M. Nakagawa

T. Tokuda, M. Nakagawa, M. Mori, 2011, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

Collagen VI deficiency in Ullrich's disease

K. Arimura, M. Nakagawa, M. Osame, 2001, Annals of neurology.

Altered T cell phenotypes associated with clinical relapse of multiple sclerosis patients receiving fingolimod therapy

R. Takahashi, M. Nakagawa, T. Mizuno, 2016, Scientific Reports.

A case of acute‐onset multifocal motor neuropathy after Mycoplasma infection

M. Nakagawa, T. Mizuno, T. Ohara, 2018, Muscle & nerve.

Optinurin inclusions in proximal hereditary motor and sensory neuropathy (HMSN-P): familial amyotrophic lateral sclerosis with sensory neuronopathy?

M. Nakagawa, 2011, Journal of Neurology, Neurosurgery & Psychiatry.

Molecular analysis of hereditary deficiency of the third component of complement (C3) in two sisters.

M. Nakagawa, H. Takashima, M. Osame, 2001, Internal medicine.

Genetic spectrum of Charcot–Marie–Tooth disease associated with myelin protein zero gene variants in Japan

S. Tsuji, N. Hattori, T. Hatano, 2020, Clinical genetics.

Analysis of neural crest cells from Charcot–Marie–Tooth disease patients demonstrates disease-relevant molecular signature

J. Toguchida, Takuya Yamamoto, M. Nakagawa, 2017, Neuroreport.

Rate of Changes in CMT Neuropathy and Examination Scores in Japanese Adult CMT1A Patients

K. Shiga, M. Nakagawa, I. Mizuta, 2020, Frontiers in Neurology.

Adult-onset leukoencephalopathy with homozygous LAMB1 missense mutation

Tomokatsu Yoshida, M. Nakagawa, K. Tashiro, 2020, Neurology: Genetics.

Renal involvement in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).

Y. Mori, M. Nakagawa, K. Sonomura, 2007, Clinical nephrology.

Clinical and genetic diversities of Charcot‐Marie‐Tooth disease with MFN2 mutations in a large case study

S. Tsuji, S. Morishita, M. Nakagawa, 2017, Journal of the peripheral nervous system : JPNS.

Refinement of a locus for autosomal dominant hereditary motor and sensory neuropathy with proximal dominancy (HMSN-P) and genetic heterogeneity

Katsuhito Yasuno, G. Tamiya, R. Kaji, 2007, Journal of Human Genetics.

Gene for hereditary motor and sensory neuropathy (proximal dominant form) mapped to 3q13.1

J. Terwilliger, M. Nakagawa, H. Takashima, 1999, Neuromuscular Disorders.

HTLV-I-associated myelopathy: analysis of 213 patients based on clinical features and laboratory findings.

K. Arimura, M. Nakagawa, S. Izumo, 1995, Journal of neurovirology.

Inflammatory myofibroblastic tumor of the cerebellar hemisphere--case report.

M. Nakagawa, H. Ujiié, Koichi Kato, 2011, Neurologia medico-chirurgica.

Higher Levels of Streptococcus in Upper Gastrointestinal Mucosa Associated with Symptoms in Patients with Functional Dyspepsia

Y. Naito, K. Kamada, M. Nakagawa, 2019, Digestion.

Phenøtypes and mitochondrial DNA substitutions in families with A3243G mutation

M. Nakagawa, M. Osame, I. Higuchi, 2002, Acta neurologica Scandinavica.

Retinal manifestations in mitochondrial diseases associated with mitochondrial DNA mutation.

M. Nakagawa, N. Ohba, Y. Isashiki, 1998, Acta ophthalmologica Scandinavica.

In situ polymerase chain reaction detection of HTLV-I provirus and expression of the p53 tumor suppressor gene in infiltrating cells in skeletal muscle from a patient with adult T cell leukemia

M. Nakagawa, S. Izumo, M. Osame, 2004, Acta Neuropathologica.

Phenotypes of X-linked Charcot-Marie-Tooth disease and altered trafficking of mutant Connexin 32 (GJB1)

M. Nakagawa, H. Takashima, T. Moritoyo, 2001, Journal of Human Genetics.

Sixty Six–Month Follow-up of Muscle Power and Respiratory Function in a Case With Adult-Type Pompe Disease Treated With Enzyme Replacement Therapy

N. Kuriyama, K. Shiga, M. Nakagawa, 2014, Journal of clinical neuromuscular disease.

A case of cerebral aquaporinopathy

K. Shiga, M. Nakagawa, T. Yoshida, 2010, Multiple sclerosis.

Evaluation of Factors Associated With Elevated Levels of Platelet-Derived Microparticles in the Acute Phase of Cerebral Infarction

N. Kuriyama, T. Tokuda, Kei Yamada, 2010, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Facioscapulohumeral muscular dystrophy: clinical diversity and genetic abnormalities in Japanese patients.

K. Arimura, M. Nakagawa, M. Osame, 1997, Internal medicine.

Familial facioscapulohumeral muscular dystrophy: phenotypic diversity and genetic abnormality

M. Nakagawa, Y. Isashiki, M. Osame, 1996, Acta neurologica Scandinavica.

HAM/TSP: recent perspectives in Japan.

K. Arimura, M. Nakagawa, S. Izumo, 1996, Journal of acquired immune deficiency syndromes and human retrovirology : official publication of the International Retrovirology Association.

Transendocytosis is impaired in CADASIL-mutant NOTCH3

Masaki Tanaka, Yoshihisa Watanabe, M. Nakagawa, 2012, Experimental Neurology.

Extracellular neurosin degrades α-synuclein in cultured cells

Masaki Tanaka, Yoshihisa Watanabe, T. Tokuda, 2010, Neuroscience Research.

Identification of TIGIT as an HBZ-induced gene by genome-wide analyses: its association with evasion of host defense

Yutaka Suzuki, M. Matsuoka, J. Yasunaga, 2015, Retrovirology.

An Adult Case of Anti-Myelin Oligodendrocyte Glycoprotein (MOG) Antibody-associated Multiphasic Acute Disseminated Encephalomyelitis at 33-year Intervals.

M. Nakagawa, Y. Kushimura, T. Mizuno, 2016, Internal medicine.

Month of birth in multiple sclerosis with and without longitudinally extensive spinal cord lesions: A study of a Japanese national survey

J. Kira, M. Kinoshita, M. Nakagawa, 2013, Journal of the Neurological Sciences.

Different manners of sarcoglycan expression in genetically proven α-sarcoglycan deficiency and γ-sarcoglycan deficiency

K. Arimura, M. Nakagawa, M. Osame, 1998, Acta Neuropathologica.

Different manners of sarcoglycan expression in genetically proven alpha-sarcoglycan deficiency and gamma-sarcoglycan deficiency.

