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MTCL1 plays an essential role in maintaining Purkinje neuron axon initial segment

The EMBO journal, 2017-05, Vol.36 (9), p.1227-1242

2017

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Bromisoval-induced bromism with status epilepticus mimicking Wernicke's encephalopathy: report of two cases

BMC neurology, 2022-05, Vol.22 (1), p.181-181, Article 181

2022

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Acute necrotizing encephalopathy and a carnitine palmitoyltransferase 2 variant in an adult

Journal of clinical neuroscience, 2019-03, Vol.61, p.264-266

2019

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Missing genetic variations in GNE myopathy: rearrangement hotspots encompassing 5′UTR and founder allele

Journal of human genetics, 2017-02, Vol.62 (2), p.159-166

2017

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Clinical Phenotype and Segregation of Mitochondrial 3243A>G Mutation in 2 Pairs of Monozygotic Twins

JAMA neurology, 2016-08, Vol.73 (8), p.990

2016

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A Japanese Family of Spinocerebellar Ataxia Type 21: Clinical and Neuropathological Studies

Cerebellum (London, England), 2018-10, Vol.17 (5), p.525-530

2018

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

Cerebellum (London, England), 2017-04, Vol.16 (2), p.518-524

2017

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Left Upper Lung Lobectomy Is an Embolic Risk Factor for Cerebral Infarction

Journal of stroke and cerebrovascular diseases, 2017-09, Vol.26 (9), p.e177-e179

2017

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Seronegative neuromyelitis optica spectrum disorder in primary familial brain calcification with PDGFB variant

eNeurologicalSci, 2022-06, Vol.27, p.100406-100406, Article 100406

2022

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Missing genetic variations in GNE myopathy: rearrangement hotspots encompassing 5'UTR and founder allele

Journal of human genetics, 2017-02, Vol.62 (2), p.159-166

2017

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Shinshu Brain Resource Net

Neuropathology, 2016-12, Vol.36 (6), p.600-601

2016

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Increase in Incidence of Elderly-onset Patients with Myasthenia Gravis in Nagano Prefecture, Japan

Internal Medicine, 2005, Vol.44(6), pp.572-577

2005

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Cerebral amyloid angiopathy in posttransplant patients with hereditary ATTR amyloidosis

Neurology, 2016-08, Vol.87 (8), p.773-781

2016

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V-shaped MRI change in the midbrain of a patient with artery of Percheron infarction

Neurology India, 2019-05, Vol.67 (3), p.927-927

2019

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Dystonia and Parkinsonism in COA7-related disorders: expanding the phenotypic spectrum

Journal of neurology, 2024-01, Vol.271 (1), p.419-430

2024

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Shock and stony hard ears

The Lancet (British edition), 2007-03, Vol.369 (9564), p.856-856

2007

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Intravascular Large B Cell Lymphoma Diagnosed by Senile Angioma Biopsy

Internal Medicine, 2003, Vol.42(1), pp.117-120

2003

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Late changes on magnetic resonance imaging in posterior spinal artery syndrome: A report and literature review

Neurology India, 2019-03, Vol.67 (2), p.571-573

2019

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Role of Individual T-Cell Epitopes of Theiler’s Virus in the Pathogenesis of Demyelination Correlates with the Ability To Induce a Th1 Response

Journal of Virology, 1998-07, Vol.72 (7), p.6169-6174

1998

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Erythroblast appearance associated with natalizumab

Multiple sclerosis and related disorders, 2019-04, Vol.29, p.145-147

2019

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Suppressive Effect on Theiler's Murine Encephalomyelitis Virus-Induced Demyelinating Disease by the Administration of Anti-IL-12 Antibody

The Journal of immunology (1950), 1998-11, Vol.161 (10), p.5586-5593

1998

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The level of tumor necrosis factor-α producing cells in the spinal cord correlates with the degree of Theiler's murine encephalomyelitis virus-induced demyelinating disease

International immunology, 1996-07, Vol.8 (7), p.1001-1008

1996

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Predominant cerebellar phenotype in spastic paraplegia 7 (SPG7)

Human genome variation, 2015-03, Vol.2 (1), p.15012-15012, Article 15012

2015

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A case of colchicine-responsive Mollaret's meningitis with MEFV gene mutation

Rinsho shinkeigaku = Clinical neurology, 2014, Vol.54 (2), p.124

2014

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A case of colchicine-responsive Mollaret’s meningitis with MEFV gene mutation

Rinshō shinkeigaku, 2014, Vol.54 (2), p.124-129

2014

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MTCL1 plays an essential role in maintaining Purkinje neuron axon initial segment

Bromisoval-induced bromism with status epilepticus mimicking Wernicke's encephalopathy: report of two cases

Acute necrotizing encephalopathy and a carnitine palmitoyltransferase 2 variant in an adult

Missing genetic variations in GNE myopathy: rearrangement hotspots encompassing 5′UTR and founder allele

Clinical Phenotype and Segregation of Mitochondrial 3243A>G Mutation in 2 Pairs of Monozygotic Twins

A Japanese Family of Spinocerebellar Ataxia Type 21: Clinical and Neuropathological Studies

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

Left Upper Lung Lobectomy Is an Embolic Risk Factor for Cerebral Infarction

Seronegative neuromyelitis optica spectrum disorder in primary familial brain calcification with PDGFB variant

Missing genetic variations in GNE myopathy: rearrangement hotspots encompassing 5'UTR and founder allele

Shinshu Brain Resource Net

Increase in Incidence of Elderly-onset Patients with Myasthenia Gravis in Nagano Prefecture, Japan

Cerebral amyloid angiopathy in posttransplant patients with hereditary ATTR amyloidosis

V-shaped MRI change in the midbrain of a patient with artery of Percheron infarction

Dystonia and Parkinsonism in COA7-related disorders: expanding the phenotypic spectrum

Shock and stony hard ears

Intravascular Large B Cell Lymphoma Diagnosed by Senile Angioma Biopsy

Late changes on magnetic resonance imaging in posterior spinal artery syndrome: A report and literature review

Role of Individual T-Cell Epitopes of Theiler’s Virus in the Pathogenesis of Demyelination Correlates with the Ability To Induce a Th1 Response

Erythroblast appearance associated with natalizumab

Suppressive Effect on Theiler's Murine Encephalomyelitis Virus-Induced Demyelinating Disease by the Administration of Anti-IL-12 Antibody

The level of tumor necrosis factor-α producing cells in the spinal cord correlates with the degree of Theiler's murine encephalomyelitis virus-induced demyelinating disease

Predominant cerebellar phenotype in spastic paraplegia 7 (SPG7)

A case of colchicine-responsive Mollaret's meningitis with MEFV gene mutation

A case of colchicine-responsive Mollaret’s meningitis with MEFV gene mutation

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