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Amyloid fibril proteins and amyloidosis: chemical identification and clinical classification International Society of Amyloidosis 2016 Nomenclature Guidelines

Amyloid, 2016-10, Vol.23 (4), p.209-213

2016

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Nomenclature 2014: Amyloid fibril proteins and clinical classification of the amyloidosis

Amyloid, 2014-12, Vol.21 (4), p.221-224

2014

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Schwann cell and endothelial cell damage in transthyretin familial amyloid polyneuropathy

Neurology, 2016-11, Vol.87 (21), p.2220-2229

2016

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Guideline of transthyretin-related hereditary amyloidosis for clinicians

Orphanet journal of rare diseases, 2013-02, Vol.8 (1), p.31-31

2013

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Safety and efficacy of long-term diflunisal administration in hereditary transthyretin (ATTR) amyloidosis

Amyloid, 2015-06, Vol.22 (2), p.79-83

2015

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Amyloid neuropathy and autonomic dysfunction

Neurology and clinical neuroscience, 2022-05, Vol.10 (3), p.137-146

Ikeda, Shu‐ichi

2022

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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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Echocardiographic Assessment of the Cardiac Amyloidoses

Circulation Journal, 2015/03/25, Vol.79(4), pp.721-734

2015

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Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease

The New England journal of medicine, 2009-04, Vol.360 (17), p.1729-1739

2009

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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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Adult onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) and Nasu–Hakola disease: lesion staging and dynamic changes of axons and microglial subsets

Brain pathology (Zurich, Switzerland), 2017-11, Vol.27 (6), p.748-769

2017

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Pathogenesis of and therapeutic strategies to ameliorate the transthyretin amyloidoses

Current pharmaceutical design, 2008-10, Vol.14 (30), p.3219-3230

2008

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A 67‐Year‐Old Man with Leg Weakness and Hypertrophic Cardiomyopathy

Brain pathology (Zurich, Switzerland), 2020-03, Vol.30 (2), p.427-428

2020

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High prevalence of wild-type transthyretin deposition in patients with idiopathic carpal tunnel syndrome: a common cause of carpal tunnel syndrome in the elderly

Human pathology, 2011-11, Vol.42 (11), p.1785-1791

2011

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Markers for Guillain‐Barré syndrome with poor prognosis: a multi‐center study

Journal of the peripheral nervous system, 2017-12, Vol.22 (4), p.433-439

2017

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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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Diflunisal stabilizes familial amyloid polyneuropathy-associated transthyretin variant tetramers in serum against dissociation required for amyloidogenesis

Neuroscience research, 2006-12, Vol.56 (4), p.441-449

2006

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Clinical Manifestations at Diagnosis in Japanese Patients with Systemic AL Amyloidosis: A Retrospective Study of 202 Cases with a Special Attention to Uncommon Symptoms

Internal Medicine, 2014, Vol.53(5), pp.403-412

2014

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Principal component analysis for ataxic gait using a triaxial accelerometer

Journal of neuroengineering and rehabilitation, 2017-05, Vol.14 (1), p.37-37, Article 37

2017

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Prevalence of Fabry disease and GLA c.196G>C variant in Japanese stroke patients

Journal of human genetics, 2017-07, Vol.62 (7), p.665-670

2017

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Matrix metalloproteinase-2 ablation in dystrophin-deficient mdx muscles reduces angiogenesis resulting in impaired growth of regenerated muscle fibers

Human molecular genetics, 2011-05, Vol.20 (9), p.1787-1799

2011

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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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Brain Biopsy Is More Reliable than the DNA test for JC Virus in Cerebrospinal Fluid for the Diagnosis of Progressive Multifocal Leukoencephalopathy

Internal Medicine, 2017/05/15, Vol.56(10), pp.1231-1234

2017

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Distinctive features of degenerating Purkinje cells in spinocerebellar ataxia type 31

Neuropathology, 2014-06, Vol.34 (3), p.261-267

2014

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Advantage of administering tacrolimus for improving prognosis of patients with polymyositis and dermatomyositis

International journal of rheumatic diseases, 2016-12, Vol.19 (12), p.1322-1330

2016

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Amyloid fibril proteins and amyloidosis: chemical identification and clinical classification International Society of Amyloidosis 2016 Nomenclature Guidelines

Nomenclature 2014: Amyloid fibril proteins and clinical classification of the amyloidosis

Schwann cell and endothelial cell damage in transthyretin familial amyloid polyneuropathy

Guideline of transthyretin-related hereditary amyloidosis for clinicians

Safety and efficacy of long-term diflunisal administration in hereditary transthyretin (ATTR) amyloidosis

Amyloid neuropathy and autonomic dysfunction

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

Echocardiographic Assessment of the Cardiac Amyloidoses

Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease

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

Adult onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) and Nasu–Hakola disease: lesion staging and dynamic changes of axons and microglial subsets

Pathogenesis of and therapeutic strategies to ameliorate the transthyretin amyloidoses

A 67‐Year‐Old Man with Leg Weakness and Hypertrophic Cardiomyopathy

High prevalence of wild-type transthyretin deposition in patients with idiopathic carpal tunnel syndrome: a common cause of carpal tunnel syndrome in the elderly

Markers for Guillain‐Barré syndrome with poor prognosis: a multi‐center study

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

Diflunisal stabilizes familial amyloid polyneuropathy-associated transthyretin variant tetramers in serum against dissociation required for amyloidogenesis

Clinical Manifestations at Diagnosis in Japanese Patients with Systemic AL Amyloidosis: A Retrospective Study of 202 Cases with a Special Attention to Uncommon Symptoms

Principal component analysis for ataxic gait using a triaxial accelerometer

Prevalence of Fabry disease and GLA c.196G>C variant in Japanese stroke patients

Matrix metalloproteinase-2 ablation in dystrophin-deficient mdx muscles reduces angiogenesis resulting in impaired growth of regenerated muscle fibers

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

Brain Biopsy Is More Reliable than the DNA test for JC Virus in Cerebrospinal Fluid for the Diagnosis of Progressive Multifocal Leukoencephalopathy

Distinctive features of degenerating Purkinje cells in spinocerebellar ataxia type 31

Advantage of administering tacrolimus for improving prognosis of patients with polymyositis and dermatomyositis

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