I. Yabe

发表

Mutations in COQ2 in familial and sporadic multiple-system atrophy.

J. Trojanowski, S. Gilman, K. Shirahige, 2013, The New England journal of medicine.

Safety and efficacy of eculizumab in Guillain-Barré syndrome: a multicentre, double-blind, randomised phase 2 trial

G. Sobue, K. Hirata, K. Kaida, 2018, The Lancet Neurology.

3D neuromelanin-sensitive magnetic resonance imaging with semi-automated volume measurement of the substantia nigra pars compacta for diagnosis of Parkinson’s disease

Hiroki Shirato, Satoshi Terae, Kohsuke Kudo, 2013, Neuroradiology.

Progressive anterior operculum syndrome due to FTLD-TDP: a clinico-pathological investigation

M. Otsuki, K. Wakabayashi, F. Mori, 2010, Journal of Neurology.

Vocal cord abductor paralysis in spinocerebellar ataxia type 1

H. Mizusawa, K. Tashiro, T. Tsunemi, 1999, Journal of neurology, neurosurgery, and psychiatry.

Plasma matrix metalloproteinase‐3 correlates with the clinical severity in men with multiple system atrophy

A. Kakita, Hitoshi Takahashi, K. Wakabayashi, 2013 .

The Responsiveness of Triaxial Accelerometer Measurement of Gait Ataxia Is Higher than That of the Scale for the Assessment and Rating of Ataxia in the Early Stages of Spinocerebellar Degeneration

K. Takakusaki, H. Sasaki, I. Yabe, 2019, The Cerebellum.

Estimation of skeletal muscle energy metabolism in Machado‐Joseph disease using 31P‐MR spectroscopy

S. Terae, H. Sasaki, K. Tha, 2011, Movement disorders : official journal of the Movement Disorder Society.

Mapping of autosomal dominant cerebellar ataxia without the pathogenic PPP2R2B mutation to the locus for spinocerebellar ataxia 12.

S. Tsuji, Y. Fukuda, H. Sasaki, 2010, Archives of neurology.

[Idiopathic intracranial hypertension without headache detected during a routine health check].

H. Sasaki, I. Yabe, S. Tsuji, 2008, Rinsho shinkeigaku = Clinical neurology.

Associations between multiple system atrophy and polymorphisms of SLC1A4, SQSTM1, and EIF4EBP1 Genes

H. Sasaki, H. Soma, I. Yabe, 2008, Movement disorders : official journal of the Movement Disorder Society.

Proteasome inhibition induces selective motor neuron death in organotypic slice cultures

S. Yamagishi, M. Takeuchi, S. Kikuchi, 2005, Journal of neuroscience research.

GNE mutations causing distal myopathy with rimmed vacuoles with inflammation

S. Kikuchi, K. Tashiro, H. Sasaki, 2003, Neurology.

Inappropriate Metacognitive Status Increases State Anxiety in Genetic Counseling Clients

I. Yabe, M. Matsushima, M. Takeuchi, 2022, Frontiers in Psychology.

A diagnostic index based on quantitative susceptibility mapping and voxel-based morphometry may improve early diagnosis of Alzheimer’s disease

M. Sasaki, K. Kudo, Tomoki Amemiya, 2022, European Radiology.

Microstructural white matter abnormalities of multiple system atrophy: in vivo topographic illustration by using diffusion-tensor MR imaging.

H. Shirato, S. Terae, K. Kudo, 2010, Radiology.

Moyamoya Disease Associated with a Deficiency of Complement Component 6.

M. Fujimura, T. Atsumi, T. Sugiyama, 2022, Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.

Spinocerebellar ataxia type 14 caused by a mutation in protein kinase C gamma.

S. Tsuji, T. Bird, S. Kikuchi, 2003, Archives of neurology.

Brefeldin A‐induced neurotoxicity in cultured spinal cord neurons

S. Kikuchi, K. Tashiro, K. Shinpo, 2003, Journal of neuroscience research.

Effect of proteasome inhibitor on cultured mesencephalic dopaminergic neurons

Z. Makita, S. Yamagishi, M. Takeuchi, 2003, Brain Research.

A Retrospective Epidemiological Study of Tick-Borne Encephalitis Virus in Patients with Neurological Disorders in Hokkaido, Japan

K. Yoshii, H. Sasaki, I. Yabe, 2020, Microorganisms.

MRI and pathological findings of rheumatoid meningitis

H. Sasaki, H. Yaguchi, I. Yabe, 2010, Journal of Clinical Neuroscience.

The disease sites of female genital cancers of BRCA1/2-associated hereditary breast and ovarian cancer: a retrospective study

H. Watari, M. Sekine, T. Enomoto, 2021, World Journal of Surgical Oncology.

Effect of geranylgeranylaceton on cellular damage induced by proteasome inhibition in cultured spinal neurons

M. Takeuchi, S. Kikuchi, K. Tashiro, 2002, Journal of neuroscience research.

Predisposing chromosome for spinocerebellar ataxia type 6 (SCA6) in Japanese

M. Nishizawa, Y. Takiyama, K. Tashiro, 2001, Journal of medical genetics.

Risk factors for lymph node metastasis of ovarian, fallopian tube and primary peritoneal cancer in hereditary breast and ovarian cancer syndrome.

H. Watari, M. Sekine, T. Enomoto, 2020, Japanese journal of clinical oncology.

Variants associated with Gaucher disease in multiple system atrophy

J. Trojanowski, S. Gilman, Y. Kuroiwa, 2015, Annals of clinical and translational neurology.

No association between FMR1 premutations and multiple system atrophy

H. Sasaki, H. Soma, I. Yabe, 2004, Journal of Neurology.

Nationwide survey on the epidemiology of syringomyelia in Japan

S. Terae, R. Uehara, I. Nakano, 2012, Journal of the Neurological Sciences.

Brain SPECT analysis by 3D-SSP and clinical features of Parkinson's disease.

S. Kikuchi, K. Tashiro, H. Sasaki, 2006, [Hokkaido igaku zasshi] The Hokkaido journal of medical science.

Twenty CAG repeats are sufficient to cause the SCA6 phenotype

S. Kikuchi, K. Tashiro, H. Sasaki, 2001, Journal of medical genetics.

Isolated granulomatous angiitis with eosinophilia in the central nervous system

H. Sasaki, T. Kano, I. Yabe, 2013 .

Quantitative evaluation of gait ataxia by accelerometers

Mitsuru Yoneyama, M. Yoneyama, H. Sasaki, 2015, Journal of the Neurological Sciences.