K. Arimura, M. Nakagawa, M. Osame, 1998, Acta Neuropathologica.

Miyoshi myopathy patients with novel 5' splicing donor site mutations showed different dysferlin immunostaining at the sarcolemma

M. Nakagawa, Toshiaki Takahashi, M. Aoki, 2002, Acta Neuropathologica.

Type II muscle fibers are stained by anti-Fas antibody

M. Nakagawa, M. Osame, I. Higuchi, 1995, Journal of the Neurological Sciences.

Phylogenetic subgroups of human T cell lymphotropic virus (HTLV) type I in the tax gene and their association with different risks for HTLV-I-associated myelopathy/tropical spastic paraparesis.

M. Nakagawa, M. Yamashita, S. Izumo, 2000, The Journal of infectious diseases.

Therapeutic trials in 200 patients with HTLV-I-associated myelopathy/ tropical spastic paraparesis.

K. Arimura, M. Nakagawa, S. Izumo, 1996, Journal of neurovirology.

An oligodeoxyribonucleotide-directed dual amber method for site-directed mutagenesis.

M. Nakagawa, T. Hashimoto-Gotoh, Y. Ogasahara, 1995, Gene.

Evaluation of autonomic malfunction in HTLV-1 associated myelopathy (HAM)

N. Kuriyama, T. Tokuda, Kei Yamada, 2009, Autonomic Neuroscience.

M. Nakagawa, M. Osame, I. Higuchi, 1994, Internal medicine.

Renin-angiotensin system gene polymorphism in Japanese stroke patients

K. Yoshikawa, K. Shiga, M. Nakagawa, 2003 .

Striatocapsular infarction associated with middle cerebral artery disease

M. Nakagawa, T. Ohara, Yasumasa Yamamoto, 2010 .

An autopsy case of peripheral neuroepithelioma in posterior mediastinum with p53 point mutation.

M. Nakagawa, M. Osame, K. Mizuno, 1998, Internal medicine.

Three patients with posterior cerebral artery infarction occurring during migraine attack: An investigation by digital subtraction angiography

M. Nakagawa, A. Hosomi, H. Tenjin, 2008 .

Autosomal dominant leukodystrophy with axonal spheroids and pigmented glia: clinical and neuropathological characteristics

K. Shiga, M. Nakagawa, M. Muranishi, 2005, Acta Neuropathologica.

Sjögren syndrome presenting with encephalopathy mimicking Creutzfeldt–Jakob disease

M. Nakagawa, T. Mizuno, C. Fujii, 2013, Journal of the Neurological Sciences.

Experimental germanium myopathy

M. Nakagawa, S. Izumo, M. Osame, 2004, Acta Neuropathologica.

Experimental simvastatin-induced myopathy in rabbits

K. Arimura, M. Nakagawa, M. Osame, 1992, Journal of the Neurological Sciences.

IMMUNOHISTOCHEMICAL STUDY OF CYTOCHROME COXIDASE WITH A MONOCLONAL ANTIBODY IN MITOCHONDRIAL MYOPATHY

M. Nakagawa, M. Osame, I. Higuchi, 1988 .

A monoclonal antibody against cytochrome c oxidase distinguishes cardiac and skeletal muscle mitochondria.

M. Nakagawa, A. Miranda, 1987, Experimental cell research.

Human T-cell lymphotropic virus type I (HTLV-I)-related clinical and laboratory findings for HTLV-I-infected blood donors.

M. Nakagawa, S. Izumo, M. Osame, 2003, Journal of acquired immune deficiency syndromes.

Clinical course of HTLV-I-associated uveitis.

M. Nakagawa, N. Ohba, K. Nakao, 1999, Japanese journal of ophthalmology.

Interferon-alpha is effective in HTLV-I-associated myelopathy

Y. Itoyama, M. Nakagawa, S. Izumo, 1996, Neurology.

Characteristic expression of cell adhesion molecules in adhalin deficiency

K. Arimura, M. Nakagawa, M. Osame, 1996, Journal of the Neurological Sciences.

Familial spastic paraplegia with mental impairment and thin corpus callosum

A. Nakamura, M. Nakagawa, S. Izumo, 1995, Journal of the Neurological Sciences.

Dysferlin mutations in Japanese Miyoshi myopathy

Y. Itoyama, I. Nonaka, Kayoko Saito, 2003, Neurology.

Choroideremia with leukoencephalopathy and arylsulfatase A pseudodeficiency

M. Nakagawa, M. Osame, S. Ijichi, 1996, Journal of the Neurological Sciences.

Application of Ion-beam Implanted Expanded Polytetrafluoroethylene to Microvascular Decompression and the Surgical Outcome

M. Nakagawa, H. Ujiié, A. Teramoto, 2017, Neurologia medico-chirurgica.

Determination of urine thiocyanate in patients with amyotrophic lateral sclerosis

M. Nakagawa, S. Izumo, M. Osame, 1984, Acta neurologica Scandinavica.

[A case of noninvasive sinus aspergillosis showing orbital apex syndrome].

Tomokatsu Yoshida, M. Nakagawa, R. Isayama, 2011, Rinsho shinkeigaku = Clinical neurology.

Neuronal ceroid-lipofuscinosis in a Japanese domestic shorthair cat.

M. Nakagawa, J. Yamate, M. Kuwamura, 2009, The Journal of veterinary medical science.

Cerebrospinal fluid proteomic patterns discriminate Parkinson's disease and multiple system atrophy

Masanori Nakagawa, Masaya Ikegawa, Herbert Thiele, 2012, Movement disorders : official journal of the Movement Disorder Society.

Atypical rigid form of Huntington's disease: a case with peripheral amyotrophy and congenital defects of a lower limb.

M. Nakagawa, N. Kanzato, T. Matsuzaki, 1998, Internal medicine.

Clinicopathological features of neuropathy associated with lymphoma.

G. Sobue, M. Nakagawa, M. Tomita, 2013, Brain : a journal of neurology.

Demyelinating and axonal features of Charcot-Marie-Tooth disease with mutations of myelin-related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patients.

G. Sobue, K. Nakashima, J. Kira, 2003, Brain : a journal of neurology.

Screening of SLC25A13 mutations in early and late onset patients with citrin deficiency and in the Japanese population: Identification of two novel mutations and establishment of multiple DNA diagnosis methods for nine mutations

T. Saheki, M. Nakagawa, Keiko Kobayashi, 2002, Human mutation.

Fatal infantile cytochrome c oxidase deficiency

N. Bresolin, S. Dimauro, M. Zeviani, 1985, Neurology.

Phenotypic variation in a large Japanese family with Miyoshi myopathy with nonsense mutation in exon 19 of dysferlin gene

M. Nakagawa, H. Takashima, K. Goto, 2001, Journal of the Neurological Sciences.

Amyloid myopathy: a therapeutic trial for the rare and underdiagnosed myopathy with bortezomib

T. Tokuda, K. Shiga, M. Nakagawa, 2010, Journal of Neurology.

Optic neuropathy and cerebellar ataxia associated with a rare missense variation (A14510G) of mitochondrial DNA

M. Nakagawa, N. Ohba, Y. Isashiki, 2001, The British journal of ophthalmology.

Isolation of a cDNA clone encoding subunit IV of human cytochrome c oxidase.

