Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Diana I. Hernández Zaragoza"'
Autor:
Janette Furuzawa-Carballeda, Joaquín Zuñiga, Diana I Hernández-Zaragoza, Rodrigo Barquera, Eduardo Marques-García, Luis Jiménez-Alvarez, Alfredo Cruz-Lagunas, Gustavo Ramírez, Nora E Regino, Ramón Espinosa-Soto, Edmond J Yunis, Fernanda Romero-Hernández, Daniel Azamar-Llamas, Enrique Coss-Adame, Miguel A Valdovinos, Samuel Torres-Landa, Axel Palacios-Ramírez, Blanca Breña, Edgar Alejandro-Medrano, Axel Hernández-Ávila, Julio Granados, Gonzalo Torres-Villalobos
Publikováno v:
PLoS ONE, Vol 13, Iss 8, p e0201676 (2018)
Idiopathic achalasia is a relatively infrequent esophageal motor disorder for which major histocompatibility complex (MHC) genes are well-identified risk factors. However, no information about HLA-achalasia susceptibility in Mexicans has previously b
Externí odkaz:
https://doaj.org/article/14716e5a6831495db68b3cc5444c1439
Autor:
Juan M. Galarza, Mariel Pérez, Johannes Krause, Andrea Tamayo, Gabriela Peralta Sevilla, David Dávila, Ana M. Tito Álvarez, Marcelo Grijalva, Diana I. Hernández Zaragoza, Lotty Birnberg, Rodrigo Barquera, Víctor Acuña Alonzo
Publikováno v:
Human Immunology. 79:639-650
We studied HLA class I (HLA-A, -B) and class II (HLA-DRB1, -DQB1) alleles by PCR-SSP based typing in a total of 1101 Ecuadorian individuals from three regions of the country, the Coastal region, the Andean region, and the Amazonian region, to obtain
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2af70409c406f5272f64276059125c68
https://doi.org/10.1016/j.humimm.2018.06.004
https://doi.org/10.1016/j.humimm.2018.06.004
Autor:
Gonzalo Torres-Villalobos, Daniel Azamar-Llamas, Edgar Alejandro-Medrano, Diana I. Hernández Zaragoza, Samuel Torres-Landa, Julio Granados, Ramon Espinoza-Soto, Luis Jiménez-Alvarez, Blanca A. Blancas Breña, Edmond J. Yunis, Joaquín Zúñiga, Axel A. Hernández-Ávila, Eduardo Marques-García, Rodrigo Barquera, Alfredo Cruz-Lagunas, Nora E. Regino, Miguel A. Valdovinos, Axel Palacios-Ramírez, Enrique Coss-Adame, Fernanda Romero-Hernández, Janette Furuzawa-Carballeda
Publikováno v:
Gastroenterology. 154:S-736
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9565aa5dcbc27e581fd188da76f2eae4
https://doi.org/10.1016/s0016-5085(18)32564-2
https://doi.org/10.1016/s0016-5085(18)32564-2
Autor:
Damián Palafox, Claudia Gutiérrez-Gómez, Julio Granados, Rodrigo Barquera, Esteban Ortega-Hernández, Diana I. Hernández-Zaragoza, Marcia Pérez-Dosal, Hanna R. Pacheco-Ubaldo, Abraham Lona-Sánchez
Publikováno v:
Cirugía Plástica Ibero-Latinoamericana, Vol 42, Iss 2, Pp 115-120
Introducción y Objetivo. El síndrome de Parry Romberg se caracteriza por atrofia hemifacial progresiva; afecta piel y tejidos blandos y en ocasiones provoca también atrofia de músculos, cartílago y estructuras óseas subyacentes. Su diagnóstico
Externí odkaz:
https://doaj.org/article/c75e399477b1437d834724ef8dbb7d18