[Reliability of the Japanese version of the Scale for the Assessment and Rating of Ataxia (SARA)].

G. Sobue, K. Nakashima, T. Shimohata, 2009, Brain and nerve = Shinkei kenkyu no shinpo.

Clinical characterization and successful treatment of 6 patients with Churg–Strauss syndrome-associated neuropathy

H. Sasaki, H. Yaguchi, I. Yabe, 2009, Clinical neurology and neurosurgery (Dutch-Flemish ed. Print).

Cystatin C in cerebrospinal fluid as a biomarker of ALS

S. Kikuchi, H. Sasaki, I. Yabe, 2009, Neuroscience Letters.

Open-label 24-week extension study of edaravone (MCI-186) in amyotrophic lateral sclerosis

H. Sasaki, I. Yabe, M. Fukuchi, 2017, Amyotrophic lateral sclerosis & frontotemporal degeneration.

MSA-C is the predominant clinical phenotype of MSA in Japan: Analysis of 142 patients with probable MSA

H. Sasaki, H. Soma, I. Yabe, 2006, Journal of the Neurological Sciences.

Urinary dysfunction and motor symptoms in untreated Parkinson's disease

H. Yaguchi, I. Yabe, Y. Tajima, 2016, Journal of the Neurological Sciences.

Effects of age and glucose levels on lactate levels in cerebrospinal fluid examination of neurodegenerative diseases

H. Sasaki, I. Yabe, K. Sakushima, 2017, Journal of the Neurological Sciences.

Instructions for use Title Heredity in Multiple System Atrophy

H. Sasaki, H. Soma, I. Yabe, 2016 .

Short communication Heredity in multiple system atrophy

H. Sasaki, H. Soma, I. Yabe, 2006 .

MM2 cortical form of sporadic Creutzfeldt-Jakob disease without progressive dementia and akinetic mutism: A case deviating from current diagnostic criteria

K. Eguchi, H. Sasaki, K. Satoh, 2020, Journal of the Neurological Sciences.

Genetic analysis of two Japanese families with progressive external ophthalmoplegia and parkinsonism

S. Saitoh, H. Sasaki, H. Yaguchi, 2011, Journal of Neurology.

Mutations in bassoon in individuals with familial and sporadic progressive supranuclear palsy-like syndrome

M. Hasegawa, S. Hatakeyama, K. Wakabayashi, 2017, Scientific Reports.

Randomized phase 2 study of perampanel for sporadic amyotrophic lateral sclerosis

G. Sobue, T. Kanda, K. Abe, 2021, Journal of Neurology.

Clinical, pathological, and genetic mutation analysis of sporadic inclusion body myositis in Japanese people

H. Sasaki, T. Kano, I. Yabe, 2012, Journal of Neurology.

Meta-iodobenzylguanidine myocardial scintigraphy in Perry disease.

N. Hattori, K. Shiomi, Y. Tsuboi, 2021, Parkinsonism & related disorders.

[Gliomatosis cerebri with multifocal progressive lesions on MRI].

Y. Sawamura, H. Sasaki, I. Yabe, 2011, Rinsho shinkeigaku = Clinical neurology.

A Prospective, Multicenter, Randomized Phase II Study to Evaluate the Efficacy and Safety of Eculizumab in Patients with Guillain-Barré Syndrome (GBS): Protocol of Japanese Eculizumab Trial for GBS (JET-GBS)

S. Tsuji, K. Hirata, J. Kira, 2016, JMIR research protocols.

Association of Smoking and Generalized Manifestations of Myasthenia Gravis

I. Yabe, K. Sakushima, M. Niino, 2021, Internal medicine.

A patient with spastic paralysis finally diagnosed as V180I genetic Creutzfeldt-Jakob disease 9 years after onset

K. Satoh, T. Kitamoto, I. Yabe, 2020, Prion.

Genetic interaction of hnRNPA2B1 and DNAJB6 in a Drosophila model of multisystem proteinopathy.

Brian D. Freibaum, A. Kanagaraj, J. Taylor, 2016, Human molecular genetics.

Amyotrophic lateral sclerosis with frontotemporal dementia (ALS-FTD) syndrome as a phenotype of Creutzfeldt-Jakob disease (CJD)? A case report

F. Moriwaka, H. Sasaki, K. Satoh, 2017, Journal of the Neurological Sciences.

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.

Improved Long-Term Survival with Edaravone Therapy in Patients with Amyotrophic Lateral Sclerosis: A Retrospective Single-Center Study in Japan

A. Nagai, T. Kano, I. Yabe, 2021, Pharmaceuticals.

Spastin gene mutation in Japanese with hereditary spastic paraplegia

K. Tashiro, H. Sasaki, H. Sasaki, 2002, Journal of medical genetics.

Clinical features of spinal cord sarcoidosis : analysis of 17 neurosarcoidosis patients

H. Sasaki, I. Yabe, K. Sakushima, 2018 .

Sez6l2 regulates phosphorylation of ADD and neuritogenesis.

Masahiko Watanabe, K. Nakayama, M. Matsumoto, 2017, Biochemical and biophysical research communications.

Identification of anti-Sez6l2 antibody in a patient with cerebellar ataxia and retinopathy

K. Nakayama, M. Matsumoto, S. Hatakeyama, 2013, Journal of Neurology.

Novel GNE compound heterozygous mutations in a GNE myopathy patient

H. Sasaki, T. Kano, I. Yabe, 2013, Muscle & nerve.

[Case of toxoplasma encephalopathy with specific MRI findings, diagnosed by IgG avidity index and nested PCR].

