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Results 1 - 10 of 72 for Hypertrophic cardiomyopathy 18
  1. ... HYPERTROPHIC, 15; CMH15 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 17; CMH17 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 18; CMH18 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 20; CMH20 CARDIOMYOPATHY, FAMILIAL ...
  2. ... MacLeod H, Dellefave-Castillo L. Arrhythmogenic Right Ventricular Cardiomyopathy Overview. 2005 Apr 18 [updated 2023 May 11]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews(R) [Internet]. ... cardiomyopathy: molecular genetics into clinical practice in the era ...
  3. ... mutation p.K217del in troponin T2, causing dilated cardiomyopathy. Neth Heart J. 2010 Oct;18(10):478-85. doi: 10.1007/BF03091819. Citation on PubMed or Free article on PubMed Central Rodriguez JE, McCudden ... cardiomyopathy: basic concepts and future molecular diagnostics. Clin Biochem. ...
  4. ... Novel mutations in sarcomeric protein genes in dilated cardiomyopathy. Biochem Biophys Res Commun. 2002 Oct 18;298(1):116-20. doi: 10.1016/s0006-291x(02)02374-4. Citation on PubMed Dong X, Fan P, Tian T, Yang ... ventricular noncompaction cardiomyopathy. Clin Chim Acta. 2017 Feb;465:40-44. ...
  5. ... not a causative mutation in arrhythmogenic right ventricular cardiomyopathy. Eur J Hum Genet. 2010 Jul;18(7):776-82. doi: 10.1038/ejhg.2010.19. Epub 2010 Mar 3. Citation on PubMed or Free article on PubMed Central ... cardiomyopathy caused by desmocollin-2 mutations. Cardiovasc Res. 2011 ...
  6. ... disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma. Hum Mol Genet. 2000 Nov 1;9(18):2761-6. doi: 10.1093/hmg/9.18. ...
  7. ... disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma. Hum Mol Genet. 2000 Nov 1;9(18):2761-6. doi: 10.1093/hmg/9.18. ...
  8. Cardiomyopathy in Children and Teens (American Academy of Pediatrics)  
    Cardiomyopathy is one of the common causes of sudden cardiac death in children under the age of 18. Here's what families need to know.
  9. About Duchenne Muscular Dystrophy From the National Institutes of Health (National Human Genome Research Institute)  
    Muscular Dystrophy/Genetics ... Muscular Dystrophy ... National Human Genome Research Institute ... From the National Institutes of Health ... Duchenne muscular dystrophy ...
  10. ... adulthood, often because of complications related to dilated cardiomyopathy, and some do not survive past infancy. DOLK-CDG is likely a rare condition; at least 18 cases have been reported in the scientific literature. ...
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