Semiquantitative estimation of severity of immunoreactive lesions in the cases with Down ' s syndrome

N. Yanagisawa, F. Kametani, D. Allsop, 2006 .

EARLY SENILE PLAQUES IN DOWN'S SYNDROME BRAINS SHOW A CLOSE RELATIONSHIP WITH CELL BODIES OF NEURONS

D. Mann, D. Allsop, S. Ikeda, 1989, Neuropathology and applied neurobiology.

Immunohistochemical evidence for the derivation of a peptide ligand from the amyloid beta-protein precursor of Alzheimer disease.

G. Glenner, D. Allsop, S. Ikeda, 1988, Proceedings of the National Academy of Sciences of the United States of America.

Characterization of deletion breakpoints in patients with dystrophinopathy carrying a deletion of exons 45–55 of the Duchenne muscular dystrophy (DMD) gene

A. Nakamura, Kunihiro Yoshida, S. Takeda, 2009, Journal of Human Genetics.

Pravastatin at 10 mg/day does not decrease plasma levels of either amyloid-beta (Abeta) 40 or Abeta 42 in humans.

T. Tokuda, S. Ikeda, K. Ishii, 2003, Neuroscience letters.

Anti-neuronal autoantibody in Hashimoto's encephalopathy: neuropathological, immunohistochemical, and biochemical analysis of two patients

T. Hashimoto, T. Tokuda, S. Ohara, 2004, Journal of the Neurological Sciences.

Spinal nerve root hypertrophy on MRI: clinical significance in the diagnosis of chronic inflammatory demyelinating polyradiculoneuropathy.

H. Morita, S. Ikeda, H. Ueda, 2008, Internal medicine.

A Young Man with Anti-NMDAR Encephalitis following Guillain-Barré Syndrome

H. Morita, S. Ikeda, K. Tojo, 2011, Case Reports in Neurology.

Expression of various glutamate receptors including N-methyl-D-aspartate receptor (NMDAR) in an ovarian teratoma removed from a young woman with anti-NMDAR encephalitis.

K. Arima, N. Tachibana, S. Ikeda, 2010, Internal medicine.

Peripheral Sympathetic Nerve Dysfunction in Adolescent Japanese Girls Following Immunization with the Human Papillomavirus Vaccine.

S. Ikeda, T. Kinoshita, 2015, Internal medicine.

Pathologic basis of the preferential thinning of thecorpus callosum in adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP)

Kunihiro Yoshida, S. Ikeda, M. Yamada, 2021, eNeurologicalSci.

Synovial deposition of wild-type transthyretin-derived amyloid in knee joint osteoarthritis patients

S. Ikeda, M. Yazaki, M. Matsuda, 2013, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Adult onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) and Nasu-Hakola disease: Lesion staging and dynamic changes of axons and microglial subsets

J. Satoh, S. Ikeda, K. Oyanagi, 2017, Journal of the Neurological Sciences.

Astrocytic Deformity and Globular Structures Are Characteristic of the Brains of Patients with Aceruloplasminemia

K. Arima, Takeo Kato, S. Ohara, 2002, Journal of neuropathology and experimental neurology.

Living donor liver transplantation using a graft with periportal fibrosis

M. Makuuchi, S. Ikeda, T. Takayama, 2015, Hepatology research : the official journal of the Japan Society of Hepatology.

Diagnostic criteria for adult‐onset leukoencephalopathy with axonal spheroids and pigmented glia due to CSF1R mutation

Z. Wszolek, T. Kawarai, S. Ikeda, 2018, European journal of neurology.

Corpus callosum atrophy in patients with hereditary diffuse leukoencephalopathy with neuroaxonal spheroids: an MRI-based study.

J. Kira, N. Araki, Kunihiro Yoshida, 2014, Internal medicine.

Early involvement of the corpus callosum in a patient with hereditary diffuse leukoencephalopathy with spheroids carrying the de novo K793T mutation of CSF1R.

Kunihiro Yoshida, S. Ikeda, K. Fukushima, 2013, Internal medicine.

Hereditary diffuse leukoencephalopathy with axonal spheroids caused by R782H mutation in CSF1R: Case report

T. Hashimoto, Kunihiro Yoshida, S. Ikeda, 2012, Journal of the Neurological Sciences.

Amyloid fibril protein nomenclature: 2010 recommendations from the nomenclature committee of the International Society of Amyloidosis

M. Benson, M. Saraiva, S. Ikeda, 2010, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

[Diagnosis and treatment in systemic amyloidosis].

S. Ikeda, 2008, Rinsho byori. The Japanese journal of clinical pathology.

Liver Transplantation: An Effective Treatment For Familial ATTR Amyloidosis

C. Masters, M. Benson, M. Saraiva, 2002, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Ceruloplasmin Protects Against Rotenone-Induced Oxidative Stress and Neurotoxicity

Kunihiro Yoshida, S. Ikeda, A. Hineno, 2011, Neurochemical Research.

Increased vulnerability to rotenone-induced neurotoxicity in ceruloplasmin-deficient mice

Kunihiro Yoshida, S. Ikeda, A. Hineno, 2008, Neuroscience Letters.

Peripheral nerve pathological findings in familial amyloid polyneuropathy: A correlative study of proximal sciatic nerve and sural nerve lesions

N. Yanagisawa, S. Ikeda, H. Powell, 1989, Annals of neurology.

AL amyloidosis with spontaneous hepatic rupture: successful treatment by transcatheter hepatic artery embolization

S. Kawakami, S. Ikeda, M. Kadoya, 2008, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Recurrent cerebral embolism in a familial amyloid polyneuropathy patient who received partial liver transplantation from a living donor.

S. Kawasaki, S. Ikeda, Y. Takei, 2001, Internal medicine.

[Lower urinary tract dysfunction and neuropathological findings of the neural circuits controlling micturition in familial amyotrophic lateral sclerosis with L106V mutation in the SOD1 gene].

A. Nakamura, Kunihiro Yoshida, S. Ikeda, 2016, Rinsho shinkeigaku = Clinical neurology.

Superficial siderosis associated with aceruloplasminemia. Case report.

A. Kakita, S. Ohara, Kunihiro Yoshida, 2014, Journal of the neurological sciences.

Increase in incidence of elderly-onset patients with myasthenia gravis in Nagano Prefecture, Japan.

A. Nakamura, H. Morita, S. Ikeda, 2005, Internal medicine.

Multifocal Fibrosclerosis with Hypertrophic Pachymeningitis and a Soft Tissue Mass around the Thoracic Vertebral Bodies: A Case Report with Review of the Literature.

S. Ikeda, T. Uehara, Y. Shimojima, 2015, Internal medicine.

Liver Transplantation Is a Potential Treatment Option for Systemic Light Chain Amyloidosis Patients with Dominant Hepatic Involvement: A Case Report and Analytical Review of the Literature.

M. Makuuchi, S. Ikeda, A. Ueno, 2016, Internal medicine.

Massive mesenteric edema in a patient with type I hereditary angioedema

T. Hashimoto, F. Otsuka, S. Ikeda, 2005, Modern rheumatology.

CPPD crystal deposition disease of the cervical spine: A common cause of acute neck pain encountered in the neurology department

S. Ikeda, Takuhiro Yoshida, Y. Sekijima, 2010, Journal of the Neurological Sciences.

Amyloid Fibril Protein Nomenclature - 2002

C. Masters, M. Benson, M. Saraiva, 2002, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Calciphylaxis as a Catastrophic Complication in a Patient with POEMS Syndrome

Kunihiro Yoshida, S. Ikeda, Y. Shimojima, 2009, Case Reports in Neurology.

