Symptomatic Val122del mutated hereditary transthyretin amyloidosis: Need for early diagnosis and prioritization for heart and liver transplantation-Reference-Cited by-同舟云学术

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Symptomatic Val122del mutated hereditary transthyretin amyloidosis: Need for early diagnosis and prioritization for heart and liver transplantation

Published:2021-08 Issue:4 Volume:20 Page:323-329
ISSN:1499-3872
Container-title:Hepatobiliary & Pancreatic Diseases International
language:en
Short-container-title:Hepatobiliary & Pancreatic Diseases International

Author:

Schettini Adriano-Valerio,Llado Laura,Heimbach Julie K,Costello Jose Gonzalez,Tranäng Marie,Van Caenegem Olivier,Daly Richard C,Van den Bergh Peter,Casasnovas Carlos,Fabregat Joan,Poterucha John J,Foguenne Maxime,Ericzon Bo Göran,Lerut Jan

Publisher

Elsevier BV

Subject

Gastroenterology,Hepatology

Reference52 articles.

1. Forty years of experience with type I amyloid neuropathy: review of 483 cases;Coutinho,1980

2. Wilczek HE; FAPWTRʼs investigators. Survival after transplantation in patients with mutations other than Val30Met: Extracts from the FAP World Transplant Registry;Suhr;Transplantation,2016

3. Liver transplantation in transthyretin amyloidosis: issues and challenges;Carvalho;Liver Transpl,2015

4. Tafamidis treatment for patients with transthyretin amyloid cardiomyopathy;Maurer;N Engl J Med,2018

5. Inotersen treatment for patients with hereditary transthyretin amyloidosis;Benson;N Engl J Med,2018

Cited by 1 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. Advancing immunosuppression in liver transplantation: A narrative review;Hepatobiliary & Pancreatic Diseases International;2024-10

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