M. I. Lomax, S. Dimauro, E. Schon, 1987, Gene.

Cytochrome c oxidase deficiency.

N. Bresolin, S. Dimauro, M. Zeviani, 1985, Biochemical Society transactions.

Towards genomic database of Alexander disease to identify variations modifying disease phenotype

Tomokatsu Yoshida, M. Nakagawa, K. Tashiro, 2019, Scientific Reports.

HTLV-1 bZIP Factor Impairs Anti-viral Immunity by Inducing Co-inhibitory Molecule, T Cell Immunoglobulin and ITIM Domain (TIGIT)

Yutaka Suzuki, M. Matsuoka, J. Yasunaga, 2016, PLoS pathogens.

Fine mapping of 16q-linked autosomal dominant cerebellar ataxia type III in Japanese families

K. Arimura, M. Nakagawa, R. Hirano, 2004, Neurogenetics.

Overexpression of ter94, Drosophila VCP, improves motor neuron degeneration induced by knockdown of TBPH, Drosophila TDP-43.

H. Yoshida, T. Tokuda, M. Yamaguchi, 2018, American journal of neurodegenerative disease.

Mutations in COA7 cause spinocerebellar ataxia with axonal neuropathy

S. Tsuji, S. Morishita, M. Yamaguchi, 2018, Brain : a journal of neurology.

Autosomal dominant early onset dementia and leukoencephalopathy in a Japanese family: clinical, neuroimaging and genetic studies

K. Arimura, M. Nakagawa, M. Nagai, 1997, Journal of the Neurological Sciences.

TGF-beta1 is associated with the progression of intracranial deep white matter lesions: a pilot study with 5 years of magnetic resonance imaging follow-up

N. Kuriyama, Kei Yamada, Y. Nagakane, 2014, Neurological research.

Effect of Lomerizine Hydrochloride on Preventing Strokes in Patients With Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy.

Kei Yamada, M. Nakagawa, I. Yokota, 2020, Clinical neuropharmacology.

Simultaneous Impairment of Intracranial and Peripheral Artery Vasoreactivity in CADASIL Patients

N. Kuriyama, T. Tokuda, Y. Nagakane, 2011, Cerebrovascular Diseases.

Cognitive impairment and cerebral hypoperfusion in a CADASIL patient improved during administration of lomerizine.

T. Tokuda, Y. Nagakane, M. Nakagawa, 2009, Clinical neuropharmacology.

The main HTLV-I-harboring cells in the muscles of viral carriers with polymyositis are not macrophages but CD4+ lymphocytes

K. Arimura, M. Nakagawa, R. Rosales, 1996, Acta Neuropathologica.

Detection of HTLV‐I provirus by in situ polymerase chain reaction in mononuclear inflammatory cells in skeletal muscle of viral carriers with polymyositis

K. Arimura, M. Nakagawa, S. Izumo, 1995, Muscle & nerve.

Title HTLV-1 bZIP Factor Impairs Anti-viral Immunity by Inducing Co-inhibitory Molecule, T Cell Immunoglobulin and ITIM

Yutaka Suzuki, M. Matsuoka, J. Yasunaga, 2019 .

Efficacy of Corticosteroid Therapy for HTLV-1-Associated Myelopathy: A Randomized Controlled Trial (HAMLET-P)

N. Araya, M. Nakagawa, M. Bland, 2022, Viruses.

Capillary changes in skeletal muscle of patients with Ullrich's disease with collagen VI deficiency

K. Arimura, M. Nakagawa, T. Hashiguchi, 2003, Acta Neuropathologica.

Increased α-synuclein levels in the cerebrospinal fluid of patients with Creutzfeldt–Jakob disease

T. Tokuda, M. Nakagawa, O. El‐Agnaf, 2014, Journal of Neurology.

Decreased α-synuclein in cerebrospinal fluid of aged individuals and subjects with Parkinson’s disease.

T. Tokuda, J. Locascio, D. Allsop, 2006 .

Cross-Sectional Analysis of Neurological Findings among Healthy Elderly: Study in a Remote Island in Kagoshima, Japan

S. Akiba, K. Arimura, M. Nakagawa, 2001, Neuroepidemiology.

[Hypertrophic pachymeningitis associated with autoimmune pancreatitis examined for IgG4 related disease: a case report].

M. Nakagawa, H. Ujiié, Y. Tamano, 2011, No shinkei geka. Neurological surgery.

[A case of MPO-ANCA positive hypertrophic pachymeningitis associated with vascular inflammation in the kidney biopsy].

Tomokatsu Yoshida, M. Nakagawa, T. Mizuno, 2015, Rinsho shinkeigaku = Clinical neurology.

HTLV-I-associated myelopathy (HAM): epidemiology, clinical features, and pathomechanism

I. Maruyama, K. Arimura, M. Nakagawa, 1992 .

Polymyositis with atypical pathological features associated with thymic carcinoma.

K. Shiga, M. Nakagawa, Y. Azuma, 2009, Internal medicine.

Frameshift mutation in the collagen VI gene causes Ullrich's disease

K. Arimura, M. Nakagawa, T. Hashiguchi, 2001, Annals of neurology.

Cardiac involvement in mitochondrial diseases. A study on 17 patients with documented mitochondrial DNA defects.

M. Miyata, M. Nakagawa, M. Osame, 1995, Circulation.

Molecular mechanism of rigid spine with muscular dystrophy type 1 caused by novel mutations of selenoprotein N gene

K. Arimura, M. Nakagawa, R. Hirano, 2006, Neurogenetics.

Aβ levels in the jugular vein and high molecular weight Aβ oligomer levels in CSF can be used as biomarkers to indicate the anti-amyloid effect of IVIg for Alzheimer’s disease

T. Tokuda, D. Allsop, M. Taylor, 2017, PloS one.

KF-1 Ubiquitin Ligase: Anxiety Suppressor Model

M. Nakagawa, Y. Marunaka, T. Hashimoto-Gotoh, 2011, Cell Biochemistry and Biophysics.

An autopsy case of mitochondrial encephalomyopathy: biochemical and electron microscopic studies of the brain

M. Nakagawa, S. Matsukura, M. Kuriyama, 1988, Journal of the Neurological Sciences.

Leber's hereditary optic neuropathy: mitochondrial and biochemical studies on muscle biopsies.

