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Page 1
Pharmacogenetics: ethnicity, treatment and health in Latin American populations.
Sosa-Macías M, Fricke-Galindo I, Fariñas H, Monterde L, Ruiz-Cruz ED, Molina-Guarneros J, Tarazona-Santos E, Rodrigues-Soares F, Galaviz-Hernández C, Peñas-Lledó E, Moya G, Lara-Riegos J, Terán E, Hernández I, Ramírez-Roa R, Altamirano-Tinoco C, López-López M, García-Ortiz JE, LLerena A. Sosa-Macías M, et al. Among authors: garcia ortiz je. Pharmacogenomics. 2023 Jun;24(9):489-492. doi: 10.2217/pgs-2023-0098. Epub 2023 Aug 2. Pharmacogenomics. 2023. PMID: 37529900
Second female case of Myhre syndrome.
Lopez-Cardona MG, Garcia-Cruz D, Garcia-Ortiz JE, Davalos NO, Feria-Velasco A, Rodriguez-Rojas LX, Garcia-Cruz MO, Figuera-Villanueva LE, Stephens A, Larios-Arceo F, Sanchez-Corona J. Lopez-Cardona MG, et al. Clin Dysmorphol. 2004 Apr;13(2):91-94. Clin Dysmorphol. 2004. PMID: 15057124
Apolipoprotein E genotypes in Mexican patients with Parkinson's disease.
Gallegos-Arreola MP, Figuera LE, Ortiz GG, Jiménez-Gil FJ, Ramírez-Vega J, Ruíz-Sandoval JL, Puebla-Pérez AM, Troyo-Sanroman R, García-Ortiz JE, Sanchez-Corona J, Zúñiga-González GM. Gallegos-Arreola MP, et al. Dis Markers. 2009;27(5):225-30. doi: 10.3233/DMA-2009-0667. Dis Markers. 2009. PMID: 20037210 Free PMC article.
The association between the 844ins68 polymorphism in the CBS gene and breast cancer.
Gallegos-Arreola MP, Figuera-Villanueva LE, Ramos-Silva A, Salas-González E, Puebla-Pérez AM, Peralta-Leal V, García-Ortiz JE, Dávalos-Rodríguez IP, Zúñiga-González GM. Gallegos-Arreola MP, et al. Arch Med Sci. 2014 Dec 22;10(6):1214-24. doi: 10.5114/aoms.2014.47830. Arch Med Sci. 2014. PMID: 25624861 Free PMC article.
Biochemical diagnosis of mucopolysaccharidosis in a Mexican reference center.
Mendoza-Ruvalcaba SDC, Brambila-Tapia AJL, Juárez-Osuna JA, Silva-José TDD, García-Ortiz JE. Mendoza-Ruvalcaba SDC, et al. Genet Mol Biol. 2020 Feb 14;43(1):e20180347. doi: 10.1590/1678-4685-GMB-2018-0347. eCollection 2020. Genet Mol Biol. 2020. PMID: 32106281 Free PMC article.
Mutational spectrum of the iduronate-2-sulfatase gene in Mexican patients with Hunter syndrome.
Ramírez-Hernández MA, Figuera LE, Rizo-de la Torre LC, Mendoza-Ruvalcaba MTMSC, Arnaud-López L, García-Ortiz JE, Zúñiga-González GM, Puebla-Pérez AM, Gómez-Meda BC, Gallegos-Arreola MP. Ramírez-Hernández MA, et al. Among authors: garcia ortiz je. Eur Rev Med Pharmacol Sci. 2022 Jul;26(14):5115-5127. doi: 10.26355/eurrev_202207_29300. Eur Rev Med Pharmacol Sci. 2022. PMID: 35916809 Free article.
Mexican consensus on lysosomal acid lipase deficiency diagnosis.
Vázquez-Frias R, García-Ortiz JE, Valencia-Mayoral PF, Castro-Narro GE, Medina-Bravo PG, Santillán-Hernández Y, Flores-Calderón J, Mehta R, Arellano-Valdés CA, Carbajal-Rodríguez L, Navarrete-Martínez JI, Urbán-Reyes ML, Valadez-Reyes MT, Zárate-Mondragón F, Consuelo-Sánchez A. Vázquez-Frias R, et al. Rev Gastroenterol Mex (Engl Ed). 2018 Jan-Mar;83(1):51-61. doi: 10.1016/j.rgmx.2017.08.001. Epub 2017 Dec 27. Rev Gastroenterol Mex (Engl Ed). 2018. PMID: 29287906 Free article. English, Spanish.
63 results