Search Results - Gallardo Blanco, Hugo Leonid
- Showing 1 - 13 results of 13
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Association study in mexican patients with thyrotoxic hypokalemic periodic paralysis by Bautista Medina, Mario Arturo, Gallardo Blanco, Hugo Leonid, Martínez Garza, Laura Elia, Cerda Flores, Ricardo Martín, Lavalle González, Fernando Javier, Villarreal Pérez, Jesús Zacarías
Published 2020
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Detection of Turner Syndrome by Quantitative PCR of SHOX and VAMP7 Genes by Ibarra Ramírez, Marisol, Zamudio Osuna, Michelle de Jesús, Campos Acevedo, Luis Daniel, Gallardo Blanco, Hugo Leonid, Cerda Flores, Ricardo Martín, Rodríguez Sánchez, Irám Pablo, Martínez de Villarreal, Laura Elia
Published 2015
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A pharmacogenetic pilot study reveals MTHFR, DRD3, and MDR1 polymorphisms as biomarker candidates for slow atorvastatin metabolizers by León Cachón, Rafael B. R., Ascacio Martínez, Jorge Ángel Isidro, Gamino Peña, María E., Cerda Flores, Ricardo Martín, Meester, Irene, Gallardo Blanco, Hugo Leonid, Gómez Silva, Magdalena, Piñeyro Garza, Everardo, Barrera Saldaña, Hugo Alberto
Published 2016
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The tumor necrosis factor α (-308 A/G) polymorphism is associated with cystic fibrosis in Mexican patients by Sánchez Domínguez, Celia Nohemí, Reyes López, Miguel A., Bustamante, Adriana, Cerda Flores, Ricardo Martín, Villalobos Torres, María del Carmen, Gallardo Blanco, Hugo Leonid, Rojas Martínez, Augusto, Martínez Rodríguez, Herminia Guadalupe, Barrera Saldaña, Hugo Alberto, Ortiz López, Rocío
Published 2014
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Genetic variants in KCNJ11, TCF7L2 and HNF4A are associated with type 2 diabetes, BMI and dyslipidemia in families of Northeastern Mexico: A pilot study by Gallardo Blanco, Hugo Leonid, Villarreal Pérez, Jesús Zacarías, Cerda Flores, Ricardo Martín, Figueroa, Andres, Sánchez Domínguez, Celia Nohemí, Gutiérrez Valverde, Juana Mercedes, Torres Muñoz, Iris Carmen, Lavalle González, Fernando Javier, Gallegos Cabriales, Esther Carlota, Martínez Garza, Laura Elia
Published 2016
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