Clinicopathological Studies on Nephropathy of Familial Amyloid Polyneuropathy in Japan

S. Ikeda, H. Shigematsu, H. Oguchi, 1988 .

Clinical and Pathological Studies of Familial Amyloid Polyneuropathy (FAP), with Special Reference to Nephropathy and Cardiopathy

N. Ito, N. Yanagisawa, S. Ikeda, 1986 .

Upper limb neuropathy such as carpal tunnel syndrome as an initial manifestation of ATTR Val30Met familial amyloid polyneuropathy

H. Morita, S. Ikeda, K. Tojo, 2010, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Clinicopathologic and genetic features of early- and late-onset FAP type I (FAP ATTR Val30Met) in Japan

G. Sobue, S. Ikeda, M. Nakazato, 2003, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Vagus nerve and celiac ganglion lesions in generalized amyloidosis A correlative study of familial amyloid polyneuropathy and AL-amyloidosis

N. Ito, N. Yanagisawa, S. Ikeda, 1987, Journal of the Neurological Sciences.

Amyloidogenic transthyretin Val30Met homozygote showing unusually early‐onset familial amyloid polyneuropathy

S. Ikeda, M. Yazaki, K. Tojo, 2008, Muscle & nerve.

Amyloid neuropathy and autonomic dysfunction

S. Ikeda, 2022, Neurology and Clinical Neuroscience.

Localized amyloidogenic immunoglobulin light chain-derived amyloidosis in a young boy and an adolescent girl

S. Ikeda, 2017, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Regression of localized ureter amyloidosis after treatment with steroids suggested by Tc-99 m pyrophosphate scintigraphy

S. Ikeda, Y. Sekijima, J. Ikeda, 2015, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Amyloid: Toward terminology clarification Report from the Nomenclature Committee of the International Society of Amyloidosis

Giampaolo Merlini, Colin L Masters, Shu-Ichi Ikeda, 2005, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Fasciitis in mixed connective tissue disease successfully treated with high-dose intravenous immunoglobulin.

S. Ikeda, K. Tabata, M. Matsuda, 2003, Internal medicine.

Reversible extensive leukoencephalopathy in Sweet disease: A case report

H. Morita, Kunihiro Yoshida, S. Ikeda, 2008, Journal of the Neurological Sciences.

Safety and efficacy of thalidomide in patients with POEMS syndrome: a multicentre, randomised, double-blind, placebo-controlled trial

G. Sobue, T. Kanda, J. Kira, 2016, The Lancet Neurology.

Brain SPECT with 123I-IMP for the early diagnosis of Creutzfeldt–Jakob disease

S. Ikeda, K. Tabata, M. Matsuda, 2001, Journal of the Neurological Sciences.

Three patients with isolated adrenocorticotropin deficiency presenting with neuroleptic malignant syndrome-like symptoms.

S. Ikeda, M. Okada, Y. Sekijima, 2001, Internal medicine.

Recurrent steroid-responsive trismus and painful ophthalmoplegia

S. Ikeda, N. Hanyu, M. Yamazaki, 1999, Journal of the Neurological Sciences.

Static balance impairment and its change after pallidotomy in Parkinson's disease

T. Hashimoto, S. Ikeda, N. Hagiwara, 2004, Movement disorders : official journal of the Movement Disorder Society.

A mutation in the ceruloplasmin gene is associated with systemic hemosiderosis in humans

Akinori Nakamura, Kunihiro Yoshida, Norikazu Shimizu, 1995, Nature Genetics.

Relation between changes in long-latency stretch reflexes and muscle stiffness in Parkinson's disease – comparison before and after unilateral pallidotomy

T. Hashimoto, R. Hayashi, S. Ikeda, 2001, Clinical Neurophysiology.

Two Japanese cases with aspartylglycosaminuria: clinical and morphological features

N. Yanagisawa, Kunihiro Yoshida, S. Ikeda, 1991, Clinical genetics.

ULTRASTRUCTURAL FINDINGS OF RECTAL AND SKIN BIOPSIES IN ADULT GM1‐GANGLIOSIDOSIS

N. Yanagisawa, S. Ikeda, K. Kondo, 1986, Acta pathologica japonica.

Adult or late-onset triple A syndrome Case report and literature review

H. Morita, Kunihiro Yoshida, S. Ikeda, 2010, Journal of the Neurological Sciences.

Herpes simplex virus type-1 meningoencephalitis showing disseminated cortical lesions.

T. Hashimoto, S. Ikeda, Ko-suke Naito, 2007, Internal medicine.

Efficacy of tacrolimus in treatment of polymyositis associated with myasthenia gravis

Kunihiro Yoshida, S. Ikeda, Y. Shimojima, 2004, Clinical Rheumatology.

Association of HTRA1 mutations and familial ischemic cerebral small-vessel disease.

S. Tsuji, K. Arima, Tadashi Yamamoto, 2009, The New England journal of medicine.

Adult GM1‐gangliosidosis

N. Yanagisawa, S. Ikeda, T. Nakano, 1985, Neurology.

Adult fucosidosis

N. Yanagisawa, S. Ikeda, F. Murata, 1984, Neurology.

Late-onset spastic ataxia phenotype in a patient with a homozygous DDHD2 mutation

S. Tsuji, N. Matsumoto, M. Shiina, 2014, Scientific Reports.

Extrinsic and Intrinsic Nerve Lesions of the Intestine in Type I Familial Amyloid Polyneuropathy

N. Yanagisawa, S. Ikeda, M. Yazawa, 1991 .

Activation and localization of matrix metalloproteinase-2 and -9 in the skeletal muscle of the muscular dystrophy dog (CXMDJ)

A. Nakamura, Kunihiro Yoshida, H. Ueda, 2007, BMC musculoskeletal disorders.

Distinctive clinicopathological features of 2 large families with amyotrophic lateral sclerosis having L106V mutation in SOD1 gene

A. Nakamura, Kunihiro Yoshida, S. Ikeda, 2012, Journal of the Neurological Sciences.

Late-onset autosomal recessive limb-girdle muscular dystrophy with rimmed vacuoles

A. Nakamura, Kunihiro Yoshida, S. Ikeda, 2004, Clinical Neurology and Neurosurgery.

Coexistence of Copper in the Iron-Rich Particles of Aceruloplasminemia Brain

S. Ohara, T. Ishikawa, Kunihiro Yoshida, 2016, Biological Trace Element Research.

α‐Synuclein implicated in Parkinson's disease is present in extracellular biological fluids, including human plasma

M. Cookson, J. Hardy, D. Mann, 2003, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Pure red cell aplasia developing after treatment of pleural recurrence of thymoma, successfully treated with cyclosporin A but not with tacrolimus.

S. Ikeda, M. Yazaki, T. Gono, 2006, Internal medicine.

Expression of N-methyl-D-aspartate receptor subunits in the bovine ovum: ova as a potential source of autoantigens causing anti-NMDAR encephalitis.

F. Kametani, N. Tachibana, S. Ikeda, 2015, The Tohoku journal of experimental medicine.

Spinal intradural extramedullary cavernous angioma presenting with superficial siderosis and hydrocephalus: a case report and review of the literature.

K. Hongo, S. Ikeda, T. Uehara, 2014, Internal medicine.

Postmortem findings in a familial amyloid polyneuropathy patient with homozygosity of the mutant Val30Met transthyretin gene

S. Ikeda, Y. Takei, K. Katayanagi, 2004, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Hypertrophic Pachymeningitis as an Early Manifestation of Relapsing Polychondritis: Case Report and Review of the Literature

S. Ikeda, Katsuya Nakamura, Y. Shimojima, 2016, Case Reports in Neurology.

Biopsy-proven tuberculous meningitis mimicking CNS sarcoidosis.

