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Nov 26, 2014 (publication date) through Dec 26, 2024
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World Journal of Cardiology
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1949-8462
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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Tariq M, Ware SM. Importance of genetic evaluation and testing in pediatric cardiomyopathy. World J Cardiol 2014; 6(11): 1156-1165 [PMID: 25429328 DOI: 10.4330/wjc.v6.i11.1156] |
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| URL: | https://www.wjgnet.com/1949-8462/full/v6/i11/1156.htm |
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I. V. Leontyeva, V. V. Presova. Hypertrophic cardiomyopathy in an athlete, occurring under the mask of sports remodeling. Secondary prevention of sudden cardiac death. Analysis of a clinical case. Russian Journal for Personalized Medicine 2023; 3(2): 98 doi: 10.18705/2782-38062023-3-2-98-106
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Michael B. Rosamilia, Alexandra M. Markunas, Priya S. Kishnani, Andrew P. Landstrom. Underrepresentation of Diverse Ancestries Drives Uncertainty in Genetic Variants Found in Cardiomyopathy-Associated Genes. JACC: Advances 2024; 3(2): 100767 doi: 10.1016/j.jacadv.2023.100767
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Deema Aljeaid, Ana Isabel Sanchez, Emily Wakefield, Sarah E. Chadwell, Nicole Moore, Carlos E. Prada, Wenying Zhang. Prevalence of pathogenic and likely pathogenic variants in the RASopathy genes in patients who have had panel testing for cardiomyopathy. American Journal of Medical Genetics Part A 2019; 179(4): 608 doi: 10.1002/ajmg.a.61072
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Teresa M. Lee, Stephanie M. Ware. Toward personalized medicine: Does genetic diagnosis of pediatric cardiomyopathy influence patient management?. Progress in Pediatric Cardiology 2015; 39(1): 43 doi: 10.1016/j.ppedcard.2015.01.008
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Jeffrey Schubert, Muhammad Tariq, Gabrielle Geddes, Steven Kindel, Erin M. Miller, Stephanie M. Ware. Novel pathogenic variants in filamin C identified in pediatric restrictive cardiomyopathy. Human Mutation 2018; 39(12): 2083 doi: 10.1002/humu.23661
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