Zobrazeno 1 - 10 of 49 pro vyhledávání: '"Davanzo, M."'
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[Improvement of prognosis in idiopathic dilated cardiomyopathy: role of early diagnosis and optimized medical treatment. Study Group on Heart Muscle Diseases]
Autor: Di Lenarda, A, Hlede, S, Sabbadini, Gastone, Davanzo, M, Di Chiara, C, Scherl, G, Zanchi, C, Sinagra, Gianfranco
Publikováno v: Giornale italiano di cardiologia. 29(12)
The aim of this study was to assess the extent to which a more widespread use of new effective treatments for heart failure associated with earlier detection of the disease may have contributed to enhancing the prognosis of idiopathic dilated cardiom
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::3ed86ca9d8a9787c4dc858c6fad63e37
https://pubmed.ncbi.nlm.nih.gov/10687108
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7
A point mutation in the 5' splice site of the dystrophin gene first intron responsible for X-linked dilated cardiomyopathy
Autor: Milasin, J., Muntoni, F., Severini, G. M., Bartoloni, L., Vatta, M., Krajinovic, M., Mateddu, A., Angelini, C., Camerini, F., Falaschi, A., Mestroni, L., MAURO GIACCA, Pinamonti, B., Sinagra, G., Di Lenarda, A., Silvestri, F., Bussani, R., Davanzo, M.
Publikováno v: Scopus-Elsevier
Human Molecular Genetics
X-linked dilated cardiomyopathy (XLDC) is a familial heart disease presenting in young males as a rapidly progressive congestive heart failure, without clinical signs of skeletal myopathy. This condition has recently been linked to the dystrophin gen
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::245288808fecbeb3eabe1b92642c04b6
https://pubmed.ncbi.nlm.nih.gov/8789442
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Plný text Recenzováno Digitální knihovna AV ČR
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