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Expanded clinical spectrum of oculopharyngodistal myopathy type 1

Muscle & nerve, 2022-12, Vol.66 (6), p.679-685

2022

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Reduced impact of viral load of HHV-6 in liquor on severity of AESD due to exanthema subitum: A case report and literature review

Brain & development (Tokyo. 1979), 2021-09, Vol.43 (8), p.879-883

2021

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Identification and segmentation of myelinated nerve fibers in a cross-sectional optical microscopic image using a deep learning model

Journal of neuroscience methods, 2017-11, Vol.291, p.141-149

2017

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Immunotherapy for ocular myasthenia gravis: an observational study in Japan

Therapeutic advances in neurological disorders, 2023-01, Vol.16, p.17562864231163819-17562864231163819

2023

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Low back pain due to superior cluneal nerve entrapment: A clinicopathologic study

Muscle & nerve, 2018-05, Vol.57 (5), p.777-783

2018

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Restoration of spatial memory dysfunction of human APP transgenic mice by transplantation of neuronal precursors derived from human iPS cells

Neuroscience letters, 2013-12, Vol.557, p.129-134

2013

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Alanine transaminase is predominantly increased in the active phase of anti-HMGCR myopathy

Neuromuscular disorders : NMD, 2022-01, Vol.32 (1), p.25-32

2022

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Roles of Reelin/Disabled1 pathway on functional recovery of hemiplegic mice after neural cell transplantation; Reelin promotes migration toward motor cortex and maturation to motoneurons of neural grafts

Experimental neurology, 2019-10, Vol.320, p.112970-112970, Article 112970

2019

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Cellular and molecular mechanisms of the restoration of human APP transgenic mouse cognitive dysfunction after transplant of human iPS cell-derived neural cells

Experimental neurology, 2015-09, Vol.271, p.423-431

2015

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Long-term outcomes in motor and cognitive impairment with acute encephalopathy

Brain & development (Tokyo. 1979), 2018-10, Vol.40 (9), p.807-812

2018

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Slowly progressive D-bifunctional protein deficiency with survival to adulthood diagnosed by whole-exome sequencing

Journal of the neurological sciences, 2017-01, Vol.372, p.6-10

2017

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Needle electromyography, muscle MRI, and muscle pathology: Correlations in idiopathic inflammatory myopathies

Neurology and clinical neuroscience, 2020-01, Vol.8 (1), p.28-35

2020

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Severe dilated cardiomyopathy and ventricular arrhythmia in a patient with Emery‐Dreifuss muscular dystrophy harboring a novel frameshift mutation in EMD

Neurology and clinical neuroscience, 2021-11, Vol.9 (6), p.490-493

2021

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Apoptosis of primary sensory neurons in GD1b-induced sensory ataxic neuropathy

Experimental neurology, 2008-01, Vol.209 (1), p.279-283

2008

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“Localized” chronic invasive fungal rhinosinusitis without serological abnormalities

Neurology and clinical neuroscience, 2019-03, Vol.7 (2), p.96-97

2019

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Spontaneous Regression of an Asymptomatic Meningioma Associated With Discontinuation of Progesterone Agonist Administration: Case Report

Neurologia medico-chirurgica, 2008, Vol.48(5), pp.227-230

2008

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Treatment consensus for management of polymyositis and dermatomyositis among rheumatologists, neurologists and dermatologists

Neurology and clinical neuroscience, 2019-01, Vol.7 (1), p.3-21

2019

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Familial amyloid polyneuropathy diagnosed by minor salivary gland biopsy

Neurology and clinical neuroscience, 2018-03, Vol.6 (2), p.67-67

2018

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A case of late‐onset Leber's hereditary optic neuropathy with elevated serum lactic acid and pyruvic acid levels by cycle ergometer exercise

Neurology and clinical neuroscience, 2018-11, Vol.6 (6), p.179-181

2018

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A case of late‐onset Krabbe disease which showed subacute progression of spastic paresis with bilateral spinal cord lesions

