Late-onset Transthyretin (TTR)-familial Amyloid Polyneuropathy (FAP) with a Long Disease Duration from Non-endemic Areas in Japan-Reference-Cited by-同舟云学术

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Late-onset Transthyretin (TTR)-familial Amyloid Polyneuropathy (FAP) with a Long Disease Duration from Non-endemic Areas in Japan

Published:2019-03-01 Issue:5 Volume:58 Page:713-718
ISSN:0918-2918
Container-title:Internal Medicine
language:en
Short-container-title:Intern. Med.

Author:

Miyake Zenshi¹,Nakamagoe Kiyotaka²,Ezawa Naoki³,Yoshinaga Tsuneaki³,Hashimoto Ryosuke⁴,Sato Taiki⁵,Sekijima Yoshiki³,Tamaoka Akira²

Affiliation:

1. Department of Neurology, University of Tsukuba Hospital, Japan

2. Department of Neurology, Faculty of Medicine, University of Tsukuba, Japan

3. Department of Medicine (Neurology and Rheumatology), Shinshu University School of Medicine, Japan

4. Department of Pathology, University of Tsukuba Hospital, Japan

5. Department of Diagnostic Pathology, Faculty of Medicine, University of Tsukuba, Japan

Publisher

Japanese Society of Internal Medicine

Subject

General Medicine,Internal Medicine

Link

https://www.jstage.jst.go.jp/article/internalmedicine/58/5/58_1457-18/_pdf

Reference15 articles.

1. 1. Ando Y. Amyloidosis and neurological disorders: treatable amyloidosis. Rinsho Shinkeigaku 55: 797-803, 2015 (in Japanese, Abstract in English).

2. 2. Westermark P, Benson MD, Buxbaum JN, et al. A primer of amyloid nomenclature. Amyloid 14: 179-183, 2007.

3. 3. Ando Y, Coelho T, Berk JL, et al. Guideline of transthyretin-related hereditary amyloidosis for clinicians. Orphanet J Rare Dis 8: 31-48, 2013.

4. 4. Koike H, Sobue G. Late-onset familial amyloid polyneuropathy in Japan. Amyloid 19: 55-57, 2012.

5. 5. Koike H, Nakamura T, Hashizume A, et al. Cardiac and peripheral vasomotor autonomic functions in late-onset transthyretin Val30Met familial amyloid polyneuropathy. J Neurol 264: 2293-2302, 2017.

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Phenotypic heterogeneity and diagnostic features of transthyretin amyloidosis with polyneuropathy;Neuromuscular Diseases;2021-12-13

2. Neuropathy Associated with Hereditary Transthyretin Amyloidosis—Diagnosis and Management;US Neurology;2020

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