M. Nakagawa, N. Ohba, M. Osame, 1987, The British journal of ophthalmology.

A new type of hereditary motor and sensory neuropathy linked to chromosome 3

K. Arimura, M. Nakagawa, S. Izumo, 1997, Annals of neurology.

SET binding factor 2 (SBF2) mutation causes CMT4B with juvenile onset glaucoma

M Nakagawa, J. Lupski, C. Boerkoel, 2004, Neurology.

Novel mutation at the initiation codon in the Norrie disease gene in two Japanese families

M. Nakagawa, N. Ohba, Y. Isashiki, 2004, Human Genetics.

Hereditary motor and sensory neuropathy with myelin folding and juvenile onset glaucoma

M. Nakagawa, K. Unoki, H. Takashima, 2000, Neurology.

Comparison of the myotonic dystrophy associated CTG repeat in European and Japanese populations.

T. Ogihara, R. Williamson, M. Nakagawa, 1992, Journal of medical genetics.

Predictive markers of blood cytokine and chemokine in recurrent brain infarction.

N. Kuriyama, T. Tokuda, Kei Yamada, 2009, Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research.

Analysis of CCG repeats in Huntingtin gene among HD patients and normal populations in Japan.

M. Nakagawa, A. Karami, M. Osame, 2008, Archives of medical research.

Steroid-responsive myalgia in a patient with Becker muscular dystrophy

Koichiro Nakamura, M. Nakagawa, M. Osame, 1993, Journal of the Neurological Sciences.

Intracranial deep white matter lesions (DWLs) are associated with chronic kidney disease (CKD) and cognitive impairment: a 5-year follow-up magnetic resonance imaging (MRI) study.

N. Kuriyama, E. Ozaki, M. Nakagawa, 2013, Archives of gerontology and geriatrics.

Mollaret cells detected in a patient with varicella-zoster virus meningitis

Tomokatsu Yoshida, M. Nakagawa, Y. Tomii, 2012, Clinical Neurology and Neurosurgery.

[Head drop syndrome in a patient with immune-mediated necrotizing myopathy with anti-signal recognition particle antibody: a case report].

K. Shiga, M. Nakagawa, Y. Kushimura, 2013, Rinsho shinkeigaku = Clinical neurology.

Pathological characteristics of skeletal muscle in Ullrich's disease with collagen VI deficiency

K. Arimura, M. Nakagawa, M. Osame, 2003, Neuromuscular Disorders.

Nerve ultrasound depicts peripheral nerve enlargement in patients with genetically distinct Charcot-Marie-Tooth disease

K. Shiga, M. Nakagawa, I. Mizuta, 2014, Journal of Neurology, Neurosurgery & Psychiatry.

Demyelinating features in sensory nerve conduction in Fisher syndrome.

K. Shiga, M. Nakagawa, C. Fujii, 2012, Internal medicine.

Neuro-Behçet disease mimicking brain tumor.

Kei Yamada, M. Nakagawa, K. Nakajima, 2005, AJNR. American journal of neuroradiology.

An Immunohistochemical Analysis of Gastric B-cell Lymphomas: Stromal Cells Exhibit Peculiar Histogenesis in Gastric B-cell Lymphomas

S. Akiyama, M. Nakagawa, S. Yonezawa, 2003 .

Application of short-time magnetic resonance examination for intervertebral disc diseases in dogs.

M. Nakagawa, K. Miyahara, K. Yamada, 2001, The Journal of veterinary medical science.

Microvascular endothelial abnormality in skeletal muscle from a patient with gastric cancer without dermatomyositis

K. Arimura, M. Nakagawa, M. Osame, 2000, Acta Neuropathologica.

Spreading of amyotrophic lateral sclerosis lesions—multifocal hits and local propagation?

Takayoshi Kobayashi, M. Nakagawa, S. Orimo, 2013, Journal of Neurology, Neurosurgery & Psychiatry.

High-density surface electromyography to assess motor unit firing rate in Charcot-Marie-Tooth disease type 1A patients

A. Holobar, Kohei Watanabe, M. Nakagawa, 2021, Clinical Neurophysiology.

Three cases of juvenile onset HTLV-I-associated myelopathy with pseudohypoparathyroidism

M. Nakagawa, M. Osame, K. Nakahara, 1993, Journal of the Neurological Sciences.

Cerebrotendinous xanthomatosis: cranial CT and MRI studies in eight patients

M. Nakagawa, M. Osame, M. Kuriyama, 2004, Neuroradiology.

Oculomotor nerve palsy evaluated by diffusion-tensor tractography

Masanori Nakagawa, Kei Yamada, Hirotoshi Ito, 2006, Neuroradiology.

A case of a dog with thickened calvaria with neurologic symptoms: magnetic resonance imaging (MRI) findings.

H. Furuoka, M. Nakagawa, T. Matsui, 1999, The Journal of veterinary medical science.

Total Tau Protein in Cerebrospinal Fluid and Diffusion-Weighted MRI as an Early Diagnostic Marker for Creutzfeldt-Jakob Disease

K. Eguchi, M. Nakagawa, A. Satoh, 2007, Dementia and Geriatric Cognitive Disorders.

[A case of Hashimoto's encephalopathy successfully treated with oral steroid therapy, resistant to high-dose methylprednisolone, plasma exchange and intravenous immunoglobulin].

K. Fukui, Y. Abe, M. Nakagawa, 2015, Rinshō shinkeigaku Clinical neurology.

Effects of peripheral lymphocyte subpopulations and the clinical correlation with Parkinson's disease

N. Kuriyama, J. Imanishi, M. Nakagawa, 2012, Geriatrics & gerontology international.

Anaplastic Astrocytoma Presenting as Reversible Posterior Leukoencephalopathy Syndrome

Tomokatsu Yoshida, M. Nakagawa, F. Niwa, 2006, The neurologist.

Subarachnoid hemorrhage caused by pilocytic astrocytoma--case report.

M. Nakagawa, H. Ujiié, Koichi Kato, 2011, Neurologia medico-chirurgica.

MR Imaging of Ventral Thalamic Nuclei

M. Nakagawa, K. Mineura, M. Nakagawa, 2010, American Journal of Neuroradiology.

Gene deletions in Japanese patients with Duchenne and Becker muscular dystrophy

M. Nakagawa, S. Yamaguchi, S. Tomatsu, 1990, Japanese Journal of Human Genetics.

Abnormal expression of laminin suggests disturbance of sarcolemma-extracellular matrix interaction in Japanese patients with autosomal recessive muscular dystrophy deficient in adhalin.

