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Long-term effects of the gait treatment using a wearable cyborg hybrid assistive limb in a patient with spinal and bulbar muscular atrophy: a case report with 5 years of follow-up

Frontiers in neurology, 2023-06, Vol.14, p.1143820

2023

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

Human genome variation, 2023-03, Vol.10 (1), p.10-10, Article 10

2023

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A Cross-Sectional Study on Socioeconomic Systems Supporting Outpatients With Parkinson's Disease in Japan

Journal of epidemiology, 2016, Vol.26 (4), p.185-190

2016

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Effect of 1,25-dihydroxyvitamin D3 on cultured mesencephalic dopaminergic neurons to the combined toxicity caused by L-buthionine sulfoximine and 1-methyl-4-phenylpyridine

Journal of neuroscience research, 2000-11, Vol.62 (3), p.374-382

2000

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Neurotoxicity of methylglyoxal and 3-deoxyglucosone on cultured cortical neurons: Synergism between glycation and oxidative stress, possibly involved in neurodegenerative diseases

Journal of neuroscience research, 1999-07, Vol.57 (2), p.280-289

1999

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

Stroke (1970), 2014-05, Vol.45 (5), p.1415-1421

2014

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Differentiation of speech in Parkinson’s disease and spinocerebellar degeneration using deep neural networks

Journal of neurology, 2024-02, Vol.271 (2), p.1004-1012

2024

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Executive dysfunction in patients with spinocerebellar ataxia type 3

Journal of neurology, 2018-07, Vol.265 (7), p.1563-1572

2018

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Overlap of acute mydriasis and acute pharyngeal weakness associated with anti‐GQ1b antibodies

Muscle & nerve, 2018-01, Vol.57 (1), p.E94-E95

2018

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Prospective 10-year surveillance of human prion diseases in Japan

Brain (London, England : 1878), 2010-10, Vol.133 (10), p.3043-3057

2010

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Cognitive dysfunction in patients with spinocerebellar ataxia type 6

Journal of neurology, 2017-02, Vol.264 (2), p.260-267

2017

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Significance of the Hemorrhagic Site for Recurrent Bleeding: Prespecified Analysis in the Japan Adult Moyamoya Trial

Stroke (1970), 2016-01, Vol.47 (1), p.37-43

2016

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A case of pure autotopagnosia following Creutzfeldt-Jakob disease

Cognitive neuropsychology, 2016-10, Vol.33 (7-8), p.398-404

2016

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Protective effects of the TNF-ceramide pathway against glutamate neurotoxicity on cultured mesencephalic neurons

Brain research, 1999-02, Vol.819 (1), p.170-173

1999

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

Journal of the neurological sciences, 2017-01, Vol.372, p.444-446

2017

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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

Journal of the neurological sciences, 2017-04, Vol.375, p.490-491

2017

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

Journal of neurology, 2000-06, Vol.247 (6), p.474-475

2000

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Analysis of resources assisting in coping with swallowing difficulties for patients with Parkinson's disease: a cross-sectional study

BMC health services research, 2016-07, Vol.16 (1), p.276-276, Article 276

2016

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Neurotoxicity of Methylglyoxal and 3-Deoxyglucosone on Cultured Cortical Neurons: Synergism Between Glycation and Oxidative Stress, Possibly Involved in Neurodegenerative Diseases

Journal of neuroscience research, 1999-07, Vol.57 (2), p.280-289

1999

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Autosomal dominant spastic paraplegia linked to chromosome 2p: clinical and genetic studies of a large Japanese pedigree

Journal of the neurological sciences, 1997-10, Vol.151 (1), p.65-70

1997

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Temporal Alterations of Immunohistochemical Findings in Polymyositis

Internal Medicine, 1994, Vol.33(5), pp.263-270

1994

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Prevalence of Parkinson's Disease in Hokkaido, the Northernmost Island of Japan

Internal Medicine, 1996, Vol.35(4), pp.276-279

1996

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Selective vulnerability of spinal motor neurons to reactive dicarbonyl compounds, intermediate products of glycation, in vitro: implication of inefficient glutathione system in spinal motor neurons

Brain research, 2000-04, Vol.861 (1), p.151-159

2000

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Infiltrating Cell Profiles of Sarcoid Lesions in the Muscles and Peripheral Nerves: an Immunohistological Study

Internal Medicine, 1997, Vol.36(12), pp.876-881

1997

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O4‐03‐05: Human prion diseases in Japan: analysis of 1,552 patients in a prospective 11‐year surveillance

Alzheimer's & dementia, 2011-07, Vol.7 (4S_Part_20), p.S687-S687

2011

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Long-term effects of the gait treatment using a wearable cyborg hybrid assistive limb in a patient with spinal and bulbar muscular atrophy: a case report with 5 years of follow-up

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

A Cross-Sectional Study on Socioeconomic Systems Supporting Outpatients With Parkinson's Disease in Japan

Effect of 1,25-dihydroxyvitamin D3 on cultured mesencephalic dopaminergic neurons to the combined toxicity caused by L-buthionine sulfoximine and 1-methyl-4-phenylpyridine

Neurotoxicity of methylglyoxal and 3-deoxyglucosone on cultured cortical neurons: Synergism between glycation and oxidative stress, possibly involved in neurodegenerative diseases

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

Differentiation of speech in Parkinson’s disease and spinocerebellar degeneration using deep neural networks

Executive dysfunction in patients with spinocerebellar ataxia type 3

Overlap of acute mydriasis and acute pharyngeal weakness associated with anti‐GQ1b antibodies

Prospective 10-year surveillance of human prion diseases in Japan

Cognitive dysfunction in patients with spinocerebellar ataxia type 6

Significance of the Hemorrhagic Site for Recurrent Bleeding: Prespecified Analysis in the Japan Adult Moyamoya Trial

A case of pure autotopagnosia following Creutzfeldt-Jakob disease

Protective effects of the TNF-ceramide pathway against glutamate neurotoxicity on cultured mesencephalic neurons

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

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

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

Analysis of resources assisting in coping with swallowing difficulties for patients with Parkinson's disease: a cross-sectional study

Neurotoxicity of Methylglyoxal and 3-Deoxyglucosone on Cultured Cortical Neurons: Synergism Between Glycation and Oxidative Stress, Possibly Involved in Neurodegenerative Diseases

Autosomal dominant spastic paraplegia linked to chromosome 2p: clinical and genetic studies of a large Japanese pedigree

Temporal Alterations of Immunohistochemical Findings in Polymyositis

Prevalence of Parkinson's Disease in Hokkaido, the Northernmost Island of Japan

Selective vulnerability of spinal motor neurons to reactive dicarbonyl compounds, intermediate products of glycation, in vitro: implication of inefficient glutathione system in spinal motor neurons

Infiltrating Cell Profiles of Sarcoid Lesions in the Muscles and Peripheral Nerves: an Immunohistological Study

O4‐03‐05: Human prion diseases in Japan: analysis of 1,552 patients in a prospective 11‐year surveillance

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