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Axonal TDP-43 aggregates in sporadic amyotrophic lateral sclerosis

Neuropathology and applied neurobiology, 2016-10, Vol.42 (6), p.561-572

2016

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Elevated serum levels of heat-shock protein (HSP) 70 and 90 in patients with ALS

Journal of the neurological sciences, 2015-10, Vol.357, p.e340-e340

2015

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Communication support project for patients with an intractable neurological disease

Journal of the neurological sciences, 2017-10, Vol.381, p.606-606

2017

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Suspected adverse effects after human papillomavirus vaccination: a temporal relationship

Immunologic research, 2018-12, Vol.66 (6), p.723-725

2018

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The broad symptoms with genetically identified episodic ataxia type 2 in a family

Journal of the neurological sciences, 2017-10, Vol.381, p.896-896

2017

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New criteria of suspected adverse symptoms related human papillomavirus vaccination

Journal of the neurological sciences, 2017-10, Vol.381, p.850-850

2017

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Patients with ALS under tracheostomy positive-pressure ventilation (TPPV) and complicating malignant tumor

Journal of the neurological sciences, 2017-10, Vol.381, p.571-571

2017

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Clinical features and treatment outcome of four patients with anti-signal recognition particle antibody positive necrotizing myopathy

Journal of the neurological sciences, 2017-10, Vol.381, p.657-658

2017

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Mixed connective tissue disease with interstitial pneumonia in HTLV-1 carrier: case report and review of the literature

Clinical rheumatology, 2004-12, Vol.23 (6), p.548-551

2004

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Peripheral Sympathetic Nerve Dysfunction in Adolescent Japanese Girls Following Immunization with the Human Papillomavirus Vaccine

Internal Medicine, 2014, Vol.53(19), pp.2185-2200

2014

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Suspected Adverse Effects After Human Papillomavirus Vaccination: A Temporal Relationship Between Vaccine Administration and the Appearance of Symptoms in Japan

Drug safety, 2017-12, Vol.40 (12), p.1219-1229

2017

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Mutant IDH1 Dysregulates the Differentiation of Mesenchymal Stem Cells in Association with Gene-Specific Histone Modifications to Cartilage- and Bone-Related Genes

PloS one, 2015-07, Vol.10 (7), p.e0131998-e0131998

2015

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A Long-Term Observation on the Possible Adverse Effects in Japanese Adolescent Girls after Human Papillomavirus Vaccination

Vaccines (Basel), 2021-08, Vol.9 (8), p.856

2021

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Spread of vimentin‐immunoreactive cells within the plaque‐like lesion in the spinal anterior horn of a patient with post‐poliomyelitis syndrome

Neuropathology, 2021-10, Vol.41 (5), p.406-411

2021

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Postpartum Anti-N-methyl-D-aspartate Receptor Encephalitis: A Case Report and Literature Review

Internal Medicine, 2017/02/01, Vol.56(3), pp.357-362

2017

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SS18-SSX, the Oncogenic Fusion Protein in Synovial Sarcoma, Is a Cellular Context-Dependent Epigenetic Modifier

PloS one, 2015-11, Vol.10 (11), p.e0142991-e0142991

2015

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First pathological report of a de novo CD5‐positive diffuse large B‐cell lymphoma patient presenting with Guillain–Barré syndrome‐like neuropathy due to neurolymphomatosis

Neuropathology, 2018-08, Vol.38 (4), p.417-421

2018

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α -Synuclein coaggregation in familial amyotrophic lateral sclerosis with SOD1 gene mutation

Human pathology, 2013-06, Vol.44 (6), p.1171-1176

2013

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Tafamidis dramatically improved severe proteinuria in a patient with TTR V30M hereditary ATTR amyloidosis

Amyloid, 2019-04, Vol.26 (2), p.99-100

2019

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Sjögren syndrome-related plasma cell disorder and multifocal nodular AL amyloidosis: clinical picture and pathological findings

