Adult patients with Fabry disease: what does the cardiologist need to know?: Table 1
Author:
Publisher
BMJ
Subject
Cardiology and Cardiovascular Medicine
Reference8 articles.
1. Fabry disease;Germain;Orphanet J Rare Dis,2010
2. Tissue-specific X chromosome inactivation studies as a decision-making criteria for enzyme replacement therapy in female heterozygotes for Fabry disease;Germain;Mol Genet Metab,2014
3. Cardiac manifestations of Anderson-Fabry disease: results from the international Fabry outcome survey;Linhart;Eur Heart J,2007
4. Natural course of Fabry disease: changing pattern of causes of death in FOS—Fabry Outcome Survey;Mehta;J Med Genet,2009
5. Clinical and genetic predictors of major cardiac events in patients with Anderson–Fabry disease;Patel;Heart
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1. New mutation in Fabry disease: c.448delG, first phenotypic description;Molecular Genetics and Metabolism Reports;2021-06
2. Hypertrophic Cardiomyopathy and Primary Restrictive Cardiomyopathy: Similarities, Differences and Phenocopies;Journal of Clinical Medicine;2021-05-01
3. Fabry disease in cardiology practice: Literature review and expert point of view;Archives of Cardiovascular Diseases;2019-04
4. Recommendations for the inclusion of Fabry disease as a rare febrile condition in existing algorithms for fever of unknown origin;Internal and Emergency Medicine;2017-07-19
5. Maladie de Fabry: à propos d’un cas atypique;Pan African Medical Journal;2017
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