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Atypical Familial Amyotrophic Lateral Sclerosis with Slowly Progressing Lower Extremities-predominant Late-onset Muscular Weakness and Atrophy

Internal Medicine, 2019/07/01, Vol.58(13), pp.1851-1858

2019

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A case of cerebellar ataxia associated with VZV infection

eNeurologicalSci, 2018-06, Vol.11, p.9-10

2018

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A case of idiopathic propriospinal myoclonus accompanied by giant somatosensory evoked potential

Rinshō shinkeigaku, 2022, Vol.62 (11), p.865-868, Article cn-001737

2022

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Brachial Plexus Neurolymphomatosis:A Discrepancy between Electrophysiological and Radiological Findings

Internal Medicine, 2007, Vol.46(8), pp.533-534

2007

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Eyes and hands oscillation in HIV-associated neurocognitive disorder: A case report

Journal of the neurological sciences, 2019-09, Vol.404, p.112-114

2019

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GCH1 mutations in dopa-responsive dystonia and Parkinson’s disease

Journal of neurology, 2018-08, Vol.265 (8), p.1860-1870

2018

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Confirmation of the efficacy of vitamin B 6 supplementation for McArdle disease by follow‐up muscle biopsy

Muscle & nerve, 2012-03, Vol.45 (3), p.436-440

2012

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Development of Severe Longitudinal Atrophy of Thoracic Spinal Cord Following Lupus-Related Myelitis

Internal Medicine, 2001, Vol.40(4), pp.353-357

2001

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Selective impairment and a unique recovery of bilateral horizontal gaze and facial palsy in a discrete pontine lesion: a case report

Rinshō shinkeigaku, 2011, Vol.51 (2), p.125-129

2011

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Bilateral Optic Neuropathy with Bilateral Putaminal Lesions: A Case Report

Journal of Neuroimaging, 2015, Vol.25 (3), p.514-516

2015

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Simple and defined method to detect the SOD-1 mutants from patients with familial amyotrophic lateral sclerosis by mass spectrometry

Journal of neuroscience methods, 1998-06, Vol.81 (1), p.41-44

1998

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Corrigendum to “Clinical features and neuropathological findings of familial amyotrophic lateral sclerosis with a His46Arg mutation in Cu/Zn superoxide dismutase” [J. Neurol. Sci. 197 (2002) 73–78]

Journal of the neurological sciences, 2002-09, Vol.201 (1), p.93-93

2002

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Level of nerve growth factor-like immunoreactivity in the lower limb muscles of muscular dystrophic mice

Biochemical and biophysical research communications, 1979-09, Vol.90 (1), p.130-134

1979

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Eyes and hands oscillation in HIV-associated neurocognitive disorder: A case report

Journal of the neurological sciences, 2019, Vol.404, p.112-114

2019

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Orthotic Treatments in the Management of Self-Mutilation in Lesch-Nyhan Syndrome

The Japanese Journal of Rehabilitation Medicine, 1997/09/18, Vol.34(9), pp.610-613

1997

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F-wave elicitable minimum nerve conduction velocity

Muscle & nerve, 1998-06, Vol.21 (6), p.828-829

1998

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Distribution of and age‐related changes in ciliary neurotrophic factor protein in rat tissues

Biochemistry and molecular biology international, 1996-11, Vol.40 (4), p.671-678

1996

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A deletion of five nucleotides in the LICAM gene in a Japanese family with X-linked hydrocephalus

Human genetics, 1996-03, Vol.97 (3), p.353-356

1996

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A deletion of five nucleotides in the L1CAM gene in a Japanese family with X-linked hydrocephalus

Human genetics, 1996-03, Vol.97 (3), p.353-356

1996

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Confirmation of the efficacy of vitamin B6 supplementation for McArdle disease by follow-up muscle biopsy

Muscle & Nerve, 2012, Vol.45 (3), p.436-440

2012

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An abnormality of facial nerve conduction velocity distribution (FNCVD) in Bell's palsy patients

No To Shinkei, 1998-04, Vol.50 (4), p.325

1998

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Increased endoneurial albumin in diabetic polyneuropathy

Neurology, 1985-12, Vol.35 (12), p.1790-1790

1985

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A case of tuberculous meningitis with marked contrast enhancement of the basal cisterns in computerized tomography

Nihon Naika Gakkai zasshi, 1988, Vol.77 (3), p.345-350

1988

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Molecular feature of the nerve growth factor in human serum

Life sciences (1973), 1980-03, Vol.26 (11), p.837-844

1980

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PS-3-12 An abnormality of facial nerve conduction velocity distribution in patients with Bell's palsy

Electroencephalography and clinical neurophysiology / electromyography and motor control, 1995-09, Vol.97 (4), p.S89-S90

1995

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Atypical Familial Amyotrophic Lateral Sclerosis with Slowly Progressing Lower Extremities-predominant Late-onset Muscular Weakness and Atrophy

A case of cerebellar ataxia associated with VZV infection

A case of idiopathic propriospinal myoclonus accompanied by giant somatosensory evoked potential

Brachial Plexus Neurolymphomatosis:A Discrepancy between Electrophysiological and Radiological Findings

Eyes and hands oscillation in HIV-associated neurocognitive disorder: A case report

GCH1 mutations in dopa-responsive dystonia and Parkinson’s disease

Confirmation of the efficacy of vitamin B 6 supplementation for McArdle disease by follow‐up muscle biopsy

Development of Severe Longitudinal Atrophy of Thoracic Spinal Cord Following Lupus-Related Myelitis

Selective impairment and a unique recovery of bilateral horizontal gaze and facial palsy in a discrete pontine lesion: a case report

Bilateral Optic Neuropathy with Bilateral Putaminal Lesions: A Case Report

Simple and defined method to detect the SOD-1 mutants from patients with familial amyotrophic lateral sclerosis by mass spectrometry

Corrigendum to “Clinical features and neuropathological findings of familial amyotrophic lateral sclerosis with a His46Arg mutation in Cu/Zn superoxide dismutase” [J. Neurol. Sci. 197 (2002) 73–78]

Level of nerve growth factor-like immunoreactivity in the lower limb muscles of muscular dystrophic mice

Eyes and hands oscillation in HIV-associated neurocognitive disorder: A case report

Orthotic Treatments in the Management of Self-Mutilation in Lesch-Nyhan Syndrome

F-wave elicitable minimum nerve conduction velocity

Distribution of and age‐related changes in ciliary neurotrophic factor protein in rat tissues

A deletion of five nucleotides in the LICAM gene in a Japanese family with X-linked hydrocephalus

A deletion of five nucleotides in the L1CAM gene in a Japanese family with X-linked hydrocephalus

Confirmation of the efficacy of vitamin B6 supplementation for McArdle disease by follow-up muscle biopsy

An abnormality of facial nerve conduction velocity distribution (FNCVD) in Bell's palsy patients

Increased endoneurial albumin in diabetic polyneuropathy

A case of tuberculous meningitis with marked contrast enhancement of the basal cisterns in computerized tomography

Molecular feature of the nerve growth factor in human serum

PS-3-12 An abnormality of facial nerve conduction velocity distribution in patients with Bell's palsy

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