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Neuropathic pain correlates with myelinated fibre loss and cytokine profile in POEMS syndrome

Journal of neurology, neurosurgery and psychiatry, 2008-10, Vol.79 (10), p.1171-1179

2008

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Pathogenesis and molecular targeted therapy of spinal and bulbar muscular atrophy

Neuropathology and applied neurobiology, 2007-04, Vol.33 (2), p.135-151

2007

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Cardiac (123)I-meta-iodobenzylguanidine (MIBG) uptake in dementia with Lewy bodies: comparison with Alzheimer's disease

Journal of neurology, neurosurgery and psychiatry, 2001-06, Vol.70 (6), p.781-783

2001

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Neuropsychological backgrounds of the patients with botulinum toxin ineffective spasmodic torticollis

Journal of the neurological sciences, 2017-10, Vol.381, p.1051-1051

2017

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Spect findings in Parkinson’s disease – 2nd report: Relevance to hallucinations induced by antiparkinsonian drugs

Journal of the neurological sciences, 2019-10, Vol.405, p.190-190

2019

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17-AAG, an Hsp90 inhibitor, ameliorates polyglutamine-mediated motor neuron degeneration

Nature medicine, 2005-10, Vol.11 (10), p.1088-1095

2005

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Pharmacological Induction of Heat-Shock Proteins Alleviates Polyglutamine-Mediated Motor Neuron Disease

Proceedings of the National Academy of Sciences - PNAS, 2005-11, Vol.102 (46), p.16801-16806

2005

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Molecular features of the CAG repeats and clinical manifestation of Machado-Joseph disease

Human molecular genetics, 1995-05, Vol.4 (5), p.807-812

1995

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Testosterone Reduction Prevents Phenotypic Expression in a Transgenic Mouse Model of Spinal and Bulbar Muscular Atrophy

Neuron (Cambridge, Mass.), 2002-08, Vol.35 (5), p.843-854

2002

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Tumor necrosis factor-α expression in muscles of polymyositis and dermatomyositis

Acta neuropathologica, 2000-05, Vol.99 (5), p.585-588

2000

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Gene expression profile of spinal motor neurons in sporadic amyotrophic lateral sclerosis

Annals of neurology, 2005-02, Vol.57 (2), p.236-251

2005

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Progression and prognosis in multiple system atrophy. An analysis of 230 Japanese patients

Brain (London, England : 1878), 2002-05, Vol.125 (Pt 5), p.1070-1083

2002

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Heat Shock Protein 70 Chaperone Overexpression Ameliorates Phenotypes of the Spinal and Bulbar Muscular Atrophy Transgenic Mouse Model by Reducing Nuclear-Localized Mutant Androgen Receptor Protein

The Journal of neuroscience, 2003-03, Vol.23 (6), p.2203-2211

2003

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Pathophysiological analysis of spinal and bulbar muscular atrophy using disease-specific iPSCs

Journal of the neurological sciences, 2017-10, Vol.381, p.708-708

2017

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A Rescue Factor Abolishing Neuronal Cell Death by a Wide Spectrum of Familial Alzheimer's Disease Genes and Aβ

Proceedings of the National Academy of Sciences - PNAS, 2001-05, Vol.98 (11), p.6336-6341

2001

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Sodium butyrate ameliorates phenotypic expression in a transgenic mouse model of spinal and bulbar muscular atrophy

Human molecular genetics, 2004-06, Vol.13 (11), p.1183-1192

2004

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Leuprorelin rescues polyglutamine-dependent phenotypes in a transgenic mouse model of spinal and bulbar muscular atrophy

Nature medicine, 2003-06, Vol.9 (6), p.768-773

2003

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Differential expression of inflammation‐ and apoptosis‐related genes in spinal cords of a mutant SOD1 transgenic mouse  model of familial amyotrophic lateral sclerosis

Journal of neurochemistry, 2002-01, Vol.80 (1), p.158-167

2002

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Efficacy and safety of leuprorelin in patients with spinal and bulbar muscular atrophy (JASMITT study): a multicentre, randomised, double-blind, placebo-controlled trial

Lancet neurology, 2010-09, Vol.9 (9), p.875-884

2010

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The analysis of neuromuscular pathology of spinal-bulbar muscular atrophy using iPSC-derived disease model

Journal of the neurological sciences, 2017-10, Vol.381, p.572-572

2017

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Widespread nuclear and cytoplasmic accumulation of mutant androgen receptor in SBMA patients

