Hereditary ATTR Amyloidosis with Cardiomyopathy Caused by the Novel Variant Transthyretin Y114S (p.Y134S)-Reference-Cited by-同舟云学术

Hereditary ATTR Amyloidosis with Cardiomyopathy Caused by the Novel Variant Transthyretin Y114S (p.Y134S)

Published:2019-09-15 Issue:18 Volume:58 Page:2695-2698
ISSN:0918-2918
Container-title:Internal Medicine
language:en
Short-container-title:Intern. Med.

Author:

Nakase Taku¹,Yamashita Taro¹²,Matsuo Yoshimasa¹,Nomura Toshiya¹,Sasada Keiko³,Masuda Teruaki¹,Misumi Yohei¹,Takamatsu Kotaro¹,Oda Seitaro⁴,Furukawa Yutaro⁵,Obayashi Konen⁶,Matsui Hirotaka³⁷,Ando Yukio¹,Ueda Mitsuharu¹

Affiliation:

1. Department of Neurology, Graduate School of Medical Sciences, Kumamoto University, Japan

2. Amyloidosis Medical Practice Center, Kumamoto University Hospital, Japan

3. Department of Laboratory Medicine, Kumamoto University Hospital, Japan

4. Department of Diagnostic Radiology, Graduate School of Medical Sciences, Kumamoto University, Japan

5. Department of Cardiology, Oita Japanese Red Cross Hospital, Japan

6. Department of Morphological and Physiological Sciences, Graduate School of Medical Sciences, Kumamoto University, Japan

7. Department of Molecular Laboratory Medicine, Graduate School of Medical Sciences, Kumamoto University, Japan

Publisher

Japanese Society of Internal Medicine

Subject

General Medicine,Internal Medicine

Link

https://www.jstage.jst.go.jp/article/internalmedicine/58/18/58_2456-18/_pdf

Reference17 articles.

1. 1. Benson MD, Buxbaum JN, Eisenberg DS, et al. Amyloid nomenclature 2018: recommendations by the International Society of Amyloidosis (ISA) nomenclature committee. Amyloid 7: 1-5, 2019.

2. 2. Ando Y, Nakamura M, Araki S. Transthyretin-related familial amyloidotic polyneuropathy. Arch Neurol 62: 1057-1062, 2005.

3. 3. Sekijima Y, Ueda M, Koike H, Misawa S, Ishii T, Ando Y. Diagnosis and management of transthyretin familial amyloid polyneuropathy in Japan: red-flag symptom clusters and treatment algorithm. Orphanet J Rare Dis 13: 6, 2018.

4. 4. Masuda T, Ueda M, Kitajima M, et al. Teaching neuroImages: morphology of lumbosacral dorsal root ganglia and plexus in hereditary transthyretin amyloidosis. Neurology 91: e1834-e1835, 2018.

5. 5. Koike H, Misu K, Ikeda S, et al.; Study Group for Hereditary Neuropathy in Japan. Type I (transthyretin Met30) familial amyloid polyneuropathy in Japan: early- vs late-onset form. Arch Neurol 59: 1771-1776, 2002.

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