Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Juana Inés Navarrete Martínez"'
Publikováno v:
Acta Pediátrica de México, Vol 36, Iss 5, Pp 369-373 (2015)
El concepto de enfermedades “raras” se acuñó por primera vez a mediados de la década de los años 80 del siglo pasado, en Estados Unidos, relacionado con el concepto de medicamentos “huérfanos”.
Externí odkaz:
https://doaj.org/article/416d58b2a60f4d4dba57a9130cd07564
Autor:
Nydia Avila-Vazzini, Mayra Domínguez-Pérez, Enrique López-Mora, Rigoberto Rosendo-Gutiérrez, Fernando Pérez-Villatoro, Leonor Jacobo-Albavera, Gilberto Vargas-Alarcón, Alessandra Carnevale, Juana Inés Navarrete-Martínez, Sandra Rosas-Madrigal, María Teresa Villarreal-Molina, Sandra Romero-Hidalgo
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 8, Iss 11, Pp n/a-n/a (2020)
Molecular Genetics & Genomic Medicine, Vol 8, Iss 11, Pp n/a-n/a (2020)
Background Dilated cardiomyopathy (DCM) is a major cause of nonischemic heart failure and death in young adults. Next generation sequencing (NGS) has become part of the diagnostic workup in idiopathic and familial DCM. More than 50 DCM genes have bee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31776441bc1d58257226d7ca269af06a
https://pubmed.ncbi.nlm.nih.gov/32969603
https://pubmed.ncbi.nlm.nih.gov/32969603
Autor:
Consuelo Cantú-Reyna, Ma. del Rocío Delgado-Calvillo, David E. Cervantes-Barragán, Juana Inés Navarrete-Martínez, Ana Elena Limón-Rojas, Jesús Reyna-Figueroa, Maria de Jesús Gaytán-García, Héctor Cruz-Camino, Guillermo Wakida-Kusunoki
Publikováno v:
Molecular genetics and metabolism. 121(1)
Objective To evaluate the results of a lysosomal newborn screening (NBS) program in a cohort of 20,018 Mexican patients over the course of 3 years in a closed Mexican Health System (Petroleos Mexicanos [PEMEX] Health Services). Study design Using dri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80bd79180a43dee6c81bd00314ad6d76
https://pubmed.ncbi.nlm.nih.gov/28302345
https://pubmed.ncbi.nlm.nih.gov/28302345
Autor:
Alessandra Carnevale, Sandra Rosas‐Madrigal, Rigoberto Rosendo‐Gutiérrez, Enrique López‐Mora, Sandra Romero‐Hidalgo, Nydia Avila‐Vazzini, Leonor Jacobo‐Albavera, Mayra Domínguez‐Pérez, Gilberto Vargas‐Alarcón, Fernando Pérez‐Villatoro, Juana Inés Navarrete‐Martínez, María Teresa Villarreal–Molina
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 11, Pp n/a-n/a (2020)
Abstract Background Dilated cardiomyopathy (DCM) is a major cause of nonischemic heart failure and death in young adults. Next generation sequencing (NGS) has become part of the diagnostic workup in idiopathic and familial DCM. More than 50 DCM genes
Externí odkaz:
https://doaj.org/article/599d186982a54fa1bc443a52769359ef