K. Campbell, S. Roberds, M. Nakagawa, 1994, The Journal of clinical investigation.

Detection of DNA fragmentation of myonuclei in myotonic dystrophy by double staining with anti-emerin antibody and by nick end-labeling

M. Nakagawa, M. Osame, I. Higuchi, 2000, Journal of the Neurological Sciences.

New missense mutation in the alpha-sarcoglycan gene in a Japanese patient with severe childhood autosomal recessive muscular dystrophy with incomplete alpha-sarcoglycan deficiency

K. Arimura, M. Nakagawa, M. Osame, 1997, Journal of the Neurological Sciences.

Immunocytochemical Analysis of the Cellular Infiltrate in the Spinal Cord Lesions in HTLV‐I‐Associated Myelopathy

M. Nakagawa, S. Izumo, M. Osame, 1993, Journal of neuropathology and experimental neurology.

CD62-mediated activation of platelets in cerebral white matter lesions in patients with cognitive decline.

N. Kuriyama, T. Tokuda, Kei Yamada, 2016, Archives of gerontology and geriatrics.

[Case of Charcot-Marie-Tooth disease type 1A with increased cerebrospinal fluid proteins and nerve root hypertrophy].

M. Nakagawa, M. Kondo, N. Ishigami, 2008, Rinsho shinkeigaku = Clinical neurology.

Dominantly inherited motor and sensory neuropathy with excessive myelin folding complex

M. Nakagawa, H. Yoshikawa, S. Izumo, 2004, Acta Neuropathologica.

Deletion in chromosome 17p11.2 including the peripheral myelin protein-22 (PMP-22) gene in hereditary neuropathy with liability to pressure palsies

K. Arimura, M. Nakagawa, S. Izumo, 1995, Journal of the Neurological Sciences.

Genome wide association study of HTLV-1–associated myelopathy/tropical spastic paraparesis in the Japanese population

T. Kawaguchi, M. Matsuoka, F. Matsuda, 2021, Proceedings of the National Academy of Sciences.

Mutations in the J domain of DNAJB6 cause dominant distal myopathy

E. Kerty, I. Nishino, M. Nakagawa, 2019, Neuromuscular Disorders.

Cleavage of normal and pathological forms of α-synuclein by neurosin in vitro

Yoshihisa Watanabe, T. Tokuda, F. Kametani, 2008, Neuroscience Letters.

[Normokalemic periodic paralysis lasting for two weeks: a severe form of sodium channelopathy with M1592V mutation].

K. Shiga, M. Nakagawa, I. Mizuta, 2014, Rinsho shinkeigaku = Clinical neurology.

Utilization of a multiple antigenic peptide as a calibration standard in the BAN50 single antibody sandwich ELISA for Aβ oligomers.

T. Tokuda, D. Allsop, M. Taylor, 2012, Biochemical and biophysical research communications.

High-molecular weight β-amyloid oligomers are elevated in cerebrospinal fluid of Alzheimer patients

T. Tokuda, D. Allsop, M. Nakagawa, 2010, Alzheimer's & Dementia.

Detection of elevated levels of α-synuclein oligomers in CSF from patients with Parkinson disease

T. Tokuda, M. Nakagawa, A. Tamaoka, 2010, Neurology.

Statistically significant differences in the number of CD24 positive muscle fibers and satellite cells between sarcoglycanopathy and age-matched Becker muscular dystrophy patients.

K. Arimura, M. Nakagawa, M. Osame, 1999, Internal medicine.

Mutations in MME cause an autosomal‐recessive Charcot–Marie–Tooth disease type 2

S. Tsuji, J. Kira, S. Morishita, 2016, Annals of neurology.

Further evidence for a major ancient mutation underlying myotonic dystrophy from linkage disequilibrium studies in the Japanese population

T. Miki, M. Nakagawa, Keith J. Johnson, 1998, Journal of Human Genetics.

Mitochondrial abnormalities in extraocular muscles in myotonic dystrophy

M. Nakagawa, N. Ohba, Y. Isashiki, 1989 .

A case of paternally inherited congenital myotonic dystrophy.

T. Miki, M. Nakagawa, T. Miki, 1994, Journal of medical genetics.

Characteristics of dynamic mutation in Japanese myotonic dystrophy

T. Ogihara, M. Nakagawa, T. Miki, 1994, Japanese Journal of Human Genetics.

Long Insular Artery Infarction: Characteristics of a Previously Unrecognized Entity

N. Kuriyama, Y. Nagakane, M. Nakagawa, 2014, American Journal of Neuroradiology.

Cerebrovascular disorders and genetic polymorphisms: mitochondrial DNA5178C is predominant in cerebrovascular disorders

S. Akiba, K. Arimura, M. Nakagawa, 2002, Journal of the Neurological Sciences.

Comparison of Transcranial Brain Tissue Perfusion Images Between Ultraharmonic, Second Harmonic, and Power Harmonic Imaging

M. Nakagawa, T. Mizuno, H. Furuhata, 2004, Stroke.

Association between Mid-Regional Proadrenomedullin Levels and Progression of Deep White Matter Lesions in the Brain Accompanying Cognitive Decline.

N. Kuriyama, T. Tokuda, Kei Yamada, 2017, Journal of Alzheimer's disease : JAD.

Neck weakness is a potent prognostic factor in sporadic amyotrophic lateral sclerosis patients

S. Tsuji, G. Sobue, M. Morita, 2013, Journal of Neurology, Neurosurgery & Psychiatry.

Contrasting echogenicity in flexor digitorum profundus–flexor carpi ulnaris: A diagnostic ultrasound pattern in sporadic inclusion body myositis

T. Tokuda, K. Shiga, M. Nakagawa, 2014, Muscle & nerve.

Mitochondrial DNA mutation correlates with stage progression and prognosis in non‐small cell lung cancer

Mitsuhiro Osame, Masanori Nakagawa, M. Nakagawa, 2003, Human mutation.

Acetazolamide vasoreactivity evaluated by transcranial power harmonic imaging and Doppler sonography.

Y. Nagakane, M. Nakagawa, T. Mizuno, 2008, Acta neurochirurgica. Supplement.

Quantitative evaluation of cerebrovascular reactivity in brain tissue by a refill kinetic method of transcranial ultrasonic perfusion imaging: a comparison with Doppler sonography.

K. Yoshikawa, M. Nakagawa, T. Mizuno, 2005, Acta neurochirurgica. Supplement.

Immunohistochemical Analysis of the Pathogenicity of Helicobacter pylori Infection: Excess Nitric Oxide Induced Indirectly by Lewis X and Y is the Cause of the Pathogenicity of Helicobacter pylori Infestation in the Stomach

M. Nakagawa, S. Yonezawa, E. Sato, 2002 .

Long-term follow-up study of health status in population living in methylmercury-polluted area.

T. Inaoka, T. Kitano, M. Nagano, 2005, Environmental sciences : an international journal of environmental physiology and toxicology.

