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Results 1 - 10 of 19 for Hypertrophic cardiomyopathy 21
  1. ... Kaya CT, Sayin T, Heper AO, Tekin M. Cardiomyopathy with alopecia and palmoplantar keratoderma (CAPK) is caused by a JUP mutation. Br J Dermatol. 2011 Oct;165(4):917-21. doi: 10.1111/j.1365-2133.2011.10455. ...
  2. ... Terzic A. ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gating. Nat Genet. 2004 Apr;36(4):382-7. doi: 10.1038/ng1329. Epub 2004 Mar 21. Citation on PubMed or Free article on PubMed ...
  3. ... MA, Mateddu A, Muntoni F. X-linked dilated cardiomyopathy and the dystrophin ... 2010 May 21. Citation on PubMed Muntoni F, Torelli S, Ferlini ...
  4. ... cause a novel early-onset myopathy with fatal cardiomyopathy. Ann Neurol. 2007 ... Epub 2014 Jul 21. Citation on PubMed Fukuzawa A, Lange S, Holt ...
  5. ... Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon ... 2023 Jul 21. Citation on PubMed
  6. ... status in skeletal muscle. Physiology (Bethesda). 2006 Feb;21:48-60. doi: ... with conduction system disease and muscular glycogenosis. Neuromuscul ...
  7. ... males and is characterized by a weakened heart (cardiomyopathy), muscle weakness, recurrent infections, and short stature. TAFAZZIN ... Condition MedlinePlus Genetics provides information about Familial dilated cardiomyopathy More About This Health Condition MedlinePlus Genetics provides ...
  8. ... muscle is also weakened, which is known as cardiomyopathy. This abnormality prevents the heart from pumping normally. ... H, Honzik T, Zeman J, Linhart A. Hypertrophic cardiomyopathy due to the mitochondrial DNA mutation m.3303C> ...
  9. ... Condition CAV3 gene mutations also can cause hypertrophic cardiomyopathy. Hypertrophic cardiomyopathy is a thickening of the heart (cardiac) muscle ... failure.When caused by CAV3 gene mutations, hypertrophic cardiomyopathy as well as limb-girdle muscular dystrophy, isolated ...
  10. ... more likely to have a weakened heart muscle (cardiomyopathy) than people with myofibrillar myopathy caused by mutations in other genes. In some cases, cardiomyopathy is the first symptom of this condition. More ...
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