Kunihiro Yoshida, S. Ikeda, M. Yazaki, 2007, Internal medicine.

Peripheral nerve function in patients with familial amyloid polyneuropathy after liver transplantation

S. Kawasaki, H. Morita, T. Hashimoto, 2003, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Partial-Liver Transplantation To Treat Familial Amyloid Polyneuropathy: Follow-up of 11 Patients

S. Kawasaki, S. Ikeda, Y. Takei, 1999, Annals of Internal Medicine.

Peripheral Nerves Regenerated in Familial Amyloid Polyneuropathy after Liver Transplantation

S. Kawasaki, N. Yanagisawa, S. Ikeda, 1997, Annals of Internal Medicine.

Feasibility of auxiliary partial orthotopic liver transplantation from living donors for patients with adult‐onset type II citrullinemia

T. Tokuda, T. Saheki, S. Ikeda, 2004, Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society.

The pathological and biochemical identification of possible seed‐lesions of transmitted transthyretin amyloidosis after domino liver transplantation

F. Kametani, S. Ikeda, M. Yazaki, 2016, The journal of pathology. Clinical research.

[Liver transplantation for familial amyloidosis].

S. Ikeda, 2006, Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine.

Nodular cutaneous amyloidosis and carpal tDnnel syndrome due to the amyloidogenic transthyretin His 114 variant

T. Tokuda, H. Mochizuki, S. Ikeda, 2001, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Clinical and pathological findings of non-Val30Met TTR type familial amyloid polyneuropathy in Japan

T. Tokuda, S. Ikeda, Y. Ando, 2003, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Liver transplantation as treatment for neurological disorders

S. Ikeda, Y. Takei, Y. Hashikura, 2003, Expert review of neurotherapeutics.

[The 40th scientific meeting: perspectives of internal medicine; present situation and future extension of organ transplantation in Japan; 7. Liver transplanation for hereditary diseases].

S. Ikeda, 2013, Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine.

Value of renal biopsy in the prognosis of liver transplantation in familial amyloid polyneuropathy ATTR Val30Met patients

S. Ikeda, Y. Takei, K. Oguchi, 2006, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

S. Kawasaki, S. Ikeda, Y. Takei, 2001 .

Diagnostic value of abdominal fat tissue aspirate in familial amyloid polyneuropathy

N. Yanagisawa, S. Ikeda, M. Nakazato, 1987, Journal of the Neurological Sciences.

Isolated autonomic failure without evident somatic polyneuropathy in AL amyloidosis

S. Ikeda, S. Kuwabara, K. Sano, 2014, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

A novel RNA splice site mutation in the C1 inhibitor gene of a patient with type I hereditary angioedema.

T. Hashimoto, F. Otsuka, S. Ikeda, 2004, Internal medicine.

Exome sequencing reveals a homozygous SYT14 mutation in adult-onset, autosomal-recessive spinocerebellar ataxia with psychomotor retardation.

H. Morita, Y. Kuroiwa, S. Tsuji, 2011, American journal of human genetics.

Muscle CT scan findings in McLeod syndrome and chorea‐acanthocytosis

N. Tachibana, S. Ikeda, K. Tabata, 2000, Muscle and Nerve.

Klüver–Bucy syndrome following status epilepticus associated with hepatic encephalopathy

T. Hashimoto, S. Ikeda, Ko-suke Naito, 2008, Epilepsy & Behavior.

Japanese family with an autosomal dominant chromosome instability syndrome: a new neurodegenerative disease?

Y. Fukushima, T. Tokuda, S. Ohara, 2000, American journal of medical genetics.

Repurposing diflunisal for familial amyloid polyneuropathy: a randomized clinical trial.

E. Nordh, M. Skinner, D. Seldin, 2013, JAMA.

Abnormal activity in the globus pallidus in off‐period dystonia

T. Hashimoto, S. Ikeda, S. Katai, 2001, Annals of neurology.

Sarcoidosis with high serum levels of vascular endothelial growth factor (VEGF), showing RS3PE-like symptoms in extremities

S. Ikeda, M. Matsuda, Kanji Yamamoto, 2004, Clinical Rheumatology.

Osmotic demyelination syndrome: reversible MRI findings in bilateral cortical lesions.

S. Ikeda, Y. Takei, C. Akahane, 2003, Internal medicine.

Autoantibodies against Autonomic Nerve Receptors in Adolescent Japanese Girls after Immunization with Human Papillomavirus Vaccine

Y. Shoenfeld, C. Scheibenbogen, S. Ikeda, 2019 .

Clinical patterns and rectal biopsy

N. Yanagisawa, S. Ikeda, T. Nakano, 2006 .

Nationwide survey on predictive genetic testing for late-onset, incurable neurological diseases in Japan

Y. Fukushima, Kunihiro Yoshida, S. Ikeda, 2007, Journal of Human Genetics.

Haplotype analysis in gelsoiin‐related amyloidosis reveals independent origin of identical mutation (G654A) of gelsolin in Finland and Japan

T. Paunio, L. Peltonen, J. Weissenbach, 1995, Human mutation.

Transthyretin Tyr69-to-Ile mutation (doublenucleotide substitution in codon 69) in a Japanese familial amyloidosis patient with cardiomyopathy and carpal tunnel syndrome

T. Tokuda, S. Ikeda, M. Yazaki, 2003, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Choroidal vascular lesions identified by ICG angiography in a case of familial amyloidotic polyneuropathy.

S. Ichinose, Y. Eishi, M. Mochizuki, 2003, Japanese journal of ophthalmology.

Hereditary renal amyloidosis caused by a heterozygous G654A gelsolin mutation: a report of two cases

S. Kiuru-Enari, S. Ikeda, T. Hosoya, 2013, Clinical kidney journal.

Diagnosis of familial amyloidotic polyneuropathy

N. Yanagisawa, S. Tsujino, S. Ikeda, 1987, Neurology.

Hypersomnia and low CSF hypocretin-1 (orexin-A) concentration in a patient with multiple sclerosis showing bilateral hypothalamic lesions.

T. Hashimoto, S. Ikeda, T. Kanbayashi, 2003, Internal medicine.

A patient with severe renal amyloidosis associated with an immunoglobulin γ-heavy chain fragment

T. Tokuda, F. Kametani, S. Ikeda, 2004 .

AH amyloidosis associated with an immunoglobulin heavy chain variable region (VH1) fragment: a case report

F. Kametani, S. Ikeda, M. Yazaki, 2008, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

AH amyloidosis associated with lymphoplasmacytic lymphoma secreting a monoclonal gamma heavy chain carrying an unusual truncated D segment.

N. Ito, F. Kametani, S. Ikeda, 2006, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Neuronal activity in the globus pallidus in chorea caused by striatal lacunar infarction

H. Morita, T. Hashimoto, S. Ikeda, 2001, Annals of neurology.

Liver dysfunction and thrombocytopenia diagnosed as intravascular large B-cell lymphoma using a timely and accurate transjugular liver biopsy.

S. Ikeda, T. Matsushita, M. Kadoya, 2013, Internal medicine.

Recurrent Cerebral Infarctions caused by Intravascular Lymphoma Diagnosed by Brain Biopsy : A Case Report

K. Hongo, S. Ikeda, T. Yako, 2012 .

Patient with adult‐onset type II citrullinemia beginning 2 years after operation for duodenal malignant somatostatinoma: Indication for liver transplantation

M. Makuuchi, Y. Iwasaki, S. Ikeda, 2013, Hepatology research : the official journal of the Japan Society of Hepatology.

Long-term Follow-up Studies of Posterior Fusion of the Upper Spine in Rheumatoid Arthritis

S. Ikeda, J. Mochida, Shin-ya Kobayashi, 2005 .

Increased lipid peroxidation in the brains of aceruloplasminemia patients

A. Nakamura, T. Tokuda, Masahiro Kato, 2000, Journal of the Neurological Sciences.

Reactive arthritis due to asymptomatic infection of Chlamydia trachomatis.

