V122I Transthyretin Cardiomyopathy
Author:
Publisher
Elsevier BV
Subject
Cardiology and Cardiovascular Medicine
Reference9 articles.
1. Recent advances in the diagnosis and management of cardiac amyloidosis;Sher;Future Cardiol,2014
2. Association of the V122I hereditary transthyretin amyloidosis genetic variant with heart failure among individuals of African or Hispanic/Latino ancestry;Damrauer;JAMA,2019
3. Significance of the amyloidogenic transthyretin Val 122 Ile allele in African Americans in the Arteriosclerosis Risk in Communities (ARIC) and Cardiovascular Health (CHS) studies;Buxbaum;Am Heart J,2010
4. The amyloidogenic V122I transthyretin variant in elderly black Americans;Quarta;N Engl J Med,2015
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Cited by 4 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. Cardiovascular Burden of the V142I Transthyretin Variant;JAMA;2024-06-04
2. Deep phenotyping of p.(V142I)‐associated variant transthyretin amyloid cardiomyopathy: Distinct from wild‐type transthyretin amyloidosis?;European Journal of Heart Failure;2024-01-28
3. Extending the reach of expert amyloidosis care: A feasibility study exploring the staged implementation of a UK amyloidosis network;Clinical Medicine;2024-01
4. Prevalence and Outcomes of p.Val142Ile TTR Amyloidosis Cardiomyopathy: A Systematic Review;Circulation: Genomic and Precision Medicine;2021-10
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