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Familial restrictive cardiomyopathy is an autosomal dominant cardiomyopathy histologically characterized by myocyte hypertrophy and interstitial fibrosis. The case of a 54-year-old man diagnosed with restrictive cardiomyopathy is reported. The patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::026c83cf499dfc98ae808f6e6d9035c6
https://europepmc.org/articles/PMC2359625/
https://europepmc.org/articles/PMC2359625/
Autor:
Cubero GI; Servicio de Cardiología, Hospital Central de Asturias, Julián Clavería s/n, Oviedo, Spain., Larraya GL, Reguero JR
Publikováno v:
Experimental and clinical cardiology [Exp Clin Cardiol] 2007 Spring; Vol. 12 (1), pp. 54-5.