H. Sasaki, I. Yabe, Y. Tajima, 2010, Rinsho shinkeigaku = Clinical neurology.

A Japanese case of steroid responsive myopathy with deficient chondroitin sulphate

S. Kikuchi, K. Tashiro, I. Yabe, 2002, Journal of neurology, neurosurgery, and psychiatry.

Successful treatment of cerebral embolism in a juvenilewoman using intravenous rt-PA

H. Sasaki, I. Yabe, Y. Mito, 2011 .

Clinical features of anti-mitochondrial M2 antibody-positive myositis: case series of 17 patients

A. Nagai, T. Nagai, T. Anzai, 2022, Journal of the Neurological Sciences.

Pathological study of subacute autoimmune encephalopathy with anti-AQP4 antibodies in a pregnant woman

K. Fujihara, T. Misu, H. Sasaki, 2012, Multiple Sclerosis.

Incidence of idiopathic intracranial hypertension in Hokkaido, the northern-most island in Japan

K. Tashiro, F. Moriwaka, I. Yabe, 2000, Journal of Neurology.

Familial syringomyelia: the first Japanese case and review of the literature

S. Kikuchi, K. Tashiro, I. Yabe, 2002, Clinical Neurology and Neurosurgery.

Multiphasic demyelinating disorder with acute transverse myelitis in Japanese

S. Kikuchi, K. Tashiro, I. Yabe, 2003, Journal of Neurology.

Multiphasic demyelinat- ing disorder with acute transverse myelitis

S. Kikuchi, K. Tashiro, I. Yabe, 2003 .

Vitamin D receptor gene polymorphism in multiple sclerosis and the association with HLA class II alleles

S. Kikuchi, K. Tashiro, H. Sasaki, 2000, Journal of the Neurological Sciences.

X-linked Charcot-Marie-Tooth disease (CMTX) in a severely affected female patient with scattered lesions in cerebral white matter.

H. Sasaki, H. Soma, I. Yabe, 2007, Internal medicine.

Neurovascular changes in magnetic resonance imagining and single-photon emission computed tomography during migraine attack in patients with FHM2 mutations

A. Nagai, Yuji Takahashi, I. Yabe, 2020 .

[A case of Guillain-Barré syndrome following hepatitis E virus infection].

I. Yabe, M. Matsushima, R. Ando, 2021, Rinsho shinkeigaku = Clinical neurology.

[Initial symptoms and mode of neurological progression in spinocerebellar ataxia type 6 (SCA6)].

K. Tashiro, H. Sasaki, I. Yabe, 1998, Rinsho shinkeigaku = Clinical neurology.

Instructions for use Title Dissociation between the severity of cerebrospinal fluid hypovolemia and MRI findings

H. Sasaki, I. Yabe, K. Sakushima, 2017 .

Dissociation between the severity of cerebrospinal fluid hypovolemia and MRI findings

H. Sasaki, I. Yabe, K. Sakushima, 2010, Journal of Neurology.

Reversible splenial lesion in new-onset refractory status epilepticus: A case report

H. Sasaki, I. Yabe, Katsuki Eguchi, 2019, Clinical Neurology and Neurosurgery.

Association of vitamin D receptor gene polymorphism with multiple sclerosis in Japanese

K. Miyasaka, S. Kikuchi, K. Tashiro, 1999, Journal of the Neurological Sciences.

Establishing diagnostic criteria for Perry syndrome

M. Farrer, D. Dickson, R. Neshige, 2017, Journal of Neurology, Neurosurgery, and Psychiatry.

Amyloid Polyneuropathy and Myocardial Amyloidosis 10 Years after Domino Liver Transplantation from a Patient with a Transthyretin Ser50Arg Mutation

H. Sasaki, T. Shimamura, I. Yabe, 2017, Internal medicine.

[Successful cyclosporine treatment in 2 patients with refractory CIDP, involving monitoring of both AUC(0-4h) and trough levels].

H. Sasaki, T. Kano, I. Yabe, 2012, Rinsho shinkeigaku = Clinical neurology.

Chronic Inflammatory Demyelinating Polyneuropathy after Treatment with Interferon-α

H. Sasaki, I. Yabe, M. Hirotani, 2009 .

Chronic deep brain stimulation reduces cortical β-γ phase amplitude-coupling in patients with Parkinson's disease.

K. Houkin, H. Shiraishi, M. Kitagawa, 2021, Parkinsonism & related disorders.

Frontotemporal dementia and progressive supranuclear palsy‐like syndrome with a novel TARDBP mutation

H. Sasaki, I. Yabe, I. Takahashi, 2016 .

Transient subacute cerebellar ataxia in a patient with Lambert-Eaton myasthenic syndrome after intracranial aneurysm surgery

M. Motomura, H. Sasaki, H. Yaguchi, 2008, Clinical Neurology and Neurosurgery.

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.

Idiopathic Hypoglossal Nerve Laceration Detected by High‐Resolution Three‐Dimensional Constructive Interference in Steady State Magnetic Resonance Imaging

S. Terae, H. Sasaki, I. Yabe, 2011, Journal of neuroimaging : official journal of the American Society of Neuroimaging.

[Treatment of intractable tuberculous meningitis using intrathecal isoniazid administration and steroid pulse therapy; a report of two cases].

H. Sasaki, T. Kano, I. Yabe, 2012, Rinsho shinkeigaku = Clinical neurology.

Cat Scratch Disease-associated Encephalitis Followed by Parkinsonism

H. Soma, I. Yabe, S. Ura, 2022, Internal medicine.

Novel mutation in the ALPL gene with a dominant negative effect in a Japanese family

Y. Kitagawa, Kanako Tachikawa, T. Michigami, 2021, Journal of Bone and Mineral Metabolism.

DNAJB6 myopathy in an Asian cohort and cytoplasmic/nuclear inclusions

I. Nonaka, Y. Hayashi, I. Nishino, 2013, Neuromuscular Disorders.

Safety and efficacy of edaravone in well defined patients with amyotrophic lateral sclerosis: a randomised, double-blind, placebo-controlled trial

Y. Itoyama, S. Tsuji, G. Sobue, 2017, The Lancet Neurology.

HLA-DPB1*0501 is not uniquely associated with opticospinal multiple sclerosis in Japanese patients. Important role of DPB1*0301

S. Kikuchi, H. Sasaki, I. Yabe, 2006, Multiple sclerosis.

HLA-related subpopulations of MS in Japanese with and without oligoclonal IgG bands

S. Kikuchi, K. Tashiro, S. Hashimoto, 2003, Neurology.

Mutation screening of the DNAJC7 gene in Japanese patients with sporadic amyotrophic lateral sclerosis

G. Sobue, N. Hattori, K. Nakashima, 2021, Neurobiology of Aging.

Spectrum and prevalence of autosomal dominant spinocerebellar ataxia in Hokkaido, the northern island of Japan: a study of 113 Japanese families

H. Sasaki, H. Soma, I. Yabe, 2007, Journal of Human Genetics.

The hereditary spinocerebellar ataxias in Japan

K. Tashiro, H. Sasaki, H. Sasaki, 2003, Cytogenetic and Genome Research.

Genomic copy number variation analysis in multiple system atrophy

Ichigaku Takigawa, H. Sasaki, Takayuki Katayama, 2017, Molecular Brain.

