Genetic counselling for at-risk family members with hereditary transthyretin amyloidosis: data from a single-centre study-Reference-Cited by-同舟云学术

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Genetic counselling for at-risk family members with hereditary transthyretin amyloidosis: data from a single-centre study

Published:2024-05-25 Issue:3 Volume:31 Page:179-183
ISSN:1350-6129
Container-title:Amyloid
language:en
Short-container-title:Amyloid

Author:

Nakamura Katsuya¹²,Yoshinaga Tsuneaki¹,Sakyu Akiko²,Matsushima Akira¹,Yonehara Yuka²,Kojima Tomomi²,Ishikawa Masumi²,Kise Emiko²,Kosho Tomoki²³,Sekijima Yoshiki¹

Affiliation:

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

2. Center for Medical Genetics, Shinshu University Hospital, Matsumoto, Japan

3. Department of Medical Genetics, Shinshu University School of Medicine, Matsumoto, Japan

Publisher

Informa UK Limited

Link

https://www.tandfonline.com/doi/pdf/10.1080/13506129.2024.2357094

Reference23 articles.

1. Diagnosis and management of transthyretin familial amyloid polyneuropathy in Japan: red-flag symptom clusters and treatment algorithm

2. Guideline of transthyretin-related hereditary amyloidosis for clinicians

3. Biochemical effect of liver transplantation in two Swedish patients with familial amyloidotic polyneuropathy (FAP-met30)

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

5. Tafamidis for transthyretin familial amyloid polyneuropathy: A randomized, controlled trial

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