Amyloid, 2019-10, Vol.26 (4), p.225-233

2019

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Slowly progressing lower motor neuron disease caused by a novel duplication mutation in exon 1 of the SOD1 gene

Neurobiology of aging, 2014-10, Vol.35 (10), p.2420.e7-2420.e12

2014

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Extensive brain pathology in a patient with aceruloplasminemia with a prolonged duration of illness

Human pathology, 2012-03, Vol.43 (3), p.451-456

2012

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Clinical and Neuropathological Study of an Autopsied Case of Familial ALS with SOD1 Mutation with Very Long Survival (P5.051)

Neurology, 2016-04, Vol.86 (16_supplement)

2016

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Hypertrophic pachymeningitis is a characteristic manifestation of granulomatosis with polyangiitis: A retrospective study of anti‐neutrophil cytoplasmic antibody‐associated vasculitis

International journal of rheumatic diseases, 2017-04, Vol.20 (4), p.489-496

2017

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Elevation of serum heat-shock protein levels in amyotrophic lateral sclerosis

Neurological sciences, 2016-08, Vol.37 (8), p.1277-1281

2016

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Axonal TDP-43 aggregates in sporadic amyotrophic lateral sclerosis

Elevated serum levels of heat-shock protein (HSP) 70 and 90 in patients with ALS

Communication support project for patients with an intractable neurological disease

Suspected adverse effects after human papillomavirus vaccination: a temporal relationship

The broad symptoms with genetically identified episodic ataxia type 2 in a family

New criteria of suspected adverse symptoms related human papillomavirus vaccination

Patients with ALS under tracheostomy positive-pressure ventilation (TPPV) and complicating malignant tumor

Clinical features and treatment outcome of four patients with anti-signal recognition particle antibody positive necrotizing myopathy

Mixed connective tissue disease with interstitial pneumonia in HTLV-1 carrier: case report and review of the literature

Peripheral Sympathetic Nerve Dysfunction in Adolescent Japanese Girls Following Immunization with the Human Papillomavirus Vaccine

Suspected Adverse Effects After Human Papillomavirus Vaccination: A Temporal Relationship Between Vaccine Administration and the Appearance of Symptoms in Japan

Mutant IDH1 Dysregulates the Differentiation of Mesenchymal Stem Cells in Association with Gene-Specific Histone Modifications to Cartilage- and Bone-Related Genes

A Long-Term Observation on the Possible Adverse Effects in Japanese Adolescent Girls after Human Papillomavirus Vaccination

Spread of vimentin‐immunoreactive cells within the plaque‐like lesion in the spinal anterior horn of a patient with post‐poliomyelitis syndrome

Postpartum Anti-N-methyl-D-aspartate Receptor Encephalitis: A Case Report and Literature Review

SS18-SSX, the Oncogenic Fusion Protein in Synovial Sarcoma, Is a Cellular Context-Dependent Epigenetic Modifier

First pathological report of a de novo CD5‐positive diffuse large B‐cell lymphoma patient presenting with Guillain–Barré syndrome‐like neuropathy due to neurolymphomatosis

α -Synuclein coaggregation in familial amyotrophic lateral sclerosis with SOD1 gene mutation

Tafamidis dramatically improved severe proteinuria in a patient with TTR V30M hereditary ATTR amyloidosis

Sjögren syndrome-related plasma cell disorder and multifocal nodular AL amyloidosis: clinical picture and pathological findings

Slowly progressing lower motor neuron disease caused by a novel duplication mutation in exon 1 of the SOD1 gene

Extensive brain pathology in a patient with aceruloplasminemia with a prolonged duration of illness

Clinical and Neuropathological Study of an Autopsied Case of Familial ALS with SOD1 Mutation with Very Long Survival (P5.051)

Hypertrophic pachymeningitis is a characteristic manifestation of granulomatosis with polyangiitis: A retrospective study of anti‐neutrophil cytoplasmic antibody‐associated vasculitis

Elevation of serum heat-shock protein levels in amyotrophic lateral sclerosis

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