S. Ikeda, M. Yazaki, Y. Shimojima, 2005, Internal medicine.

On the occurrence of neuronal sprouting in the frontal cortex of a patient with Down’s syndrome

S. Ohara, S. Ikeda, Masashige Tsukada, 1999, Acta Neuropathologica.

Early senile plaques in Alzheimer's disease demonstrated by histochemistry, immunocytochemistry, and electron microscopy.

G. Glenner, N. Yanagisawa, D. Allsop, 1990, Human pathology.

Lupus erythematosus profundus (lupus panniculitis) induced by interferon-β in a multiple sclerosis patient

S. Ikeda, H. Murata, Y. Shimojima, 2007, Journal of Clinical Neuroscience.

Congenital fibrosis of the extraocular muscles (CFEOM) syndrome associated with progressive cerebellar ataxia

G. Sobue, Kunihiro Yoshida, S. Ikeda, 2007, American journal of medical genetics. Part A.

Laryngo-tracheo-bronchial amyloidosis presenting severe airway stenosis.

K. Kubo, S. Ikeda, M. Yasuo, 2006, Internal medicine.

Soluble Aβ homeostasis in AD and DS: impairment of anti-amyloidogenic protection by lipoproteins

S. Hirai, T. Tokuda, E. Matsubara, 2004, Neurobiology of Aging.

Plasma Levels of amyloid β proteins Aβ1–40 and Aβ1–42(43) are elevated in Down's syndrome

T. Tokuda, N. Yanagisawa, S. Ikeda, 1997 .

EEG–EMG polygraphic study of dystonia and myoclonus in a case of Creutzfeldt–Jakob disease☆

T. Hashimoto, S. Ikeda, W. Ishii, 2015, Epilepsy & Behavior Case Reports.

Henoch–Schönlein purpura nephritis complicated by reversible posterior leukoencephalopathy syndrome

S. Ikeda, D. Sasayama, Y. Shimojima, 2007, Clinical Rheumatology.

Periodic alternating nystagmus and rebound nystagmus in spinocerebellar ataxia type 6

T. Hashimoto, Kunihiro Yoshida, S. Ikeda, 2003, Movement disorders : official journal of the Movement Disorder Society.

Treatment of Hypophonia With Collagen Vocal Cord Augmentation in Patients With Parkinsonism

T. Hashimoto, S. Tsuji, S. Ikeda, 2003 .

Prevalence of Dementia ofAlzheimer Type and Apolipoprotein EPhenotypes in Aged Patients withDown’s Syndrome

T. Tokuda, N. Yanagisawa, S. Ikeda, 1998, European Neurology.

Adult GM1 gangliosidosis

Kenji Kawaguchi, N. Yanagisawa, Kunihiro Yoshida, 1994, Neurology.

Coexistence of hemidystonia and hemiballism in a diabetic patient with striatal hyperintensity on T1-weighted MRI

T. Hashimoto, S. Ikeda, K. Tabata, 2001, Journal of Neurology.

Natural History of Spinocerebellar Ataxia Type 31: a 4-Year Prospective Study

H. Morita, S. Ohara, Kunihiro Yoshida, 2017, The Cerebellum.

Clinical assessment of standing and gait in ataxic patients using a triaxial accelerometer

Akinori Nakamura, Hirokazu Genno, Kunihiro Yoshida, 2015, Cerebellum & Ataxias.

An 85-year-old case with Hashimoto's encephalopathy, showing spontaneous complete remission.

S. Ikeda, Takuhiro Yoshida, Y. Shimojima, 2007, Internal medicine.

A variant of Gerstmann-Sträussler-Scheinker disease with ß -protein epitopes and dystrophic neurites in the peripheral regions of PrP -immunoreactive amyloid plaques

G. Glenner, N. Yanagisawa, D. Allsop, 1991 .

Matrix metalloproteinase-2 ablation in dystrophin-deficient mdx muscles reduces angiogenesis resulting in impaired growth of regenerated muscle fibers.

A. Nakamura, Kunihiro Yoshida, S. Takeda, 2011, Human molecular genetics.

Clinical and serial MRI findings of a sialidosis type I patient with a novel missense mutation in the NEU1 gene.

S. Ikeda, E. Nanba, Katsuya Nakamura, 2013, Internal medicine.

Nationwide Survey of 741 Patients with Systemic Amyloid Light-chain Amyloidosis in Japan

S. Ikeda, Y. Ando, M. Yazaki, 2017, Internal medicine.

A primer of amyloid nomenclature

C. Masters, M. Benson, M. Saraiva, 2007, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

High prevalence of wild-type transthyretin deposition in patients with idiopathic carpal tunnel syndrome: a common cause of carpal tunnel syndrome in the elderly.

T. Imaeda, S. Ikeda, H. Kato, 2011, Human pathology.

Regression of gastroduodenal amyloid deposition in systemic AL amyloidosis after intensive chemotherapies

S. Ikeda, M. Matsuda, Ayako Tsuchiya-Suzuki, 2011, British journal of haematology.

Recurrent gastric hemorrhaging with large submucosal hematomas in a patient with primary AL systemic amyloidosis: endoscopic and histopathological findings.

S. Ikeda, Y. Hoshii, K. Mukawa, 2004, Internal medicine.

Successful treatment with infliximab and low-dose methotrexate in a Japanese patient with familial Mediterranean fever.

A. Nakamura, S. Ikeda, Y. Shimojima, 2007, Internal medicine.

Adalimumab Monotherapy in a Patient with Psoriatic Arthritis Associated with Chronic Renal Failure on Hemodialysis: A Case Report and Literature Review

S. Ikeda, Y. Shimojima, M. Matsuda, 2012, Clinical medicine insights. Case reports.

Painful ophthalmoplegia due to inflammation of the cavernous sinus in a patient with familial Mediterranean fever

A. Nakamura, S. Ikeda, M. Yazaki, 2017 .

Successful treatment of fulminant Wilson's disease without liver transplantation

S. Ikeda, K. Koike, K. Sano, 2014, Pediatrics international : official journal of the Japan Pediatric Society.

Fatal acute pancreatitis with cystic formation in reactive systemic AA amyloidosis secondary to rheumatoid arthritis.

S. Ikeda, M. Kadoya, M. Matsuda, 2003, Internal medicine.

Bilateral localized amyloidosis of the ureters: clinicopathology and therapeutic approaches in two cases

S. Ikeda, Y. Hoshii, T. Ishihara, 2004, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Protein-losing Gastroenteropathy Related to Mixed Connective Tissue Disease: A Case Report of a Successful Outcome and Literature Review

Yuya Kobayashi, S. Ikeda, Y. Shimojima, 2017, Internal medicine.

[Two patients with different types of vasculitic neuropathy--a comparison between cutaneous polyarteritis nodosa and nonsystemic vasculitic neuropathy].

T. Hashimoto, S. Ikeda, Y. Sekijima, 2003, Rinsho shinkeigaku = Clinical neurology.

Secretory form of Alzheimer amyloid precursor protein 695 in human brain lacks beta/A4 amyloid immunoreactivity.

