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Dilated cardiomyopathy: causes, mechanisms, and current and future treatment approaches.
Heymans S, Lakdawala NK, Tschöpe C, Klingel K. Heymans S, et al. Lancet. 2023 Sep 16;402(10406):998-1011. doi: 10.1016/S0140-6736(23)01241-2. Lancet. 2023. PMID: 37716772 Review.
Dilated cardiomyopathy is conventionally defined as the presence of left ventricular or biventricular dilatation or systolic dysfunction in the absence of abnormal loading conditions (eg, primary valve disease) or significant coronary artery disease sufficien
Dilated cardiomyopathy is conventionally defined as the presence of left ventricular or biventricular dilatation or systolic d
Retrospective Analysis of Clinical Genetic Testing in Pediatric Primary Dilated Cardiomyopathy: Testing Outcomes and the Effects of Variant Reclassification.
Quiat D, Witkowski L, Zouk H, Daly KP, Roberts AE. Quiat D, et al. J Am Heart Assoc. 2020 Jun 2;9(11):e016195. doi: 10.1161/JAHA.120.016195. Epub 2020 May 27. J Am Heart Assoc. 2020. PMID: 32458740 Free PMC article.
Background Genetic testing in pediatric primary dilated cardiomyopathy (DCM) patients has identified numerous disease-causing variants, but few studies have evaluated genetic testing outcomes in this population in the context of patient and familial clinical …
Background Genetic testing in pediatric primary dilated cardiomyopathy (DCM) patients has identified numerous disease-c …