[A case of Emery-Dreifuss muscular dystrophy with slight joint contracture].

Yoshihiko Saito, I. Nishino, I. Yabe, 2020, Rinsho shinkeigaku = Clinical neurology.

Hodgkin's disease irradiated with the inverted-Y technique.

T. Landberg, I. Yabe, C. Mercke, 1981, Acta radiologica. Oncology.

Neuromyelitis Optica Spectrum Disorder with Recurrent Intracranial Hemorrhage

H. Yaguchi, I. Yabe, Y. Tajima, 2017, Internal medicine.

Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy Presenting with Area Postrema Syndrome-Like Symptoms without Medulla Oblongata Lesions

T. Shimohata, I. Yabe, A. Kimura, 2022, Neuroimmunomodulation.

Clinical significance of comprehensive genomic profiling tests covered by public insurance in patients with advanced solid cancers in Hokkaido, Japan.

Y. Matsuno, Masato Takahashi, H. Dosaka-akita, 2021, Japanese journal of clinical oncology.

TNF-related apoptosis inducing ligand (TRAIL) gene polymorphism in Japanese patients with multiple sclerosis

S. Kikuchi, H. Sasaki, I. Yabe, 2005, Journal of Neuroimmunology.

Secretion of DJ-1 into the serum of patients with Parkinson's disease

H. Ariga, H. Sasaki, I. Yabe, 2008, Neuroscience Letters.

Clinical impact of a cancer genomic profiling test using an in‐house comprehensive targeted sequencing system

H. Dosaka-akita, I. Kinoshita, I. Yabe, 2020, Cancer science.

[Reliability of blood gas analyzers for measuring lactate levels in cerebrospinal fluid].

H. Sasaki, I. Yabe, K. Sakushima, 2009, Rinsho shinkeigaku = Clinical neurology.

Clinical efficacy of istradefylline on lower urinary tract symptoms in Parkinson's disease

N. Shinohara, H. Sasaki, I. Yabe, 2016, International journal of urology : official journal of the Japanese Urological Association.

Aseptic meningitis with relapsing polychondritis mimicking bacterial meningitis.

H. Sasaki, H. Yaguchi, I. Yabe, 2009, Internal medicine.

MERRF/MELAS overlap syndrome: a double pathogenic mutation in mitochondrial tRNA genes

S. Saitoh, H. Sasaki, H. Yaguchi, 2010, Journal of Medical Genetics.

Caveolin‐3 gene mutation in Japanese with rippling muscle disease

S. Kikuchi, K. Tashiro, H. Sasaki, 2003, Acta neurologica Scandinavica.

[A case of Lyme neuroborreliosis without erythema migrans].

H. Sasaki, I. Yabe, Katsuki Eguchi, 2018, Rinsho shinkeigaku = Clinical neurology.

[Familial progressive external opthalmoplegia, parkinsonism and polyneuropathy associated with POLG1 mutation].

I. Nakano, H. Sasaki, I. Yabe, 2014, Rinsho shinkeigaku = Clinical neurology.

Positional vertigo and macroscopic downbeat positioning nystagmus in spinocerebellar ataxia type 6 (SCA6)

K. Fukushima, K. Tashiro, H. Sasaki, 2003, Journal of Neurology.

No association of vitamin D-binding protein gene polymorphisms in Japanese patients with MS

S. Kikuchi, K. Tashiro, I. Yabe, 2002, Journal of Neuroimmunology.

Incidence of anti-NMDAR encephalitis in patients undergoing resection of ovarian teratoma in a single institution

H. Yaguchi, I. Yabe, Keiko Tanaka, 2019, Journal of the Neurological Sciences.

Heat shock protein 70 gene polymorphism in Japanese patients with multiple sclerosis.

S. Kikuchi, K. Tashiro, H. Sasaki, 2001, Tissue antigens.

SCA42 mutation analysis in a case series of Japanese patients with spinocerebellar ataxia

S. Tsuji, H. Sasaki, I. Yabe, 2017, Journal of Human Genetics.

Symptomatic narcolepsy in patients with neuromyelitis optica and multiple sclerosis: new neurochemical and immunological implications.

T. Shimohata, S. Nishino, M. Nishizawa, 2009, Archives of neurology.

CTLA-4 gene polymorphism may modulate disease in Japanese multiple sclerosis patients

K. Miyasaka, S. Kikuchi, K. Tashiro, 1999, Journal of the Neurological Sciences.

Rare frequency of downbeat positioning nystagmus in spinocerebellar ataxia type 31

Kunihiro Yoshida, H. Sasaki, I. Yabe, 2015, Journal of the Neurological Sciences.

Estrogen receptor gene polymorphism in Japanese patients with multiple sclerosis

S. Kikuchi, K. Tashiro, I. Yabe, 2000, Journal of the Neurological Sciences.

Impact of clinical targeted sequencing on endocrine responsiveness in estrogen receptor-positive, HER2-negative metastatic breast cancer

H. Yamashita, I. Kinoshita, I. Yabe, 2021, Scientific Reports.

Prevalence of triplet repeat expansion in ataxia patients from Hokkaido, the northernmost island of Japan

K. Tashiro, H. Sasaki, I. Yabe, 2000, Journal of the Neurological Sciences.

Genetic polymorphisms of IL-1β and IL-1 receptor antagonist in association with multiple sclerosis in Japanese patients

S. Kikuchi, K. Tashiro, H. Sasaki, 2001, Journal of Neuroimmunology.

Constant current stimulation may improve apraxia of eyelid opening induced by deep brain stimulation

K. Houkin, H. Sasaki, T. Seki, 2020 .

[A case of primary diffuse leptomeningeal gliomatosis, clinically indistinguishable from metastatic meningeal carcinomatosis].