CSF α-synuclein levels in dementia with Lewy bodies and Alzheimer's disease

T. Tokuda, M. Yoshita, M. Nakagawa, 2009, Brain Research.

Parasympathetic Dominant Autonomic Dysfunction in Charcot-Marie-Tooth Disease Type 2J with the MPZ Thr124Met Mutation.

K. Shiga, M. Nakagawa, I. Mizuta, 2015, Internal medicine.

Antibodies against human retinal proteins in serum from patients with cone dystrophy.

M. Nakagawa, N. Ohba, Y. Isashiki, 1992, Japanese journal of ophthalmology.

Compound muscle action potential duration ratio for differentiation between Charcot-Marie-Tooth disease and CIDP

M. Nakagawa, T. Mizuno, F. Kitani-Morii, 2022, Clinical Neurophysiology.

C2 Segmental Type of Vertebral Artery with Recurrent Embolic Strokes

K. Yoshikawa, Tomokatsu Yoshida, K. Shiga, 2005, Cerebrovascular Diseases.

Serial MRI changes in a patient with infantile Alexander disease and prolonged survival

T. Shiihara, Tomokatsu Yoshida, M. Nakagawa, 2011, Brain and Development.

Flow Velocity of the Superior Sagittal Sinus Is Reduced in Patients with Idiopathic Normal Pressure Hydrocephalus

N. Kuriyama, T. Tokuda, Kei Yamada, 2011, Journal of neuroimaging : official journal of the American Society of Neuroimaging.

High striatal amyloid beta-peptide deposition across different autosomal Alzheimer disease mutation types.

Masanori Nakagawa, Yasuyoshi Watanabe, Rachel Mulligan, 2009, Archives of neurology.

Leber's hereditary optic neuropathy: mitochondrial andbiochemical studies onmuscle biopsies

M. Nakagawa, N. Ohba, M. Osame, 2011 .

Adult onset limb-girdle type mitochondrial myopathy with a mitochondrial DNA np8291 A-to-G substitution

M. Nakagawa, M. Osame, I. Higuchi, 1999, Journal of Human Genetics.

[Cerebrotendinous xanthomatosis--a case of brain MRI abnormality and osteoporosis].

M. Nakagawa, M. Osame, M. Kuriyama, 1992, Rinsho shinkeigaku = Clinical neurology.

Osteoporosis and increased bone fractures in cerebrotendinous xanthomatosis.

M. Nakagawa, M. Osame, M. Kuriyama, 1993, Metabolism: clinical and experimental.

Rapid disease progression correlates with instability of mutant SOD1 in familial ALS

M Nakagawa, A Shimizu, S Sakoda, 2005, Neurology.

Marchiafava-Bignami disease with hyperintensity on late diffusion-weighted imaging

Kei Yamada, M. Nakagawa, T. Mizuno, 2014, Acta radiologica short reports.

A case of cerebral embolism induced by serious cardiac failure after repeated administration of trastuzumab and epirubicin

M. Nakagawa, H. Ujiié, A. Teramoto, 2017 .

[Neuronal intranuclear inclusion disease in a patient who exhibited abnormal behavior].

M. Nakagawa, T. Mizuno, T. Koizumi, 2022, Rinsho shinkeigaku = Clinical neurology.

Clinical characteristics and treatment responses in new-onset epilepsy in the elderly

S. Tsuji, T. Toyota, M. Nakagawa, 2013, Seizure.

Serum albumin to globulin ratio is related to cognitive decline via reflection of homeostasis: a nested case-control study

N. Kuriyama, T. Tokuda, Kei Yamada, 2016, BMC Neurology.

cAMP‐dependent regulation of spinesin/TMPRSS5 gene expression in astrocytes

Masaki Tanaka, Yoshihisa Watanabe, N. Yamaguchi, 2008, Journal of neuroscience research.

Modeling Drug‐Induced Neuropathy Using Human iPSCs for Predictive Toxicology

M. Nakagawa, H. Inoue, T. Mizuno, 2017, Clinical pharmacology and therapeutics.

Clinical correlation of mitochondrial DNA heteroplasmy and Leber's hereditary optic neuropathy.

M. Nakagawa, Y. Isashiki, 1991, Japanese journal of ophthalmology.

[Constructive disturbance and low-level perfusion in parietal areas in amyotrophic lateral sclerosis with dementia].

M. Nakagawa, T. Mizuno, T. Ohmichi, 2015, Rinsho shinkeigaku = Clinical neurology.

A single blind randomized controlled clinical trial of mexiletine in amyotrophic lateral sclerosis: Efficacy and safety of sodium channel blocker phase II trial

Toshio Shimizu, M. Nakagawa, S. Kuwabara, 2015, Amyotrophic lateral sclerosis & frontotemporal degeneration.

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.

Cardiomyopathy in a Japanese family with the Glu61Lys transthyretin variant: a new phenotype

T. Tokuda, K. Shiga, M. Nakagawa, 2009, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Electron microscopic abnormalities of skeletal muscle in patients with collagen VI deficiency in Ullrich's disease

I. Maruyama, K. Arimura, M. Nakagawa, 2002, Acta Neuropathologica.

Concomitant alpha‐synuclein pathology in an autopsy case of amyotrophic lateral sclerosis presenting with orthostatic hypotension and cardiac arrests

K. Shiga, M. Nakagawa, T. Mizuno, 2014, Neuropathology : official journal of the Japanese Society of Neuropathology.

Early-onset parkinsonism in a pedigree with phosphoglycerate kinase deficiency and a heterozygous carrier: do PGK-1 mutations contribute to vulnerability to parkinsonism?

T. Tokuda, T. Imamura, H. Hosoi, 2017, Journal of the Neurological Sciences.

Morphologic findings in biopsied skeletal muscle and cultured fibroblasts from a female patient with Danon's disease (lysosomal glycogen storage disease without acid maltase deficiency)

M. Nakagawa, M. Osame, I. Higuchi, 1994, Journal of the Neurological Sciences.

Glial fibrillary acidic protein mutations in adult‐onset Alexander disease: clinical features observed in 12 Japanese patients

Y. Hayashi, M. Nakagawa, I. Mizuta, 2011, Acta neurologica Scandinavica.

Novel GFAP mutation in patient with adult‐onset Alexander disease presenting with spastic ataxia

Tomokatsu Yoshida, M. Nakagawa, M. Nishizawa, 2009, Movement disorders : official journal of the Movement Disorder Society.

Self-remitting and reversible parkinsonism associated with neuro-Sweet disease.

T. Tokuda, M. Kimura, M. Nakagawa, 2010, Internal medicine.

Characteristics of cerebral lesions in adult-onset Alexander disease

Tomokatsu Yoshida, M. Nakagawa, I. Mizuta, 2019, Neurological Sciences.

