Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Arsonval Lamounier Júnior"'
Autor:
Arsonval Lamounier Júnior, Filipe Ferrari, Renato Max, Luiz Eduardo Fonteles Ritt, Ricardo Stein
Publikováno v:
Arquivos Brasileiros de Cardiologia, Vol 113, Iss 2, Pp 274-281
Abstract Dilated cardiomyopathy (DCM) is a clinical syndrome characterized by left ventricular dilatation and contractile dysfunction. It is the most common cause of heart failure in young adults. The advent of next-generation sequencing has contribu
Externí odkaz:
https://doaj.org/article/a30fc85998a24e90a4e7b33e3e2dd765
Autor:
Ricardo Stein, Juan Pablo Trujillo, Anderson Donelli da Silveira, Arsonval Lamounier Júnior, Lorenzo Monserrat Iglesias
Publikováno v:
Arquivos Brasileiros de Cardiologia, Iss 0
Externí odkaz:
https://doaj.org/article/da8a7a9a42844840b7f55d5a0e3d45b5
Autor:
Arsonval Lamounier Júnior
Publikováno v:
Amyloidosis and Fabry Disease ISBN: 9783031177583
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c9148163fc714a14582d6f60e1b49ba3
https://doi.org/10.1007/978-3-031-17759-0_30
https://doi.org/10.1007/978-3-031-17759-0_30
Autor:
Enrique Medina-Acosta, Daniel Barr, Fernando Eugênio dos Santos Cruz Filho, Antonio Carlos Carvalho, Glauber Monteiro Dias, Arsonval Lamounier Júnior, Eduardo Back Sternick, Maila Seifert, Hector Barajas-Martinez
Publikováno v:
Circulation: Genomic and Precision Medicine. 14
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d23400f0b7256c98dc3c9c4ebaa5b810
https://doi.org/10.1161/circgen.121.003476
https://doi.org/10.1161/circgen.121.003476
Autor:
Mario Torrado, Emilia Maneiro, Arsonval Lamounier Junior, Miguel Fernández-Burriel, Sara Sánchez Giralt, Ana Martínez-Carapeto, Laura Cazón, Elisa Santiago, Juan Pablo Ochoa, William J. McKenna, Luis Santomé, Lorenzo Monserrat
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-22 (2022)
Abstract The finding of a genotype-negative hypertrophic cardiomyopathy (HCM) pedigree with several affected members indicating a familial origin of the disease has driven this study to discover causative gene variants. Genetic testing of the proband
Externí odkaz:
https://doaj.org/article/c868467e243b4073b28e6489e0a7d28c