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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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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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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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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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Echocardiographic Assessment of the Cardiac Amyloidoses

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

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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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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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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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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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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Cerebral amyloid angiopathy in posttransplant patients with hereditary ATTR amyloidosis

Neurology, 2016-08, Vol.87 (8), p.773-781

2016

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Carpal tunnel syndrome: a common initial symptom of systemic wild-type ATTR (ATTRwt) amyloidosis

Amyloid, 2016-01, Vol.23 (1), p.58-63

2016

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Repurposing diflunisal for familial amyloid polyneuropathy: a randomized clinical trial

JAMA : the journal of the American Medical Association, 2013-12, Vol.310 (24), p.2658

2013

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Genotype-phenotype correlation in Japanese patients with familial Mediterranean fever: differences in genotype and clinical features between Japanese and Mediterranean populations

Arthritis research & therapy, 2014-09, Vol.16 (5), p.439-439, Article 439

2014

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Liver Transplantation for Hereditary Transthyretin Amyloidosis: After 20 Years Still the Best Therapeutic Alternative?

Transplantation, 2015-09, Vol.99 (9), p.1847-1854

2015

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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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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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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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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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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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Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP): Estimation of pathological lesion stage from brain images

Journal of the neurological sciences, 2024-06, Vol.461, p.123027-123027, Article 123027

2024

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

Schwann cell and endothelial cell damage in transthyretin familial amyloid polyneuropathy

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

Guideline of transthyretin-related hereditary amyloidosis for clinicians

Echocardiographic Assessment of the Cardiac Amyloidoses

Amyloid neuropathy and autonomic dysfunction

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

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

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

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

Cerebral amyloid angiopathy in posttransplant patients with hereditary ATTR amyloidosis

Carpal tunnel syndrome: a common initial symptom of systemic wild-type ATTR (ATTRwt) amyloidosis

Repurposing diflunisal for familial amyloid polyneuropathy: a randomized clinical trial

Genotype-phenotype correlation in Japanese patients with familial Mediterranean fever: differences in genotype and clinical features between Japanese and Mediterranean populations

Liver Transplantation for Hereditary Transthyretin Amyloidosis: After 20 Years Still the Best Therapeutic Alternative?

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

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

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

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

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

Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP): Estimation of pathological lesion stage from brain images

Pathogenesis of and therapeutic strategies to ameliorate the transthyretin amyloidoses

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

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

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

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