Screening for Fabry Disease in patients with unexplained left ventricular hypertrophy
Author:
Funder
Sanofi Genzyme
Hong Kong Special Administrative Region Government Health and Medical Research Fund
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference49 articles.
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2. The Molecular Defect Leading to Fabry Disease: Structure of Human α-Galactosidase;SC Garman;Journal of Molecular Biology,2004
3. Anderson-Fabry Disease: A Multiorgan Disease.;T Antonino;Current Pharmaceutical Design,2013
4. Clinical Features, Diagnosis, and Management of Patients With Anderson-Fabry Cardiomyopathy;H Yogasundaram;Can J Cardiol,2017
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1. Screening for Fabry disease in patients with left ventricular hypertrophy in China: A multicentre and prospective study;ESC Heart Failure;2024-09-03
2. The Asian Fabry Cardiomyopathy High-Risk Screening Study 2 (ASIAN-FAME-2): Prevalence of Fabry Disease in Patients with Left Ventricular Hypertrophy;Journal of Clinical Medicine;2024-07-02
3. Anderson–Fabry disease management: role of the cardiologist;European Heart Journal;2024-03-15
4. FDrisk: development of a validated risk assessment tool for Fabry disease utilizing electronic health record data;Journal of Rare Diseases;2024-01-04
5. Impact of GLA Variant Classification on the Estimated Prevalence of Fabry Disease: A Systematic Review and Meta-Analysis of Screening Studies;Circulation: Genomic and Precision Medicine;2023-12-04
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