A novel three-base duplication, E243dup, of GFAP identified in a patient with Alexander disease

Tomokatsu Yoshida, M. Nakagawa, I. Mizuta, 2017, Human Genome Variation.

Quantitative Evaluation of Brain Stem Atrophy Using Magnetic Resonance Imaging in Adult Patients with Alexander Disease

Tomokatsu Yoshida, M. Nakagawa, I. Mizuta, 2017, European Neurology.

Characteristic abnormal signals in medulla oblongata-"eye spot" sign: Four cases of elderly-onset Alexander disease.

Tomokatsu Yoshida, M. Nakagawa, I. Mizuta, 2015, Neurology. Clinical practice.

Cerebral white matter damage in frontotemporal dementia assessed by diffusion tensor tractography

Masanori Nakagawa, Kei Yamada, Satoru Mori, 2008, Neuroradiology.

Characteristic Posterior-dominant Lower Limb Muscle Involvement in Limb-girdle Muscular Dystrophy due to a DNAJB6 Phe93Leu Mutation

K. Shiga, M. Nakagawa, I. Mizuta, 2017, Internal medicine.

Evaluation of usefulness of anti-HTLV-I antibody titer measurement in the spinal fluid for establishing diagnosis of HAM/TSP

M. Nakagawa, M. Osame, K. Usuku, 1999 .

[Clinical aspects of mitochondrial encephalomyopathy--abnormality of mitochondrial respiratory chain].

M. Nakagawa, M. Osame, 1990, No to shinkei = Brain and nerve.

Effectiveness of Daily Prednisolone to Slow Progression of Human T-Lymphotropic Virus Type 1-Associated Myelopathy/Tropical Spastic Paraparesis: A Multicenter Retrospective Cohort Study

E. Inoue, N. Araya, M. Nakagawa, 2017, Neurotherapeutics.

A muscle ultrasound score in the diagnosis of amyotrophic lateral sclerosis

K. Shiga, M. Nakagawa, T. Mizuno, 2017, Clinical Neurophysiology.

A 10-year longitudinal study of deep white matter lesions on magnetic resonance imaging

N. Kuriyama, Kei Yamada, E. Ozaki, 2021, Neuroradiology.

Molecular pathological comparison of primary gastric B-celllymphomas in China and Japan: Polymerase chain reaction (PCR) analysis of immunoglobulin heavy chain gene variable region and direct sequencing of the product

M. Nakagawa, E. Sato, K. Hasui, 1999 .

International academic project analyzing pathogenic factors in Chinese gastric B-cell lymphomas

M. Nakagawa, E. Sato, K. Hasui, 1999 .

Awaji ALS criteria increase the diagnostic sensitivity in patients with bulbar onset

M. Nakagawa, S. Kuwabara, K. Kanai, 2012, Clinical Neurophysiology.

Creation and validation of a bladder dysfunction symptom score for HTLV-1-associated myelopathy/tropical spastic paraparesis

J. Kira, H. Yonezawa, Takahiko Ueno, 2020, Orphanet Journal of Rare Diseases.

Response of striosomal opioid signaling to dopamine depletion in 6-hydroxydopamine-lesioned rat model of Parkinson's disease: a potential compensatory role

R. Kaji, M. Nakagawa, S. Goto, 2013, Front. Cell. Neurosci..

Oral Cnm-positive Streptococcus Mutans Expressing Collagen Binding Activity is a Risk Factor for Cerebral Microbleeds and Cognitive Impairment

N. Kuriyama, R. Friedland, Kei Yamada, 2016, Scientific Reports.

Low vitamin and carotenoid levels are related to cerebral white matter lesions

N. Kuriyama, Y. Nagakane, M. Nakagawa, 2012, The journal of nutrition, health & aging.

Effect of thin-section diffusion-weighted MR imaging on stroke diagnosis.

K. Yoshikawa, Kei Yamada, T. Nishimura, 2005, AJNR. American journal of neuroradiology.

[Muscle type acid maltase deficiency. An intermediate case between childhood type and adult type (author's transl)].

M. Nakagawa, M. Osame, O. Nakazato, 1982, Rinshō shinkeigaku Clinical neurology.

Association between α-Klotho and Deep White Matter Lesions in the Brain: A Pilot Case Control Study Using Brain MRI.

N. Kuriyama, Kei Yamada, T. Koyama, 2017, Journal of Alzheimer's disease : JAD.

Ultra-high-dose methylcobalamin in amyotrophic lateral sclerosis: a long-term phase II/III randomised controlled study

Y. Ohashi, K. Okamoto, R. Kaji, 2019, Journal of Neurology, Neurosurgery, and Psychiatry.

Usefulness of serum S100B as a marker for the acute phase of aquaporin-4 autoimmune syndrome

T. Tokuda, M. Nakagawa, T. Mizuno, 2011, Neuroscience Letters.

Discrepancy between clinical and pathological diagnoses of CBD and PSP

Y. Takanashi, K. Shiga, M. Nakagawa, 2005, Journal of Neurology.

[A Case of Neuromyelitis Optica with Relapse Symptoms from Paroxysmal Pruritus].

Tomokatsu Yoshida, M. Nakagawa, T. Mizuno, 2015, Brain and nerve = Shinkei kenkyu no shinpo.

Radiological and Laboratory Features of Multiple Sclerosis Patients With Immunosuppressive Therapy: A Multicenter Retrospective Study in Japan

R. Takahashi, M. Nakagawa, T. Mizuno, 2021, Frontiers in Neurology.

Detection of early neuronal damage in CADASIL patients by q-space MR imaging

Masanori Nakagawa, Naozo Sugimoto, Kei Yamada, 2013, Neuroradiology.

Prominent fatigue in spinal muscular atrophy and spinal and bulbar muscular atrophy: Evidence of activity-dependent conduction block

M. Nakagawa, M. Mori, S. Kuwabara, 2013, Clinical Neurophysiology.

Microbleeds in Alzheimer Disease Are More Related to Cerebral Amyloid Angiopathy than Cerebrovascular Disease

Masanori Nakagawa, Kei Yamada, Satoru Mori, 2006, Dementia and Geriatric Cognitive Disorders.

Molecular genetic analysis of dysferlin in Japanese patients with Miyoshi myopathy

I. Nonaka, Y. Hayashi, M. Nakagawa, 1999 .

Increased levels of plasma total tau in adult Down syndrome

T. Tokuda, D. Allsop, M. Nakagawa, 2017, PloS one.

Somatotopic organization of thalamocortical projection fibers as assessed with MR tractography.

Masanori Nakagawa, Kei Yamada, Hirotoshi Ito, 2007, Radiology.

The functional analysis of TDP-43 by Drosophila ALS model

Masanori Nakagawa, Yukie Okada, Takahiko Tokuda, 2016 .

