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pro vyhledávání: '"Amorim, Ingrid G"'
Autor:
de Morais, Rafael OB, Chaves-Markman, Ândrea V, Miranda, Anna PP, Amorim, Ingrid G, Cavalcanti, Maria da GA de M, Markman, Manuel, Markman-Filho, Brivaldo
Background: Pompe disease is a lysosomal storage disease with an autosomal recessive inheritance characterized by an insufficient activity of the acid alpha-glucosidase enzyme. The incidence varies from 1:40000 to 1:200000 live births and cardiac inv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b845aafa056732f233646e0355773207
https://europepmc.org/articles/PMC5944812/
https://europepmc.org/articles/PMC5944812/
Autor:
de Morais RO; Hospital Agamenon Magalhães, Department of Cardiology Brazil., Chaves-Markman ÂV; Hospital Agamenon Magalhães, Department of Cardiology Brazil.; Hospital das Clínicas da UFPE, Department of Cardiology Brazil., Miranda AP; Hospital das Clínicas da UFPE, Department of Neurology Brazil., Amorim IG; Hospital Maternidade Divino Amor Brazil., Cavalcanti MDGM; Hospital Agamenon Magalhães, Department of Cardiology Brazil., Markman M; Hospital Agamenon Magalhães, Department of Cardiology Brazil., Markman-Filho B; Hospital das Clínicas da UFPE, Department of Cardiology Brazil.
Publikováno v:
American journal of cardiovascular disease [Am J Cardiovasc Dis] 2018 Apr 05; Vol. 8 (2), pp. 19-23. Date of Electronic Publication: 2018 Apr 05 (Print Publication: 2018).