H. E. Kennedy, K. Tanaka, F. Kametani, 1993, Biochemical and biophysical research communications.

Pravastatin at 10 mg/day does not decrease plasma levels of either amyloid-β (Aβ) 40 or Aβ 42 in humans

T. Tokuda, S. Ikeda, K. Ishii, 2003, Neuroscience Letters.

Energetic Characteristics of the New Transthyretin Variant A25T May Explain Its Atypical Central Nervous System Pathology

T. Tokuda, J. Kelly, Y. Shimizu, 2003, Laboratory Investigation.

Stereotyped stepping associated with lesions in the bilateral medial frontoparietal cortices

A. Nakamura, T. Hashimoto, S. Ikeda, 2001, Neurology.

Suspected adverse effects after human papillomavirus vaccination: a temporal relationship

S. Ikeda, K. Ozawa, A. Hineno, 2018, Immunologic research.

Suspected Adverse Effects After Human Papillomavirus Vaccination: A Temporal Relationship Between Vaccine Administration and the Appearance of Symptoms in Japan

S. Ikeda, K. Ozawa, A. Hineno, 2017, Drug Safety.

Plasma levels of amyloid β proteins did not differ between subjects taking statins and those not taking statins

H. Morita, T. Tokuda, S. Ikeda, 2001, Annals of neurology.

Senile systemic amyloidosis starting as bilateral carpal and left ulnar tunnel syndrome.

T. Tokuda, S. Saitoh, S. Ikeda, 2003, Internal medicine.

Thorn-shaped astrocytes: possibly secondarily induced tau-positive glial fibrillary tangles

T. Tokuda, H. Akiyama, S. Ikeda, 2004, Acta Neuropathologica.

Human Papillomavirus (HPV) Vaccination: Just the Facts.

S. Ikeda, T. Kinoshita, 2015, Internal medicine.

Familial amyloid polyneuropathy in Taiwan: Identification of transthyretin variant (Leu55 → Pro)

N. Yanagisawa, Kunihiro Yoshida, S. Ikeda, 1994, Muscle & nerve.

Systemic reactive amyloidosis associated with Castleman's disease: serial changes of the concentrations of acute phase serum amyloid A and interleukin 6 in serum.

S. Kawasaki, S. Ikeda, Y. Hoshii, 1997, Journal of clinical pathology.

A 67‐Year‐Old Man with Leg Weakness and Hypertrophic Cardiomyopathy

I. Nishino, S. Ikeda, Yuji Takahashi, 2020, Brain pathology.

Distinctive features of degenerating Purkinje cells in spinocerebellar ataxia type 31

Kunihiro Yoshida, S. Ikeda, K. Oyanagi, 2013, Neuropathology (Kyoto. 1993).

Analysis of an insertion mutation in a cohort of 94 patients with spinocerebellar ataxia type 31 from Nagano, Japan

Naomichi Matsumoto, Kunihiro Yoshida, Shu-ichi Ikeda, 2010, neurogenetics.

Severity and Progression Rate of Cerebellar Ataxia in 16q-linked Autosomal Dominant Cerebellar Ataxia (16q-ADCA) in the Endemic Nagano Area of Japan

Naomichi Matsumoto, Kunihiro Yoshida, Shinji Ohara, 2009, The Cerebellum.

Shinshu Brain Resource Net

Kunihiro Yoshida, Hiroyuki Kanno, Takao Hashimoto, 2016, Neuropathology : official journal of the Japanese Society of Neuropathology.

[Autonomic dysfunction in FAP: its therapeutic effect by liver transplantation].

S. Ikeda, 2006, Rinsho shinkeigaku = Clinical neurology.

A New procedure for temporary auxiliary partial liver transplantation using living donor graft for patients with familial amyloid polyneuropathy

S. Ikeda, S. Miyagawa, T. Ikegami, 2012, Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society.

Buerger's disease manifesting nodular erythema with livedo reticularis.

S. Ikeda, M. Nose, M. Matsuda, 2007, Internal medicine.

Churg-Strauss syndrome presenting as myositis following unaccustomed exercise

T. Hashimoto, S. Ikeda, K. Higuchi, 2009, Journal of Clinical Neuroscience.

Paraneoplastic Sensorimotor Neuropathy and Encephalopathy Associated with Anti-α-Enolase Antibody in a Case of Gastric Adenocarcinoma

T. Tokuda, F. Kametani, S. Ikeda, 2004, European Neurology.

Identification of the N-Methyl-D-aspartate receptor (NMDAR)-related epitope, NR2B, in the normal human ovary: implication for the pathogenesis of anti-NMDAR encephalitis.

N. Tachibana, S. Ikeda, Yuko Saito, 2013, The Tohoku journal of experimental medicine.

[Cardiac involvement in systemic amyloidosis: myocardial scintigraphic evaluation].

S. Ikeda, M. Hongo, H. Yamada, 1985, Journal of cardiography.

Comparison of the standard and speckle tracking echocardiographic features of wild-type and mutated transthyretin cardiac amyloidoses.

J. Koyama, S. Ikeda, Uichi Ikeda, 2016, European heart journal cardiovascular Imaging.

Left ventricular deformation and torsion assessed by speckle-tracking echocardiography in patients with mutated transthyretin-associated cardiac amyloidosis and the effect of diflunisal on myocardial function☆

J. Koyama, S. Ikeda, Uichi Ikeda, 2015, International journal of cardiology. Heart & vasculature.

Cardiac positron-emission tomography images with an amyloid-specific tracer in familial transthyretin-related systemic amyloidosis.

H. Arai, M. Tashiro, N. Okamura, 2012, Circulation.

Cerebral amyloid angiopathy in posttransplant patients with hereditary ATTR amyloidosis

F. Kametani, S. Ikeda, M. Yamada, 2016, Neurology.

Clinical and radiological findings of a cerebrotendinous xanthomatosis patient with a novel p.A335V mutation in the CYP27A1 gene.

S. Ikeda, Y. Sekijima, T. Yoshinaga, 2014, Internal medicine.

Molecular analysis of the duchenne muscular dystrophy gene in patients with becker muscular dystrophy presenting with dilated cardiomyopathy

N. Yanagisawa, Kunihiro Yoshida, S. Ikeda, 1993, Muscle & nerve.

Dystonia, mental deterioration, and dyschromatosis symmetrica hereditaria in a family with ADAR1 mutation

T. Hashimoto, Kunihiro Yoshida, S. Ikeda, 2006, Movement disorders : official journal of the Movement Disorder Society.

Follow-up nationwide survey on predictive genetic testing for late-onset hereditary neurological diseases in Japan

Y. Fukushima, Kunihiro Yoshida, S. Ikeda, 2013, Journal of Human Genetics.

Comparison of the strain Doppler echocardiographic features of familial amyloid polyneuropathy (FAP) and light-chain amyloidosis.

R. Falk, J. Koyama, S. Ikeda, 2005, The American journal of cardiology.

Transthyretin Thr60Ala Appalachian-type mutation in a Japanese family with familial amyloidotic polyneuropathy

S. Yamaguchi, Shotai Kobayashi, T. Tokuda, 2002, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Effects of tafamidis treatment on transthyretin (TTR) stabilization, efficacy, and safety in Japanese patients with familial amyloid polyneuropathy (TTR-FAP) with Val30Met and non-Val30Met: A phase III, open-label study

H. Morita, K. Machii, M. Ohta, 2016, Journal of the Neurological Sciences.

Induction of AApoAII amyloidosis by various heterogeneous amyloid fibrils

S. Ikeda, M. Hosokawa, T. Matsushita, 2004, FEBS letters.

CEREBRAL AMYLOID AND ALZHEIMER'S DISEASE — EVIDENCE FOR THE DERIVATION OF A PEPTIDE LIGAND FROM THE β PROTEIN PRECURSOR

G. Glenner, D. Allsop, S. Ikeda, 1988 .

Isaacs’ syndrome associated with myasthenia gravis, showing remission after cytoreductive surgery of pleural recurrence of thymoma

T. Hashimoto, S. Ikeda, M. Yazaki, 2006, Neuromuscular Disorders.

[Survey on the attitude toward genetic testing of neurologists certified by the Japanese Society of Neurology].