Neurology and clinical neuroscience, 2018-07, Vol.6 (4), p.104-106

2018

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Unilaterally and rapidly progressing white matter lesion and elevated cytokines in a patient with Tay–Sachs disease

Brain & development (Tokyo. 1979), 2010-03, Vol.32 (3), p.244-247

2010

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Neuronal intranuclear inclusion disease presenting with recurrent cerebral infarct‐like lesions

Neurology and clinical neuroscience, 2015-09, Vol.3 (5), p.185-187

2015

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Novel COL6A2 mutation in a case of limb girdle muscular dystrophy phenotype with autosomal recessive inheritance

Neurology and clinical neuroscience, 2016-09, Vol.4 (5), p.189-191

2016

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A clinicopathological study of low back pain due to middle cluneal nerve entrapment: case series

European spine journal, 2024-02, Vol.33 (2), p.490-495

2024

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An Aneurysm Rupturing into a Middle Cranial Fossa Arachnoid Cyst Presenting as an Intracystic Hemorrhage

Journal of stroke and cerebrovascular diseases, 2012-04, Vol.21 (3), p.243-244

2012

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Expanded clinical spectrum of oculopharyngodistal myopathy type 1

Reduced impact of viral load of HHV-6 in liquor on severity of AESD due to exanthema subitum: A case report and literature review

Identification and segmentation of myelinated nerve fibers in a cross-sectional optical microscopic image using a deep learning model

Immunotherapy for ocular myasthenia gravis: an observational study in Japan

Low back pain due to superior cluneal nerve entrapment: A clinicopathologic study

Restoration of spatial memory dysfunction of human APP transgenic mice by transplantation of neuronal precursors derived from human iPS cells

Alanine transaminase is predominantly increased in the active phase of anti-HMGCR myopathy

Roles of Reelin/Disabled1 pathway on functional recovery of hemiplegic mice after neural cell transplantation; Reelin promotes migration toward motor cortex and maturation to motoneurons of neural grafts

Cellular and molecular mechanisms of the restoration of human APP transgenic mouse cognitive dysfunction after transplant of human iPS cell-derived neural cells

Long-term outcomes in motor and cognitive impairment with acute encephalopathy

Slowly progressive D-bifunctional protein deficiency with survival to adulthood diagnosed by whole-exome sequencing

Needle electromyography, muscle MRI, and muscle pathology: Correlations in idiopathic inflammatory myopathies

Severe dilated cardiomyopathy and ventricular arrhythmia in a patient with Emery‐Dreifuss muscular dystrophy harboring a novel frameshift mutation in EMD

Apoptosis of primary sensory neurons in GD1b-induced sensory ataxic neuropathy

“Localized” chronic invasive fungal rhinosinusitis without serological abnormalities

Spontaneous Regression of an Asymptomatic Meningioma Associated With Discontinuation of Progesterone Agonist Administration: Case Report

Treatment consensus for management of polymyositis and dermatomyositis among rheumatologists, neurologists and dermatologists

Familial amyloid polyneuropathy diagnosed by minor salivary gland biopsy

A case of late‐onset Leber's hereditary optic neuropathy with elevated serum lactic acid and pyruvic acid levels by cycle ergometer exercise

A case of late‐onset Krabbe disease which showed subacute progression of spastic paresis with bilateral spinal cord lesions

Unilaterally and rapidly progressing white matter lesion and elevated cytokines in a patient with Tay–Sachs disease

Neuronal intranuclear inclusion disease presenting with recurrent cerebral infarct‐like lesions

Novel COL6A2 mutation in a case of limb girdle muscular dystrophy phenotype with autosomal recessive inheritance

A clinicopathological study of low back pain due to middle cluneal nerve entrapment: case series

An Aneurysm Rupturing into a Middle Cranial Fossa Arachnoid Cyst Presenting as an Intracystic Hemorrhage

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