A. Ishizu, H. Sasaki, I. Yabe, 2011, Rinsho shinkeigaku = Clinical neurology.

Decreased IL-10 production mediated by Toll-like receptor 9 in B cells in multiple sclerosis

S. Kikuchi, H. Sasaki, I. Yabe, 2010, Journal of Neuroimmunology.

Reply to: The Letter to be published with the Letter, Amyotrophic lateral sclerosis with frontotemporal dementia (ALS-FTD) syndrome as a phenotype of Creutzfeldt-Jakob disease (CJD)? A case report

F. Moriwaka, H. Sasaki, K. Satoh, 2017, Journal of the Neurological Sciences.

Level of plasma neuregulin-1 SMDF is reduced in patients with idiopathic Parkinson’s disease

K. Wakabayashi, H. Sasaki, T. Kano, 2015, Neuroscience Letters.

The clinical and genetic spectrum of spinocerebellar ataxia 14

H. Zoghbi, T. Bird, R. Margolis, 2005, Neurology.

Spinocerebellar ataxia type 14 caused by a mutation in protein kinase C gamma.

S. Tsuji, T. Bird, S. Kikuchi, 2003, Archives of neurology.

A novel locus for dominant cerebellar ataxia (SCA14) maps to a 10.2‐cM interval flanked by D19S206 and D19S605 on chromosome 19q13.4‐qter

S. Tsuji, M. Nishizawa, Y. Takiyama, 2000, Annals of neurology.

A 3-year cohort study of the natural history of spinocerebellar ataxia type 6 in Japan

S. Tsuji, G. Sobue, K. Nakashima, 2014, Orphanet Journal of Rare Diseases.

An examination of the Apo-1/Fas promoter Mva I polymorphism in Japanese patients with multiple sclerosis

S. Kikuchi, K. Tashiro, I. Yabe, 2002, BMC neurology.

Extramedullary plasmacytoma involving perirenal space accompanied by extramedullary hematopoiesis and amyloid deposition

H. Shirato, Ardene A. Harris, S. Terae, 2010, Japanese Journal of Radiology.

Number of surgeries performed during the lifetime of patients with myelomeningocele.

M. Nonaka, I. Yabe, A. Asai, 2022, Journal of neurosurgery. Pediatrics.

Anti-Sez6l2 antibody detected in a patient with immune-mediated cerebellar ataxia inhibits complex formation of GluR1 and Sez6l2

Masahiko Watanabe, S. Hatakeyama, H. Yaguchi, 2018, Journal of Neurology.

Polymorphisms of apolipoprotein E and Japanese patients with multiple sclerosis

S. Kikuchi, K. Tashiro, I. Yabe, 2003, Multiple sclerosis.

Four mutations of the spastin gene in Japanese families with spastic paraplegia

H. Tachibana, H. Sasaki, S. Kuzuhara, 2006, Journal of Human Genetics.

An examination of the association between b2 adrenergic receptor polymorphisms and multiple sclerosis

S. Kikuchi, K. Tashiro, I. Yabe, 2002, Multiple sclerosis.

Progressive multifocal leukoencephalopathy with mild clinical conditions and detection of archetype-like JC virus in cerebrospinal fluid

M. Yamada, A. Nagai, I. Yabe, 2021, Journal of NeuroVirology.

Identification of plasma microRNAs as a biomarker of sporadic Amyotrophic Lateral Sclerosis

H. Sasaki, T. Kano, I. Yabe, 2015, Molecular Brain.

Effects of Extracranial–Intracranial Bypass for Patients With Hemorrhagic Moyamoya Disease: Results of the Japan Adult Moyamoya Trial

S. Kuroda, H. Nakase, H. Fukuyama, 2014, Stroke.

Entacapone, a catechol-O-methyltransferase inhibitor, improves the motor activity and dopamine content of basal ganglia in a rat model of Parkinson's disease induced by Japanese encephalitis virus

M. Hirafuji, Shirou Tsuchida, N. Hamaue, 2010, Brain Research.

[Case of intravascular lymphoma with a longitudinal spinal lesion diagnosed by multiple biopsies].

S. Murayama, H. Sasaki, I. Yabe, 2012, Rinsho shinkeigaku = Clinical neurology.

Neuromelanin MRI in a family with mitochondrial parkinsonism harboring a Y955C mutation in POLG1.

H. Sasaki, I. Yabe, Yu-ichi Goto, 2013, Parkinsonism & related disorders.

Treatment of cerebellar ataxia with 5-HT1A agonist

H. Sasaki, I. Yabe, A. Takei, 2008, The Cerebellum.

Effects of Tandospirone on “5-HT1A Receptor-Associated Symptoms” in Patients with Machado-Josephe Disease: An Open-Label Study

K. Tashiro, H. Sasaki, I. Yabe, 2004, Clinical neuropharmacology.

Syringomyelia as a cause of body hypertrophy

S. Kikuchi, K. Tashiro, I. Yabe, 1996, The Lancet.

Recessively inherited spastic paraplegia associated with ataxia, congenital cataracts, thin corpus callosum and axonal neuropathy

S. Kikuchi, K. Tashiro, H. Sasaki, 2000, Acta neurologica Scandinavica.

Identification of plasma microRNA expression changes in multiple system atrophy and Parkinson’s disease

H. Sasaki, I. Yabe, Jun Utsumi, 2019, Molecular Brain.

Brain SPECT analysis by 3D-SSP and phenotype of Parkinson's disease

S. Kikuchi, K. Tashiro, H. Sasaki, 2006, Journal of the Neurological Sciences.

Skin biopsies for diagnosing neuronal intranuclear inclusion disease: A retrospective study of 12 cases

Y. Matsuno, I. Yabe, H. Ujiie, 2023, The Journal of dermatology.

FDG-PET SUV can distinguish between spinal sarcoidosis and myelopathy with canal stenosis

S. Terae, T. Shiga, H. Sasaki, 2011, Journal of Neurology.

Reliability of the Japanese version of the Berg balance scale.

H. Sasaki, I. Yabe, M. Hirotani, 2014, Internal medicine.

Genome-wide association study identifies a new susceptibility locus in PLA2G4C for Multiple System Atrophy.