Kunihiro Yoshida, S. Ikeda, T. Toda, 2013, Rinsho shinkeigaku = Clinical neurology.

[Current status of the predictive genetic testing for hereditary neurological diseases in Shinshu University Hospital].

Y. Fukushima, Kunihiro Yoshida, S. Ikeda, 2013, Rinsho shinkeigaku = Clinical neurology.

[Metabolic turn over of amyloid fibrils and post-treatment regression of amyloid deposits in systemic amyloidosis with polyneuropathy].

S. Ikeda, 2011, Rinsho shinkeigaku = Clinical neurology.

Familial amyloid polyneuropathy in Korea: The first case report with a proven ATTR Lys35Asn gene

S. Ikeda, H. Baik, Y. Takei, 2005, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Proteomic analysis of leptomeningeal amyloid fibril extracts of cerebral amyloid angiopathy (CAA) patients with or without corticosteroid therapy

F. Kametani, S. Ikeda, 2013, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Successful Treatment with Alpha-Interferon of a Patient with Chronic Measles Infection of the Brain and Parkinsonism

H. Morita, S. Ikeda, M. Yazaki, 2000, European Neurology.

Coexistence of familial Mediterranean fever and Behçet's disease in a Japanese patient.

A. Nakamura, S. Ikeda, Takuhiro Yoshida, 2006, Internal medicine.

Comparison of the histological and immunohistochemical features of the thymus in young- and elderly-onset myasthenia gravis without thymoma

S. Ikeda, J. Nakayama, M. Matsuda, 2007, Journal of Clinical Neuroscience.

Retrospective analyses of clinical features and therapeutic outcomes in thymectomized patients with myasthenia gravis at Shinshu University.

A. Nakamura, H. Morita, T. Hashimoto, 2004, Internal medicine.

Lupus erythematosus profundus ( lupus panniculitis ) induced by interferon-β in a patient with multiple sclerosis

S. Ikeda, H. Murata, Y. Shimojima, 2007 .

Variability of beta-amyloid protein deposited lesions in Down's syndrome brains.

T. Tokuda, N. Yanagisawa, F. Kametani, 1994, The Tohoku journal of experimental medicine.

Bilirubin adsorption therapy and subsequent liver transplantation cured severe bilirubin encephalopathy in a long-term survival patient with Crigler-Najjar disease type I.

S. Ikeda, Y. Takei, H. Matsunami, 2000, Internal medicine.

[Diagnosis of familial amyloid polyneuropathy--gene analysis with primer-directed enzymatic amplification of DNA, isolation of plasma variant prealbumin and immunohistochemical identification of tissue amyloid protein].

Y. Sakaki, N. Yanagisawa, S. Ikeda, 1991, Rinshō shinkeigaku Clinical neurology.

Argentinian patients of European ancestry with familial amyloid polyneuropathy

N. Yanagisawa, S. Ikeda, Kanji Yamamoto, 1994 .

Electrophysiological features of familial amyloid polyneuropathy in endemic area

H. Morita, S. Ikeda, M. Kodaira, 2011, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

A pedigree analysis withminimised ascertainment biasshowsanticipation inMet3O-transthyre tin related familial amyloid polyneuropathy

S. Ikeda, 1998 .

Treatment of autonomic disorders in familial amyloid polyneuropathy with l-threo-3,4-dihydroxyphenilserine

N. Yanagisawa, S. Ikeda, N. Hanyu, 1987 .

Histochemical study of rectal aminergic nerves in type I familial amyloid polyneuropathy

Shigeaki Kobayashi, N. Yanagisawa, S. Ikeda, 1983, Neurology.

Identification of a novel transthyretin variant (Val30→Leu) associated with familial amyloidotic polyneuropathy

Kunihiro Yoshida, S. Ikeda, M. Nakazato, 1992, FEBS letters.

Transthyretin Met 30 familial amyloid polyneuropathy in China. Usefulness of mass spectrometry for screening a variant TTR in serum

A. Nakamura, T. Tokuda, N. Yanagisawa, 1997 .

Coexistence of familial transthyretin amyloidosis ATTR Val30Met and spinocerebellar ataxia type 1 in a Japanese family – A follow-up autopsy report

K. Arima, S. Ikeda, T. Oide, 2004, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

MRI analysis on a patient with the V30M mutation is characteristic of leptomeningeal amyloid

T. Tokuda, S. Ikeda, M. Yazaki, 2004, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Postmortem findings in two familial amyloidosis patients with transthyretin variant Asp38Ala

S. Ikeda, M. Yazaki, Y. Takei, 2000, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Diflunisal stabilizes familial amyloid polyneuropathy-associated transthyretin variant tetramers in serum against dissociation required for amyloidogenesis

Yoshiki Sekijima, Shu-ichi Ikeda, J. Kelly, 2006, Neuroscience Research.

Clinical Trial for Ttr Amyloidosis Using Diflunisal

R. Falk, M. Skinner, J. Kelly, 2007 .

Adult onset X-linked chronic granulomatous disease in a woman patient caused by a de novo mutation in paternal-origin CYBB gene and skewed inactivation of normal maternal X chromosome.

S. Ikeda, M. Yazaki, K. Agematsu, 2008, Internal medicine.

Multiple sclerosis with secondary syringomyelia An autopsy report

S. Ikeda, K. Tabata, M. Matsuda, 2001, Journal of the Neurological Sciences.

Abnormal conditioning effect of transcranial magnetic stimulation on soleus H-reflex during voluntary movement in Parkinson's disease

M. Shindo, H. Morita, T. Hashimoto, 2002, Clinical Neurophysiology.

Cancer-associated retinopathy in a patient with seminoma.

S. Ikeda, T. Kikuchi, D. Miyazaki, 2011, Retinal cases & brief reports.

Intestinal angina due to atherosclerosis in a 45-year-old systemic lupus erythematosus patient.

S. Ikeda, K. Sano, K. Tojo, 2010, Internal medicine.

The first pure form of Ostertag-type amyloidosis in Japan: a sporadic case of hereditary fibrinogen Aα-chain amyloidosis associated with a novel frameshift variant

F. Kametani, S. Nishio, S. Ikeda, 2015, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Advantage of administering tacrolimus for improving prognosis of patients with polymyositis and dermatomyositis

S. Ikeda, Y. Shimojima, Y. Sekijima, 2016, International journal of rheumatic diseases.

An Abnormal MRI Signal in Both Lateral Geniculate Bodies Is a Diagnostic Indicator for Patients with Behçet's Disease

S. Ikeda, M. Yazaki, M. Nakagawa, 2014, Case Reports in Neurology.

A primary Sjögren's syndrome patient with marked swelling of multiple exocrine glands and sclerosing pancreatitis.

