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JCS 2020 Guideline on Diagnosis and Treatment of Cardiac Amyloidosis

Circulation Journal, 2020/08/25, Vol.84(9), pp.1610-1671

2020

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Citrin Deficiency: Clinical and Nutritional Features

Nutrients, 2023-05, Vol.15 (10), p.2284

2023

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Distribution of amyloidosis subtypes based on tissue biopsy site − Consecutive analysis of 729 patients at a single amyloidosis center in Japan

Pathology international, 2021-01, Vol.71 (1), p.70-79

2021

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Nationwide Survey of 741 Patients with Systemic Amyloid Light-chain Amyloidosis in Japan

Internal Medicine, 2018/01/15, Vol.57(2), pp.181-187

2018

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Renal Function in Aged C57BL/6J Mice Is Impaired by Deposition of Age-Related Apolipoprotein A-II Amyloid Independent of Kidney Aging

The American journal of pathology, 2023-06, Vol.193 (6), p.725-739

2023

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Ocular findings in patients with acquired ATTRv amyloidosis following domino liver transplantation

PloS one, 2023-09, Vol.18 (9), p.e0291716-e0291716

2023

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Transthyretin Variant Amyloidosis with a TTR A97D (p.A117D) Mutation Manifesting Remarkable Asymmetric Neuropathy

Internal Medicine, 2023/08/01, Vol.62(15), pp.2261-2266

2023

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Amyloid-Forming Corpora Amylacea and Spheroid-Type Amyloid Deposition: Comprehensive Analysis Using Immunohistochemistry, Proteomics, and a Literature Review

International journal of molecular sciences, 2024-04, Vol.25 (7), p.4040

2024

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First nationwide survey on systemic wild-type ATTR amyloidosis in Japan

Amyloid, 2018-01, Vol.25 (1), p.8-10

2018

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Analysis of daily energy, protein, fat, and carbohydrate intake in citrin-deficient patients: Towards prevention of adult-onset type II citrullinemia

Molecular genetics and metabolism, 2021-05, Vol.133 (1), p.63-70

2021

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Reversible Leukoencephalopathy in a Man with Childhood-onset Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome

Internal Medicine, 2022/02/15, Vol.61(4), pp.553-557

2022

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An autopsy case of amyloid tubulopathy exhibiting characteristic spheroid-type deposition

Virchows Archiv : an international journal of pathology, 2020-07, Vol.477 (1), p.157-163

2020

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Giant Hepatomegaly with Spleno-testicular Enlargement in a Patient with Apolipoprotein A-I Amyloidosis: An Uncommon Type of Amyloidosis in Japan

Internal Medicine, 2021/02/15, Vol.60(4), pp.575-581

2021

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Development of diagnostic antibodies against immunoglobulin heavy chain variable region for heavy chain amyloidosis (AH amyloidosis)

Pathology international, 2021-04, Vol.71 (4), p.245-254

2021

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Distribution and progression of cerebral amyloid angiopathy in early-onset V30M (p.V50M) hereditary ATTR amyloidosis

Amyloid, 2023-01, Vol.30 (1), p.109-118

2023

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Anterior horn damage in brachial multisegmental amyotrophy with superficial siderosis and dural tear: an autopsy case report

BMC neurology, 2023-03, Vol.23 (1), p.129-129, Article 129

2023

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Macrophages in the reticuloendothelial system inhibit early induction stages of mouse apolipoprotein A-II amyloidosis

Amyloid, 2023-04, Vol.30 (2), p.225-238

2023

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AH amyloid neuropathy: a novel clinical phenotype confirmed by histopathology and mass spectrometry

Amyloid, 2022-04, Vol.29 (2), p.141-142

2022

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Hereditary Fibrinogen Aα-Chain Amyloidosis in Asia: Clinical and Molecular Characteristics

International journal of molecular sciences, 2018-01, Vol.19 (1), p.320

2018

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Late-onset Hereditary ATTR Amyloidosis with a Novel p.P63S (P43S) Transthyretin Variant

Internal Medicine, 2021/02/15, Vol.60(4), pp.557-561

2021

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Late-onset familial Mediterranean fever in Japan

Modern rheumatology, 2020-05, Vol.30 (3), p.564-567

2020

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Food Preferences of Patients with Citrin Deficiency

Nutrients, 2021-09, Vol.13 (9), p.3123

2021

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Usefulness of gastroduodenal biopsy in the differential diagnosis of systemic AH amyloidosis from systemic AL amyloidosis

Histopathology, 2018-08, Vol.73 (2), p.230-239

2018

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A case of spheroid‐type localized lactoferrin amyloidosis in the bronchus

Pathology international, 2019-04, Vol.69 (4), p.235-240

2019

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Renal AH Amyloidosis Associated With a Truncated Immunoglobulin Heavy Chain Undetectable by Immunostaining

American journal of kidney diseases, 2015-12, Vol.66 (6), p.1095-1100

2015

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JCS 2020 Guideline on Diagnosis and Treatment of Cardiac Amyloidosis

Citrin Deficiency: Clinical and Nutritional Features

Distribution of amyloidosis subtypes based on tissue biopsy site − Consecutive analysis of 729 patients at a single amyloidosis center in Japan

Nationwide Survey of 741 Patients with Systemic Amyloid Light-chain Amyloidosis in Japan

Renal Function in Aged C57BL/6J Mice Is Impaired by Deposition of Age-Related Apolipoprotein A-II Amyloid Independent of Kidney Aging

Ocular findings in patients with acquired ATTRv amyloidosis following domino liver transplantation

Transthyretin Variant Amyloidosis with a TTR A97D (p.A117D) Mutation Manifesting Remarkable Asymmetric Neuropathy

Amyloid-Forming Corpora Amylacea and Spheroid-Type Amyloid Deposition: Comprehensive Analysis Using Immunohistochemistry, Proteomics, and a Literature Review

First nationwide survey on systemic wild-type ATTR amyloidosis in Japan

Analysis of daily energy, protein, fat, and carbohydrate intake in citrin-deficient patients: Towards prevention of adult-onset type II citrullinemia

Reversible Leukoencephalopathy in a Man with Childhood-onset Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome

An autopsy case of amyloid tubulopathy exhibiting characteristic spheroid-type deposition

Giant Hepatomegaly with Spleno-testicular Enlargement in a Patient with Apolipoprotein A-I Amyloidosis: An Uncommon Type of Amyloidosis in Japan

Development of diagnostic antibodies against immunoglobulin heavy chain variable region for heavy chain amyloidosis (AH amyloidosis)

Distribution and progression of cerebral amyloid angiopathy in early-onset V30M (p.V50M) hereditary ATTR amyloidosis

Anterior horn damage in brachial multisegmental amyotrophy with superficial siderosis and dural tear: an autopsy case report

Macrophages in the reticuloendothelial system inhibit early induction stages of mouse apolipoprotein A-II amyloidosis

AH amyloid neuropathy: a novel clinical phenotype confirmed by histopathology and mass spectrometry

Hereditary Fibrinogen Aα-Chain Amyloidosis in Asia: Clinical and Molecular Characteristics

Late-onset Hereditary ATTR Amyloidosis with a Novel p.P63S (P43S) Transthyretin Variant

Late-onset familial Mediterranean fever in Japan

Food Preferences of Patients with Citrin Deficiency

Usefulness of gastroduodenal biopsy in the differential diagnosis of systemic AH amyloidosis from systemic AL amyloidosis

A case of spheroid‐type localized lactoferrin amyloidosis in the bronchus

Renal AH Amyloidosis Associated With a Truncated Immunoglobulin Heavy Chain Undetectable by Immunostaining

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