Sonja W. Scholz, A. Singleton, Y. Kusakabe, 2023, medRxiv.

Current status and challenges of neurosurgical procedures for patients with myelomeningocele in real-world Japan

M. Nonaka, I. Yabe, A. Asai, 2022, Child's Nervous System.

Efficacy and safety of leuprorelin in patients with spinal and bulbar muscular atrophy (JASMITT study): a multicentre, randomised, double-blind, placebo-controlled trial

S. Tsuji, G. Sobue, M. Morita, 2010, The Lancet Neurology.

Adult Leigh Disease Without Failure to Thrive

S. Saitoh, H. Sasaki, I. Yabe, 2011, The neurologist.

Neuropathological and molecular studies of spinocerebellar ataxia type 6 (SCA6)

H. Sawa, K. Tashiro, H. Sasaki, 1998, Acta Neuropathologica.

Mosaicism of unstable CAG repeats in the brain of spinocerebellar ataxia type 2

K. Tashiro, H. Sasaki, I. Yabe, 1999, Journal of Neurology.

Investigating the role of genetic counseling in neuromuscular disease considering life events

H. Sasaki, N. Hashimoto, I. Yabe, 2019, Journal of Human Genetics.

Usefulness of the Scale for Assessment and Rating of Ataxia (SARA)

H. Sasaki, H. Soma, I. Yabe, 2008, Journal of the Neurological Sciences.

Elderly patients with suspected Charcot-Marie-Tooth disease should be tested for the TTR gene for effective treatments

M. Nakagawa, H. Ishiura, J. Mitsui, 2022, Journal of Human Genetics.

Clinical trial of acetazolamide in SCA6, with assessment using the Ataxia Rating Scale and body stabilometry

K. Tashiro, H. Sasaki, I. Yabe, 2001, Acta neurologica Scandinavica.

Genetic polymorphisms of osteopontin in association with multiple sclerosis in Japanese patients

S. Kikuchi, K. Tashiro, I. Yabe, 2003, Journal of Neuroimmunology.

Unusual retinal phenotypes in an SCA7 family.

H. Sasaki, H. Soma, I. Yabe, 2009, Internal medicine.

Time course of downbeat positioning nystagmus in familial hemiplegic migraine type 1 treated with acetazolamide

S. Fukuda, H. Sasaki, I. Yabe, 2016, Journal of the Neurological Sciences.

Attack-related severity: a key factor in understanding the spectrum of idiopathic inflammatory demyelinating disorders

S. Kikuchi, K. Tashiro, H. Sasaki, 2004, Journal of the Neurological Sciences.

Painless legs and moving toes from parasagittal meningioma

H. Sasaki, T. Kano, I. Yabe, 2012, Movement Disorders.

Clinical factors affecting evoked magnetic fields in patients with Parkinson's disease

M. Otsuki, H. Shiraishi, H. Sasaki, 2020, PloS one.

Clinical factors affecting evoked magnetic fields in patients with Parkinson’s disease

M. Otsuki, H. Shiraishi, H. Sasaki, 2020, bioRxiv.

Pearls & Oy-sters: Adult-Onset Alexander Disease With Transient Swelling of the Medulla Oblongata

Tomokatsu Yoshida, T. Harada, I. Yabe, 2021, Neurology.

Hyperintense putaminal rim at 1.5 T: prevalence in normal subjects and distinguishing features from multiple system atrophy

H. Shirato, S. Terae, H. Sasaki, 2012, BMC Neurology.

Multiple system atrophy in Hokkaido, Japan: a prospective registry study of natural history and symptom assessment scales followed for 5 years

S. Shimohama, A. Tamakoshi, H. Uesugi, 2021, BMJ Open.

Pathology of frontotemporal dementia with limb girdle muscular dystrophy caused by a DNAJB6 mutation

Y. Hayashi, S. Hatakeyama, H. Sasaki, 2014, Clinical Neurology and Neurosurgery.

Brain activation during detrusor overactivity in patients with Parkinson's disease: a positron emission tomography study.

Tohru Shiga, Nagara Tamaki, Tsuyoshi Furuno, 2006, The Journal of urology.

Efficacy of intravenous cyclophosphamide therapy for neuromyelitis optica spectrum disorder.

H. Sasaki, H. Yaguchi, I. Yabe, 2013, Internal medicine.

Dissociation of smooth pursuit and vestibulo-ocular reflex cancellation in SCA-6

K Fukushima, Y Inuyama, K. Fukushima, 2000, Neurology.

Heredity in multiple system atrophy

Naoto Fujiki, H. Sasaki, H. Soma, 2006, Journal of the Neurological Sciences.

Relations of clinical symptoms with dopamine transporter imaging in drug-naïve Parkinson’s disease

S. Terae, H. Yaguchi, I. Yabe, 2020, Clinical Neurology and Neurosurgery.

Relation of overactive bladder with motor symptoms and dopamine transporter imaging in drug-naïve Parkinson's disease.

S. Terae, H. Yaguchi, I. Yabe, 2018, Parkinsonism & related disorders.

Comparison of Different Symptom Assessment Scales for Multiple System Atrophy

K. Oba, H. Sasaki, I. Yabe, 2015, The Cerebellum.

Scapular winging as a symptom of cervical flexion myelopathy.

J. Tashiro, H. Sasaki, H. Yaguchi, 2007, Internal medicine.

Estrogen receptor gene polymorphism and multiple sclerosis in Japanese patients: interaction with HLA-DRB1*1501 and disease modulation

S. Kikuchi, K. Tashiro, I. Yabe, 2002, Journal of Neuroimmunology.

C–C chemokine receptor 2 gene polymorphism in Japanese patients with multiple sclerosis

S. Kikuchi, K. Tashiro, I. Yabe, 2003, Journal of Neuroimmunology.

Epidemiology of Multiple System Atrophy in Hokkaido, the Northernmost Island of Japan

M. Nojima, M. Mori, H. Sasaki, 2015, The Cerebellum.

Correlation of active contact location with weight gain after subthalamic nucleus deep brain stimulation: a case series

M. Otsuki, K. Houkin, T. Shiga, 2021, BMC Neurology.

Correlation of antero-dorsal active contact location with weight gain after subthalamic nucleus deep brain stimulation: a case series

M. Otsuki, K. Houkin, T. Shiga, 2021 .

Copy number loss of (src homology 2 domain containing)-transforming protein 2 (SHC2) gene: discordant loss in monozygotic twins and frequent loss in patients with multiple system atrophy

M. Emi, H. Sasaki, Hidenori Sato, 2011, Molecular Brain.

Neck rigidity as a physical manifestation of higher brain hypo-function/dysfunction.