S. Ikeda, S. Kawa, I. Nishimori, 2002, Internal medicine.

Clinical assessment of standing and gait in ataxic patients using a triaxial accelerometer

A. Nakamura, Kunihiro Yoshida, S. Ikeda, 2015, Cerebellum & Ataxias.

Effects of unilateral pallidotomy on voluntary movement, and simple and choice reaction times in Parkinson's disease

T. Hashimoto, R. Hayashi, S. Ikeda, 2003, Movement disorders : official journal of the Movement Disorder Society.

Long-term Trial of Corticosteroid Therapy for the Recurrence of Cerebral Amyloid Angiopathy-related Hemorrhages : A Case Study Using [11C] BF-227 Amyloid-PET

S. Ikeda, K. Machida, T. Yasude, 2014 .

Paradoxical modulation of tendon tap reflex during voluntary contraction in Parkinson's disease

M. Shindo, H. Morita, S. Ikeda, 2005, Clinical Neurophysiology.

Trientine increases fecal copper excretion in Wilson's disease: A case report

T. Tokuda, Kunihiro Yoshida, S. Ikeda, 2001 .

Unexpected Occurrence of Fetal Hemophagocytic Syndrome in a Patient with Hereditary Diffuse Leukoencephalopathy with Spheroids

Kunihiro Yoshida, S. Ikeda, T. Uehara, 2016 .

[Diagnostic significance of technetium-99m-pyrophosphate, technetium-99m-methylene diphosphonate and gallium-67-citrate scintigraphy in amyloid heart disease--a study with AL amyloidosis and familial amyloid polyneuropathy].

S. Ikeda, M. Hongo, H. Yamada, 1986, Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine.

Marked and rapid regression of hepatic amyloid deposition in a patient with systemic light chain (AL) amyloidosis after high-dose melphalan therapy with stem cell transplantation.

S. Ikeda, M. Matsuda, A. Matsushima, 2014, Internal medicine.

Distribution of neprilysin and deposit patterns of Aβ subtypes in the brains of aged squirrel monkeys (Saimiri sciureus)

S. Ikeda, Y. Une, J. Chambers, 2010, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

The diflunisal trial: update on study drug tolerance and disease progression

M. Skinner, P. Dyck, S. Ikeda, 2011, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

[Alzheimer's disease and amyloid beta-protein].

S. Ikeda, S Ikeda, 1989, No to shinkei = Brain and nerve.

Pallidotomy for severe generalized chorea of juvenile-onset dentatorubral-pallidoluysian atrophy

T. Hashimoto, S. Ikeda, T. Tada, 2003, Neurology.

No association between apolipoprotein E ϵ4 allele and the age of onset in type I familial amyloid polyneuropathy

T. Tokuda, N. Yanagisawa, F. Kametani, 1996, Neuroscience Letters.

An autopsy case with adult onset type II citrullinemia showing myelopathy

T. Saheki, S. Ikeda, Keiko Kobayashi, 2007, Journal of Neurological Sciences.

[Adult-onset citrullinemia].

S. Ikeda, 2007, No to shinkei = Brain and nerve.

[Adult-onset citrullinemia].

S. Ikeda, 2007, Brain and nerve = Shinkei kenkyu no shinpo.

First two cases of adult‐onset type II citrullinemia successfully treated by deceased‐donor liver transplantation in Japan

S. Ikeda, M. Yazaki, S. Miyagawa, 2012, Hepatology research : the official journal of the Japan Society of Hepatology.

Cessation of cerebral hemorrhage recurrence associated with corticosteroid treatment in a patient with cerebral amyloid angiopathy

A. Nakamura, Kunihiro Yoshida, S. Ikeda, 2000, Amyloid: Journal of Protein Folding Disorders.

Prednisolone (30–60 mg/day) for diseases other than AD decreases amyloid &bgr;-peptides in CSF

T. Tokuda, S. Ikeda, A. Tamaoka, 2002, Neurology.

Discriminative clinical and neuroimaging features of motor-predominant hereditary diffuse leukoencephalopathy with axonal spheroids and primary progressive multiple sclerosis: A preliminary cross-sectional study.

A. Hiwatashi, J. Kira, Kunihiro Yoshida, 2019, Multiple sclerosis and related disorders.

Clinical Management of AntiN-Methyl-D-Aspartate Receptor(NMDAR)Encephalitis Localization of NMDAR-related epitopes in ovarian teratoma : comparison between patients and controls

N. Tachibana, S. Ikeda, 2012 .

[Localization of NMDAR-related epitopes in ovarian teratoma: comparison between patients and controls].

N. Tachibana, S. Ikeda, 2012, Rinsho shinkeigaku = Clinical neurology.

A Long-Term Observation on the Possible Adverse Effects in Japanese Adolescent Girls after Human Papillomavirus Vaccination

S. Ikeda, A. Hineno, 2021, Vaccines.

A Case with XXXX Syndrome Who Was Incidentally Diagnosed during Examination for Suspected Post-Human Papillomavirus Vaccination Syndrome

S. Ikeda, H. Kato, Y. Sekijima, 2019, Case Reports in Clinical Medicine.

High prevalence of ATTR amyloidosis in endomyocardial biopsy-proven cardiac amyloidosis patients

S. Ikeda, K. Tojo, Y. Sekijima, 2013, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Pathological changes long after liver transplantation in a familial amyloidotic polyneuropathy patient

F. Kametani, H. Jono, S. Ikeda, 2012, BMJ Case Reports.

Relationship between clinical factors and neuropsychiatric manifestations in systemic lupus erythematosus

S. Ikeda, Y. Shimojima, M. Matsuda, 2005, Clinical Rheumatology.

A survey of epidemiology, clinical picture, and current treatments for elderly-onset (≥ 65) patients with myasthenia gravis in Nagano Prefecture, Japan

T. Hashimoto, S. Ikeda, M. Yazaki, 2017, Journal of the Neurological Sciences.

Disruption of blood–nerve barriers in hereditary transthyretin (ATTR) amyloidosis

G. Sobue, S. Ikeda, Y. Ando, 2017, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

[Identification of NMDA receptor in normal bovine ovary and ovum].

N. Tachibana, S. Ikeda, 2014, Rinsho shinkeigaku = Clinical neurology.

Decrease in presynaptic inhibition on heteronymous monosynaptic Ia terminals in patients with Parkinson's disease

M. Shindo, H. Morita, S. Ikeda, 2000, Movement disorders : official journal of the Movement Disorder Society.

Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy.

K. Arima, N. Ito, S. Ikeda, 2002, Neurology.

Impaired Left Ventricular Diastolic Properties in Patients with Familial Amyloid Polyneuropathy : A Study by Computerized M-Mode Echocardiography

S. Ikeda, M. Hongo, O. Kinoshita, 1988 .

Early Detection of Amyloid Heart Disease by Technetium-99M-Pyrophosphate Single-Photon Emission-Computed Tomography : A Study with Familial Amyloid Polyneuropathy

S. Ikeda, M. Hongo, O. Kinoshita, 1988 .

Amyloid β protein species in cerebrospinal fluid and in brain from patients with Down's syndrome

T. Tokuda, S. Ikeda, A. Tamaoka, 1999, Annals of neurology.

Primary AL amyloid polyneuropathy successfully treated with high‐dose melphalan followed by autologous stem cell transplantation

H. Morita, S. Ikeda, M. Yazaki, 2010, Muscle & nerve.

Bortezomib–dexamethasone versus high-dose melphalan for Japanese patients with systemic light-chain (AL) amyloidosis: a retrospective single-center study

S. Ikeda, Takuhiro Yoshida, Y. Shimojima, 2017, International Journal of Hematology.

Hypertrophic neuritis due to chronic inflammatory demyelinating polyradiculoneuropathy (CIDP): A postmortem pathological study

N. Yanagisawa, T. Inuzuka, S. Ikeda, 1996, Muscle & nerve.

Myasthenia gravis with anti-MuSK antibody, showing progressive muscular atrophy without blepharoptosis.

