Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Rafael Nieto-García"'
Autor:
Pascuala B. Rivera-Ramírez, Juan C. Lona-Reyes, Jesse Jiménez-Bulnes, Rafael Nieto-García, Alejandro Barrón-Balderas, Magaly Valencia-Rodas
Publikováno v:
Archivos de Cardiología de México, Vol 93, Iss 96 (2023)
Externí odkaz:
https://doaj.org/article/a265939243cd44b6a021cbf7478f62f0
Autor:
Gerardo E. Fabián-Morales, Lucina Bobadilla-Morales, Christian Peña-Padilla, Rafael Nieto-García, Pascuala B. Rivera-Ramírez, Alfredo Corona-Rivera, Aurea Márquez-Mora, Graciela Macías-Salcedo, Idalid Cuero-Quezada, Jorge R. Corona-Rivera
Publikováno v:
Boletín Médico del Hospital Infantil de México, Vol 79, Iss 6 (2022)
Background: Congenital heart defects (CHD) are among the most frequent manifestations of 22q11.2 deletion syndrome. Although we found relatively few studies aimed at specifically detecting 22q11.2 deletion in newborns (NB) with CHD, none of them has
Externí odkaz:
https://doaj.org/article/dfc31b69b4044c08b4a126ab9777b5ef
Maternal risk factors for congenital heart defects in infants with Down syndrome from Western Mexico
Autor:
Alfredo Corona-Rivera, Gerardo E. Fabián‐Morales, Rafael Nieto-García, Andrea S. Gutiérrez‐Chávez, Jorge Román Corona-Rivera, Izabel Maryalexandra Rios-Flores, Cynthia Lugo‐Iglesias, Lucina Bobadilla-Morales, Ignacio Zavala‐Cortés, Christian Peña-Padilla
Publikováno v:
American Journal of Medical Genetics Part A.
Atrioventricular septal defects (AVSDs) have been identified as intriguingly infrequent among Hispanics with Down syndrome (DS) born in the United States. The aim of this study was to evaluate the effect of possible maternal risk factors in the prese
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38f0a8f0a827fe95f5f3870fcf271c37
https://doi.org/10.1002/ajmg.a.61300
https://doi.org/10.1002/ajmg.a.61300
Autor:
Lucina Bobadilla-Morales, Ana Karen Sandoval-Talamantes, Rene O. Pérez-Ramírez, Susana Solís-Ledezma, Larissa María Gómez-Ruiz, Eugenio Zapata-Aldana, Alfredo Corona-Rivera, Jorge Román Corona-Rivera, Estrella Lizbeth Mellín-Sánchez, Rafael Nieto-García, Juan José Cárdenas-Ruiz Velasco, Eloy López-Marure, Rafael L. Aguirre-Guillén
Publikováno v:
American Journal of Medical Genetics Part A. 170:316-321
The aim of our study was to determine the frequency and type of associated congenital anomalies in patients with isolated gastroschisis born at the Dr. Juan I. Menchaca Civil Hospital of Guadalajara (Guadalajara, México), and to explore its possible
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0bfefb667ebdf90daf73a03294b351be
https://doi.org/10.1002/ajmg.a.37433
https://doi.org/10.1002/ajmg.a.37433