Low Prevalence of Clinically Apparent Cardiac Amyloidosis Among Carriers of Transthyretin V122I Variant in a Large Electronic Medical Record
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference6 articles.
1. Amyloid diseases of the heart: assessment, diagnosis, and referral;Dubrey;Heart,2011
2. Transthyretin familial amyloid polyneuropathy;Planté-Bordeneuve;Handb Clin Neurol,2013
3. Variant-sequence transthyretin (isoleucine 122) in late-onset cardiac amyloidosis in black Americans;Jacobson;N Eng J Med,1997
4. 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
5. Prospective evaluation of the morbidity and mortality of wild-type and V122I mutant transthyretin amyloid cardiomyopathy: the Transthyretin Amyloidosis Cardiac Study (TRACS).;Ruberg;Am Heart J,2012
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2. Practical Guidance for the Use of Patisiran in the Management of Polyneuropathy in Hereditary Transthyretin-Mediated Amyloidosis;Therapeutics and Clinical Risk Management;2023-11
3. Gene Editing as the Future of Cardiac Amyloidosis Therapeutics;Current Problems in Cardiology;2023-08
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