S. Ikeda, M. Yazaki, M. Motomura, 2005, Internal medicine.

Prevalence of Fabry disease and GLA c.196G>C variant in Japanese stroke patients

S. Ikeda, Katsuya Nakamura, M. Ota, 2017, Journal of Human Genetics.

p.E66Q mutation in the GLA gene is associated with a high risk of cerebral small‐vessel occlusion in elderly Japanese males

Y. Fukushima, F. Endo, S. Ikeda, 2014, European journal of neurology.

Transthyretin Val30Met familial amyloid polyneuropathy: a considerably different clinical picture and natural course in endemic and non-endemic areas

S. Ikeda, 2012, Journal of Neurology Neurosurgery & Psychiatry.

Characteristic spinal MRI findings of HIV-associated myelopathy in an AIDS patient.

H. Morita, T. Hashimoto, S. Ikeda, 2005, Internal medicine.

Successful Pharmacotherapy for an Adult Case with Prolonged Symptoms of Postganglionic Cholinergic Dysautonomia

S. Ikeda, T. Oide, Kanji Yamamoto, 2004, European Neurology.

Cardiac amyloid in patients with familial amyloid polyneuropathy consists of abundant wild-type transthyretin.

T. Tokuda, J. Koyama, F. Kametani, 2000, Biochemical and biophysical research communications.

A study of the morphology and distribution of amyloid beta protein immunoreactive plaque and related lesions in the brains of Alzheimer's disease and adult Down's syndrome.

G. Glenner, D. Allsop, S. Ikeda, 1989, Progress in clinical and biological research.

A study of the morphology and distribution of amyloid β protein immunoreactive plaque and related lesions in the brains of Alzheimer's disease and adult Down's syndrome

G. Glenner, D. Allsop, S. Ikeda, 1989 .

Migrating osteoarthralgia: a rare initial manifestation of adult leukemia.

S. Ikeda, Toshiro Ito, M. Matsuda, 2006, Internal medicine.

An Adolescent Case of Citrin Deficiency With Severe Anorexia Mimicking Anorexia Nervosa

A. Inui, S. Ikeda, M. Yazaki, 2015, Pediatrics.

[Therapeutic approaches for patients with adult-onset type II citrullinemia (CTLN2): effectiveness of treatment with low-carbohydrate diet and sodium pyruvate].

T. Saheki, S. Ikeda, Keiko Kobayashi, 2010, Rinsho shinkeigaku = Clinical neurology.

SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein.

I. Kanazawa, S. Tsuji, Koichiro Nakamura, 2001, Human molecular genetics.

Multiple mitochondrial DNA deletions in a patient with mitochondrial myopathy and cardiomyopathy but no ophthalmoplegia

N. Yanagisawa, S. Ikeda, Y. Takei, 1995, Muscle & nerve.

Pathology of early- vs late-onset TTR Met30 familial amyloid polyneuropathy

G. Sobue, N. Hattori, S. Ikeda, 2004, Neurology.

Senile systemic amyloidosis presenting as bilateral carpal tunnel syndrome

T. Tokuda, S. Saitoh, S. Ikeda, 2002, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Progressive Wild‐Type Transthyretin Deposition after Liver Transplantation Preferentially Occurs onto Myocardium in FAP Patients

T. Tokuda, J. Koyama, F. Kametani, 2007, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

Late-onset familial amyloid polyneuropathy type I (transthyretin Met30-associated familial amyloid polyneuropathy) unrelated to endemic focus in Japan. Clinicopathological and genetic features.

G. Sobue, N. Hattori, S. Ikeda, 1999, Brain : a journal of neurology.

Effect of synovial transthyretin amyloid deposition on preoperative symptoms and postoperative recovery of median nerve function among patients with idiopathic carpal tunnel syndrome

T. Imaeda, S. Ikeda, T. Moriizumi, 2014, Journal of orthopaedic science : official journal of the Japanese Orthopaedic Association.

Senile systemic amyloidosis: clinical pictures and diagnostic criteria

S. Ikeda, 2011, Amyloid: Journal of Protein Folding Disorders.

Significant deposition of wild type transthyretin-derived amyloid in the gastrointestinal tract of aged individuals

T. Hashimoto, S. Ikeda, K. Tojo, 2009, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Age associated axonal features in HNPP with 17p11.2 deletion in Japan

G. Sobue, N. Hattori, K. Nakashima, 2005, Journal of Neurology, Neurosurgery & Psychiatry.

[A 36-year-old woman with primary central nervous system lymphoma diagnosed by twice brain biopsies, showing relapsing and remitting brain lesions].

S. Ikeda, C. Kobayashi, Tomoki Kaneko, 2018, Rinsho shinkeigaku = Clinical neurology.

A Physician's Guide to Transthyretin Amyloidosis

R. Falk, M. Maurer, S. Ikeda, 2008 .

Thalamic Stimulation for Disabling Tremor in a Patient with Spinocerebellar Degeneration

K. Hongo, T. Hashimoto, T. Goto, 2005, Stereotactic and Functional Neurosurgery.

Amyloid beta protein and its 3-kDa fragment are present in the axoplasm fraction of the white matter in human brain.

T. Tokuda, K. Tanaka, N. Yanagisawa, 1996, Biochemical and Biophysical Research Communications - BBRC.

Non-herpetic fulminant meningoencephalitis with periodic lateralised epileptiform discharges

A. Nakamura, T. Hashimoto, N. Yanagisawa, 2002, Journal of Clinical Neuroscience.

Editorial Amyloid fibril protein

C. Masters, S. Ikeda, G. Merlini, 2002 .

Inadequate Modulation of Excitability With Voluntary Dorsiflexion in Parkinson's Disease

H. Morita, S. Ikeda, M. Kodaira, 2014, Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society.

Principal component analysis for ataxic gait using a triaxial accelerometer

Kunihiro Yoshida, S. Ikeda, H. Genno, 2017, Journal of NeuroEngineering and Rehabilitation.

Exome sequencing reveals a homozygous SYT14 mutation in adult-onset, autosomal-recessive spinocerebellar ataxia with psychomotor retardation.

H. Morita, Y. Kuroiwa, S. Tsuji, 2011, American journal of human genetics.

Reversible extensive leukoencephalopathy in Sweet disease: A case report

H. Morita, Kunihiro Yoshida, S. Ikeda, 2008, Journal of the Neurological Sciences.

Steatogenesis in adult-onset type II citrullinemia is associated with down-regulation of PPARα.

F. Gonzalez, S. Ikeda, T. Aoyama, 2015, Biochimica et biophysica acta.

The Diflunisal Trial: Study accrual and drug tolerance

M. Skinner, P. Dyck, S. Ikeda, 2012, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

The safety of transcranial magnetic stimulation with deep brain stimulation instruments.

H. Morita, T. Hashimoto, S. Ikeda, 2010, Parkinsonism & Related Disorders.

The safety of transcranial magnetic stimulation with deep brain stimulation instruments.

H. Morita, T. Hashimoto, S. Ikeda, 2010, Parkinsonism & Related Disorders.

Progressive supranuclear palsy‐like syndrome in two siblings of a consanguineous marriage

H. Morita, N. Yanagisawa, S. Ohara, 1992, Neurology.

Squatting-induced bilateral peroneal nerve palsy in a sewer pipe worker.

S. Ikeda, M. Kodaira, N. Ohashi, 2017, Occupational medicine.

A Japanese case of SCA14 with the Gly128Asp mutation

H. Morita, Kunihiro Yoshida, S. Ikeda, 2006, Journal of Human Genetics.

Liver Transplantation Is a Potential Treatment Option for Systemic Light Chain Amyloidosis Patients with Dominant Hepatic Involvement: A Case Report and Analytical Review of the Literature.

M. Makuuchi, S. Ikeda, A. Ueno, 2016, Internal medicine.