M. Otsuki, K. Tashiro, I. Yabe, 2011, In vivo.

Writing errors as a result of frontal dysfunction in Japanese patients with amyotrophic lateral sclerosis

M. Otsuki, Itaru Tamura, H. Sasaki, 2010, Journal of Neurology.

High-dose ubiquinol supplementation in multiple-system atrophy: a multicentre, randomised, double-blinded, placebo-controlled phase 2 trial

N. Sawamoto, T. Matsukawa, R. Hanajima, 2023, EClinicalMedicine.

Genomic HLA profiles of MS in Hokkaido, Japan: important role of DPB1*0501 allele

S. Kikuchi, K. Tashiro, H. Sasaki, 2000, Journal of Neurology.

Anti-myelin oligodendrocyte glycoprotein antibody-associated encephalitis with cortical hyperintensity and pathologically confirmed extensive demyelination

Y. Shinmei, A. Nagai, H. Yaguchi, 2021, Neuroimmunology Reports.

An autopsy case of Sjögren's syndrome with acute encephalomyelopathy.

H. Sasaki, H. Yaguchi, T. Takeda, 2008, Internal medicine.

CTLA-4 gene polymorphism is not associated with conventional multiple sclerosis in Japanese

S. Kikuchi, H. Sasaki, I. Yabe, 2005, Journal of Neuroimmunology.

Genetic factors affecting survival in Japanese patients with sporadic amyotrophic lateral sclerosis: a genome-wide association study and verification in iPSC-derived motor neurons from patients

H. Okano, G. Sobue, Toshio Shimizu, 2023, Journal of Neurology, Neurosurgery, and Psychiatry.

Reliability of the Japanese version of the scales for outcomes in Parkinson's disease-autonomic questionnaire

H. Sasaki, T. Kano, I. Yabe, 2014, Clinical Neurology and Neurosurgery.

Brain 3D-SSP SPECT analysis in dementia with Lewy bodies, Parkinson's disease with and without dementia, and Alzheimer's disease

Kazuto Yoshida, S. Kikuchi, K. Tashiro, 2005, Clinical Neurology and Neurosurgery.

Serum melatonin levels and insomnia in patients with Machado-Joseph Disease

M. Okawa, H. Sasaki, I. Yabe, 2004 .

CSF pleocytosis and expansion of spinal lesions in Japanese Multiple sclerosis with special reference to the new diagnostic criteria

S. Kikuchi, K. Tashiro, H. Sasaki, 2005, Journal of Neurology.

Importance of T1-MRI enhanced pyramidal tracts in differential diagnosis as to paraneoplastic encephalomyelitis

H. Sasaki, H. Yaguchi, I. Yabe, 2015, Clinical Neurology and Neurosurgery.

Influence of urinary urgency and other urinary disturbances on falls in Parkinson's disease

S. Fukuhara, Y. Hayashino, H. Sasaki, 2016, Journal of the Neurological Sciences.

Late onset ataxia phenotype in dentatorubro-pallidoluysian atrophy (DRPLA)

S. Kikuchi, K. Tashiro, F. Moriwaka, 2002, Journal of Neurology.

Hashimoto's encephalopathy mimicking a brain tumor and its pathological findings: A case report

H. Sasaki, T. Kano, I. Yabe, 2018, Journal of the Neurological Sciences.

The Responsiveness of Triaxial Accelerometer Measurement of Gait Ataxia Is Higher than That of the Scale for the Assessment and Rating of Ataxia in the Early Stages of Spinocerebellar Degeneration

K. Takakusaki, H. Sasaki, I. Yabe, 2019, The Cerebellum.

Validity and reliability of a pilot scale for assessment of multiple system atrophy symptoms

H. Sasaki, T. Kano, I. Yabe, 2017, Cerebellum & Ataxias.

Different surgical treatment techniques used by neurosurgeons and orthopedists for syringomyelia caused by Chiari I malformation in Japan.

R. Uehara, H. Sasaki, K. Hida, 2013, Journal of neurosurgery. Spine.

Novel partial deletions, frameshift and missense mutations of CSF1R in patents with CSF1R‐related leukoencephalopathy

A. Miyashita, N. Hara, T. Ikeuchi, 2023, European journal of neurology.

[A case of paraneoplastic myelopathy associated with anti-CV2/CRMP5 antibodies with small-cell lung cancer].

H. Sasaki, T. Kano, I. Yabe, 2020, Rinsho shinkeigaku = Clinical neurology.

Brain Regions Associated With Cognitive Impairment in Patients With Parkinson Disease: Quantitative Analysis of Cerebral Blood Flow Using 123I Iodoamphetamine SPECT

T. Shiga, N. Tamaki, K. Hirata, 2013, Clinical nuclear medicine.

The Efficacy of Istradefylline for Treating Mild Wearing-Off in Parkinson Disease

M. Kitagawa, H. Sasaki, I. Yabe, 2017, Clinical neuropharmacology.

Baló's concentric sclerosislike lesion in the brainstem of a multiple sclerosis patient

S. Kikuchi, H. Sasaki, I. Yabe, 2008, Journal of Neurology.

Usefulness of 11C-methionine-positron emission tomography for the diagnosis of progressive multifocal leukoencephalopathy

T. Shiga, M. Saijo, H. Sasaki, 2014, Journal of Neurology.

Chronic inflammatory demyelinating polyneuropathy after treatment with interferon-alpha.

