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Results 1 - 10 of 44 for Hypertrophic cardiomyopathy 9
  1. Familial hypertrophic cardiomyopathy 
    ... HYPERTROPHIC, 18; CMH18 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 20; CMH20 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9; CMH9 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 21; CMH21 CARDIOMYOPATHY, FAMILIAL ...
    https://medlineplus.gov/.../familial-hypertrophic-cardiomyopathy - Genetics
  2. Arrhythmogenic right ventricular cardiomyopathy 
    ... Lamin A/C gene mimic arrhythmogenic right ventricular cardiomyopathy. Eur Heart J. 2012 May;33(9):1128-36. doi: 10.1093/eurheartj/ehr451. Epub 2011 Dec 23. Citation on PubMed Taylor M, Graw S, Sinagra G, ... ventricular cardiomyopathy-overlap syndromes. Circulation. 2011 Aug 23;124(8): ...
    https://medlineplus.gov/...hmogenic-right-ventricular-cardiomyopathy - Genetics
  3. X-linked dilated cardiomyopathy 
    ... MA, Mateddu A, Muntoni F. X-linked dilated cardiomyopathy and the dystrophin gene. Neuromuscul Disord. 1999 Jul;9(5):339-46. doi: 10.1016/s0960-8966( ... Citation on PubMed Nakamura A. X-Linked Dilated Cardiomyopathy: A ... Pharmaceuticals (Basel). 2015 Jun 9;8(2):303-20. doi: 10.3390/ph8020303. ...
    https://medlineplus.gov/.../x-linked-dilated-cardiomyopathy - Genetics
  4. Familial dilated cardiomyopathy 
    ... 2011: clinical and genetic issues in familial dilated cardiomyopathy. J Am Coll Cardiol. 2011 Apr 19;57(16):1641-9. doi: 10.1016/j.jacc.2011.01.015. Citation on PubMed or Free article on PubMed Central Morales A, ... evaluation of dilated cardiomyopathy. Curr Cardiol Rep. 2013 Jul;15(7):375. ...
    https://medlineplus.gov/.../familial-dilated-cardiomyopathy - Genetics
  5. Keratoderma with woolly hair 
    ... 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. ...
    https://medlineplus.gov/.../condition/keratoderma-with-woolly-hair - Genetics
  6. Left ventricular noncompaction 
    ... Lorts A, Jefferies JL. Left ventricular non-compaction cardiomyopathy. Lancet. 2015 Aug 22;386(9995):813-25. doi: 10.1016/S0140-6736(14)61282-4. Epub 2015 Apr 9. Citation on PubMed Wang C, Takasaki A, Watanabe ...
    https://medlineplus.gov/.../condition/left-ventricular-noncompaction - Genetics
  7. Alpha-N-acetylgalactosaminidase deficiency 
    ... new infantile case of alpha-N-acetylgalactosaminidase deficiency. Cardiomyopathy ... Garman SC. The 1.9 a structure of human alpha-N-acetylgalactosaminidase: The ...
    https://medlineplus.gov/...lpha-n-acetylgalactosaminidase-deficiency - Genetics
  8. Mitochondrial trifunctional protein deficiency 
    ... 488-97. doi: 10.1007/s10545-009-1125-9. Epub 2009 Apr 29. Citation on PubMed Spiekerkoetter U, Mueller M, Cloppenburg E, Motz R, Mayatepek E, Bueltmann B, Korenke C. Intrauterine cardiomyopathy and cardiac mitochondrial proliferation in mitochondrial trifunctional protein ( ...
    https://medlineplus.gov/...hondrial-trifunctional-protein-deficiency - Genetics
  9. Glycogen storage disease type 0 
    ... Forsander G, Jotorp P, Oldfors A, Holme E. Cardiomyopathy and exercise intolerance ... J Pediatr Endocrinol Metab. 2012;25(9-10):963-7. doi: 10.1515/jpem-2012- ...
    https://medlineplus.gov/.../glycogen-storage-disease-type-0 - Genetics
  10. Barth syndrome 
    ... characterized by an enlarged and weakened heart (dilated cardiomyopathy), weakness in muscles used for movement (skeletal myopathy), ... in males.In males with Barth syndrome, dilated cardiomyopathy is often present at birth or develops within ...
    https://medlineplus.gov/genetics/condition/barth-syndrome - Genetics
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