Axotomy induces axonogenesis in hippocampal neurons through STAT3

T. Yamashita, M. Nakagawa, Y. Fujita, 2011, Cell Death and Disease.

Characteristic expression of p57/Kip2 in balloon cells in focal cortical dysplasia

H. Kitaura, A. Kakita, S. Kameyama, 2015, Neuropathology (Kyoto. 1993).

Intravenous immunoglobulin improved cognitive functions in patients with Alzheimer's disease without any changes in PIB retention in the brain

T. Tokuda, M. Nakagawa, H. Mori, 2011, Alzheimer's & Dementia.

Chronic inflammatory demyelinating polyneuropathy due to the administration of pegylated interferon α-2b: a neuropathology case report.

K. Shiga, M. Nakagawa, T. Mizuno, 2012, Internal medicine.

Clinical investigation of the lesions responsible for sensory disturbance in Minamata disease.

K. Arimura, M. Nakagawa, Y. Ando, 2001, The Tohoku journal of experimental medicine.

Regional Cerebral Blood Flow in [123]I-IMP Single-photon Emission Computed Tomography and the Wechsler Memory Scale-revised in Nondemented Elderly Subjects with Subjective Cognitive Impairment

J. Imanishi, M. Nakagawa, T. Mizuno, 2016, Internal medicine.

Biochemical studies in mitochondrial encephalomyopathy.

S. Dimauro, H. Reichmann, Y. Kuroiwa, 1987, Journal of neurology, neurosurgery, and psychiatry.

MR perfusion imaging for stroke

Kei Yamada, K. Mineura, Y. Nagakane, 2010 .

Diffusion tensor imaging may help the determination of time at onset in cerebral ischaemia

Y. Nagakane, M. Nakagawa, K. Yamada, 2009, Journal of Neurology, Neurosurgery & Psychiatry.

Ventricular Temperatures in Idiopathic Normal Pressure Hydrocephalus (iNPH) Measured with DWI-based MR Thermometry.

N. Kuriyama, T. Tokuda, Kei Yamada, 2015, Magnetic resonance in medical sciences : MRMS : an official journal of Japan Society of Magnetic Resonance in Medicine.

Prediction Model of Amyotrophic Lateral Sclerosis by Deep Learning with Patient Induced Pluripotent Stem Cells

M. Morita, R. Takahashi, M. Nakagawa, 2021, Annals of Neurology.

Activity-dependent changes in impulse conduction of single human motor axons: A stimulated single fiber electromyography study

M. Nakagawa, S. Kuwabara, K. Kanai, 2011, Clinical Neurophysiology.

A Case of Refractory Generalized Myasthenia Gravis Treated with Polypharmacy and Plasma Exchange

M. Nakagawa, T. Mizuno, T. Hatta, 2016 .

Autonomic nervous evaluation in the early stages of olivopontocerebellar atrophy

Masanori Nakagawa, Yoshiyuki Watanabe, Toshiki Mizuno, 2005, Autonomic Neuroscience.

Brain tissue perfusion monitoring using Sonopod for transcranial color duplex sonography

K. Yoshikawa, M. Nakagawa, T. Mizuno, 2012 .

Monitoring of brain tissue perfusion utilizing a transducer holder for transcranial color duplex sonography.

K. Yoshikawa, M. Nakagawa, T. Shiogai, 2013, Acta neurochirurgica. Supplement.

Correlation of Aβ oligomer levels in matched cerebrospinal fluid and serum samples

T. Tokuda, D. Allsop, M. Taylor, 2013, Neuroscience Letters.

Recent studies on the epidemiology, clinical features and pathogenic mechanisms of HTLV-I associated myelopathy (HAM/TSP) and other diseases associated to HTLV.

K. Arimura, M. Nakagawa, S. Izumo, 1997, Journal of neurovirology.

Familial skeletal myopathy with atrioventricular block.

M. Nakagawa, M. Osame, I. Higuchi, 1999, Internal medicine.

Behçet's disease and Sjögren syndrome in a patient with HTLV-I-associated myelopathy

M. Nakagawa, M. Osame, I. Higuchi, 1993, Journal of the Neurological Sciences.

P603: Contrasting echogenicity in FDP-FCU: a diagnostic ultrasound pattern in sporadic inclusion body myositis

K. Shiga, M. Nakagawa, T. Mizuno, 2014, Clinical Neurophysiology.

TGF-beta1 is associated with the progression of intracranial deep white matter lesions: a pilot study with 5 years of magnetic resonance imaging follow-up

N. Kuriyama, Kei Yamada, Y. Nagakane, 2014, Neurological research.

Lyme disease acquired outside of Japan.

M. Nakagawa, M. Osame, K. Matsumuro, 1992, Internal medicine.

Concomitant alpha‐synuclein pathology in an autopsy case of amyotrophic lateral sclerosis presenting with orthostatic hypotension and cardiac arrests

K. Shiga, M. Nakagawa, T. Mizuno, 2014, Neuropathology : official journal of the Japanese Society of Neuropathology.

Month of birth in multiple sclerosis with and without longitudinally extensive spinal cord lesions: A study of a Japanese national survey

J. Kira, M. Kinoshita, M. Nakagawa, 2013, Journal of the Neurological Sciences.

Ventricular Temperatures in Idiopathic Normal Pressure Hydrocephalus (iNPH) Measured with DWI-based MR Thermometry.

N. Kuriyama, T. Tokuda, Kei Yamada, 2015, Magnetic resonance in medical sciences : MRMS : an official journal of Japan Society of Magnetic Resonance in Medicine.

Retrograde jugular flow associated with idiopathic normal pressure hydrocephalus

N. Kuriyama, T. Tokuda, M. Nakagawa, 2008, Annals of neurology.

Effects of peripheral lymphocyte subpopulations and the clinical correlation with Parkinson's disease

N. Kuriyama, J. Imanishi, M. Nakagawa, 2012, Geriatrics & gerontology international.

Diagnostic Value of Muscle [11C] PIB-PET in Inclusion Body Myositis

T. Tokuda, M. Nakagawa, T. Mizuno, 2020, Frontiers in Neurology.

[A rare complication of dysarthria in a patient with inclusion body myositis: a case report].

T. Tokuda, K. Shiga, M. Nakagawa, 2010, Rinsho shinkeigaku = Clinical neurology.

Safety and efficacy of interferon-α in 167 patients with human T-cell lymphotropic virus type 1-associated myelopathy

Y. Itoyama, J. Kira, K. Arimura, 2007, Journal of NeuroVirology.

[A case of amyotrophic lateral sclerosis presenting as motor aphasia in its early stage].

Y. Nagakane, M. Nakagawa, M. Muranishi, 2006, No to shinkei = Brain and nerve.