H. Sasaki, I. Yabe, M. Hirotani, 2009, Internal medicine.

Long-term Outcome of Adenosine A2A Receptor Antagonist on Lower Urinary Tract Symptoms in Male Parkinson Disease Patients

N. Shinohara, H. Sasaki, I. Yabe, 2018, Clinical neuropharmacology.

Efficacy of Intravenous Immunoglobulins against Chronic Lymphocytic Inflammation with Pontine Perivascular Enhancement Responsive to Steroids: A Case Report

I. Yabe, S. Ura, Takumi Tsuchida, 2023, Case reports in neurology.

SCA6 mutation analysis in a large cohort of the Japanese patients with late-onset pure cerebellar ataxia

A. Ohnishi, K. Tashiro, H. Sasaki, 1998, Journal of the Neurological Sciences.

Beneficial effects of tandospirone on ataxia of a patient with Machado‐Joseph disease

K. Tashiro, I. Yabe, A. Takei, 2002, Psychiatry and clinical neurosciences.

Relationships of drooling with motor symptoms and dopamine transporter imaging in drug-naïve Parkinson’s disease

S. Terae, H. Yaguchi, I. Yabe, 2020, Clinical Neurology and Neurosurgery.

Smoking and younger age at onset in anti-acetylcholine receptor antibody-positive myasthenia gravis

S. Kikuchi, I. Yabe, K. Sakushima, 2022, Immunological medicine.

Downbeat positioning nystagmus is a common clinical feature despite variable phenotypes in an FHM1 family

S. Saitoh, M. Kitagawa, H. Sasaki, 2008, Journal of Neurology.

‘Drug holiday’ effects of tandospirone in a patient with Machado–Joseph disease

K. Tashiro, I. Yabe, A. Takei, 2003, Psychiatry and clinical neurosciences.

Instructions for use Title Pathology of frontotemporal dementia with limb girdlemuscular dystrophy caused by a DNAJB 6 mutation

Y. Hayashi, S. Hatakeyama, H. Sasaki, 2016 .

Assessment for the timing of comprehensive genomic profiling tests in patients with advanced solid cancers

Y. Matsuno, H. Dosaka-akita, A. Manabe, 2023, Cancer science.

Identification of plasma microRNA expression changes in multiple system atrophy and Parkinson’s disease

H. Sasaki, I. Yabe, Jun Utsumi, 2019, Molecular Brain.

Clinical features of spinal cord sarcoidosis: analysis of 17 neurosarcoidosis patients

H. Sasaki, I. Yabe, K. Sakushima, 2011, Journal of Neurology.

Genetic Creutzfeldt‒Jakob disease with 5-octapeptide repeats presented as frontotemporal dementia

H. Mizusawa, F. Moriwaka, K. Satoh, 2023, Human Genome Variation.

Cardiac involvement with anti‐mitochondrial antibody‐positive myositis mimicking cardiac sarcoidosis

A. Nagai, T. Nagai, T. Anzai, 2020, ESC heart failure.

Multimodal Imaging Finding In Unverricht-Lundborg Disease

T. Shiga, N. Tanaka, F. Takeuchi, 2004 .

Estrogen receptor gene polymorphism and multiple sclerosis in Japanese patients: interaction with HLA-DRB1*1501 and disease modulation

S. Kikuchi, K. Tashiro, I. Yabe, 2002, Journal of Neuroimmunology.

An assessment of the association between IL-2 gene polymorphisms and Japanese patients with multiple sclerosis

S. Kikuchi, K. Tashiro, I. Yabe, 2002, Journal of the Neurological Sciences.

[A case of successful treatment of brain and lung cryptococcosis caused by Cryptococcus gattii].

T. Umeyama, H. Sasaki, T. Kano, 2012, Rinsho shinkeigaku = Clinical neurology.

Efficacy of Quantitative Susceptibility Mapping with Brain Surface Correction and Vein Removal for Detecting Increase Magnetic Susceptibility in Patients with Alzheimer’s Disease

N. Matsukawa, M. Sasaki, K. Kudo, 2022, Magnetic resonance in medical sciences : MRMS : an official journal of Japan Society of Magnetic Resonance in Medicine.

Clinical characterization and successful treatment of 6 patients with Churg–Strauss syndrome-associated neuropathy

H. Sasaki, H. Yaguchi, I. Yabe, 2009, Clinical Neurology and Neurosurgery.

Spinocerebellar ataxia type 14 family with a novel PRKCG mutation

H. Sasaki, I. Yabe, I. Takahashi, 2016 .

Mapping of autosomal dominant cerebellar ataxia without the pathogenic PPP2R2B mutation to the locus for spinocerebellar ataxia 12.

S. Tsuji, Y. Fukuda, H. Sasaki, 2010, Archives of neurology.

Clinical features of spinal cord sarcoidosis: analysis of 17 neurosarcoidosis patients

H. Sasaki, I. Yabe, K. Sakushima, 2011, Journal of Neurology.

FDG-PET SUV can distinguish between spinal sarcoidosis and myelopathy with canal stenosis

S. Terae, T. Shiga, H. Sasaki, 2011, Journal of Neurology.

FDG-PET SUV can distinguish between spinal sarcoidosis and myelopathy with canal stenosis

I. Yabe, 2020 .

Fdg-pet Suv Can Distinguish between Spinal Sarcoidosis and Myelopathy with Canal Sakushima Et Al, Page 2

S. Terae, H. Sasaki, I. Yabe, 2022 .

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.

Abnormal brain MRI signals in the splenium of the corpus callosum, basal ganglia and internal capsule in a suspected case with tuberculous meningitis.

S. Kikuchi, H. Sasaki, I. Yabe, 2007, Internal medicine.

Writing errors in ALS related to loss of neuronal integrity in the anterior cingulate gyrus

M. Otsuki, T. Shiga, N. Tamaki, 2012, Journal of the Neurological Sciences.

[Periodic alternating nystagmus in spinocerebellar ataxia type 6 (SCA 6)].

K. Tashiro, H. Sasaki, I. Yabe, 1998, Rinsho shinkeigaku = Clinical neurology.

Investigating the role of genetic counseling in neuromuscular disease considering life events

H. Sasaki, N. Hashimoto, I. Yabe, 2019, Journal of Human Genetics.

[National survey of presymptomatic genetic testing for adult-onset hereditary neuromuscular diseases-system development for after the establishment of therapies].

K. Oda, Katsuya Nakamura, Y. Sekijima, 2022, Rinsho shinkeigaku = Clinical neurology.

[Two elderly cases of transthyretin amyloid polyneuropathy without a family history].

H. Sasaki, I. Yabe, M. Matsushima, 2020, Rinsho shinkeigaku = Clinical neurology.