Brain (London, England : 1878), 2005-03, Vol.128 (3), p.659-670

2005

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Dorfin Ubiquitylates Mutant SOD1 and Prevents Mutant SOD1-mediated Neurotoxicity

The Journal of biological chemistry, 2002-09, Vol.277 (39), p.36793-36798

2002

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Differential somatic CAG repeat instability in variable brain cell lineage in dentatorubral pallidoluysian atrophy (DRPLA): a laser-captured microdissection (LCM)-based analysis

Human genetics, 2000-11, Vol.107 (5), p.452-457

2000

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Chaperones Hsp70 and Hsp40 Suppress Aggregate Formation and Apoptosis in Cultured Neuronal Cells Expressing Truncated Androgen Receptor Protein with Expanded Polyglutamine Tract

The Journal of biological chemistry, 2000-03, Vol.275 (12), p.8772-8778

2000

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Mitochondrial Localization of Mutant Superoxide Dismutase 1 Triggers Caspase-dependent Cell Death in a Cellular Model of Familial Amyotrophic Lateral Sclerosis

The Journal of biological chemistry, 2002-12, Vol.277 (52), p.50966-50972

2002

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Neuropathic pain correlates with myelinated fibre loss and cytokine profile in POEMS syndrome

Pathogenesis and molecular targeted therapy of spinal and bulbar muscular atrophy

Cardiac (123)I-meta-iodobenzylguanidine (MIBG) uptake in dementia with Lewy bodies: comparison with Alzheimer's disease

Neuropsychological backgrounds of the patients with botulinum toxin ineffective spasmodic torticollis

Spect findings in Parkinson’s disease – 2nd report: Relevance to hallucinations induced by antiparkinsonian drugs

17-AAG, an Hsp90 inhibitor, ameliorates polyglutamine-mediated motor neuron degeneration

Pharmacological Induction of Heat-Shock Proteins Alleviates Polyglutamine-Mediated Motor Neuron Disease

Molecular features of the CAG repeats and clinical manifestation of Machado-Joseph disease

Testosterone Reduction Prevents Phenotypic Expression in a Transgenic Mouse Model of Spinal and Bulbar Muscular Atrophy

Tumor necrosis factor-α expression in muscles of polymyositis and dermatomyositis

Gene expression profile of spinal motor neurons in sporadic amyotrophic lateral sclerosis

Progression and prognosis in multiple system atrophy. An analysis of 230 Japanese patients

Heat Shock Protein 70 Chaperone Overexpression Ameliorates Phenotypes of the Spinal and Bulbar Muscular Atrophy Transgenic Mouse Model by Reducing Nuclear-Localized Mutant Androgen Receptor Protein

Pathophysiological analysis of spinal and bulbar muscular atrophy using disease-specific iPSCs

A Rescue Factor Abolishing Neuronal Cell Death by a Wide Spectrum of Familial Alzheimer's Disease Genes and Aβ

Sodium butyrate ameliorates phenotypic expression in a transgenic mouse model of spinal and bulbar muscular atrophy

Leuprorelin rescues polyglutamine-dependent phenotypes in a transgenic mouse model of spinal and bulbar muscular atrophy

Differential expression of inflammation‐ and apoptosis‐related genes in spinal cords of a mutant SOD1 transgenic mouse  model of familial amyotrophic lateral sclerosis

Efficacy and safety of leuprorelin in patients with spinal and bulbar muscular atrophy (JASMITT study): a multicentre, randomised, double-blind, placebo-controlled trial

The analysis of neuromuscular pathology of spinal-bulbar muscular atrophy using iPSC-derived disease model

Widespread nuclear and cytoplasmic accumulation of mutant androgen receptor in SBMA patients

Dorfin Ubiquitylates Mutant SOD1 and Prevents Mutant SOD1-mediated Neurotoxicity

Differential somatic CAG repeat instability in variable brain cell lineage in dentatorubral pallidoluysian atrophy (DRPLA): a laser-captured microdissection (LCM)-based analysis

Chaperones Hsp70 and Hsp40 Suppress Aggregate Formation and Apoptosis in Cultured Neuronal Cells Expressing Truncated Androgen Receptor Protein with Expanded Polyglutamine Tract

Mitochondrial Localization of Mutant Superoxide Dismutase 1 Triggers Caspase-dependent Cell Death in a Cellular Model of Familial Amyotrophic Lateral Sclerosis

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