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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
A novel HLA-A allele: A*0257.
García-Ortiz JE, Cox ST, Sandoval-Ramirez L, Little AM, Marsh SG, Madrigal JA, Argüello JR. García-Ortiz JE, et al. Tissue Antigens. 2004 Jan;63(1):85-7. doi: 10.1111/j.1399-0039.2004.00154.x. Tissue Antigens. 2004. PMID: 14651529
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.
Dup-24 bp in the CHIT1 Gene in Six Mexican Amerindian Populations.
Da Silva-José TD, Juárez-Rendón KJ, Juárez-Osuna JA, Porras-Dorantes A, Valladares-Salgado A, Cruz M, Gonzalez-Ibarra M, Soto AG, Magaña-Torres MT, Sandoval-Ramírez L, García-Ortiz JE. Da Silva-José TD, et al. JIMD Rep. 2015;23:123-7. doi: 10.1007/8904_2015_442. Epub 2015 May 13. JIMD Rep. 2015. PMID: 25967229 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.
Severe Craniofacial Involvement due to Amniotic Band Sequence.
Becerra-Solano LE, Castañeda-Cisneros G, Corona-Rivera JR, Díaz-Rodríguez M, Figuera LE, López-Muñoz E, Nastasi-Catanese JA, Toscano-Flores JJ, Ramírez-Dueñas ML, García-Ortíz JE. Becerra-Solano LE, et al. Fetal Pediatr Pathol. 2018 Feb;37(1):27-37. doi: 10.1080/15513815.2017.1392663. Epub 2018 Jan 16. Fetal Pediatr Pathol. 2018. PMID: 29336649
Williams-Beuren syndrome in Mexican patients confirmed by FISH and assessed by aCGH.
Ramírez-Velazco A, Aguayo-Orozco TA, Figuera L, Rivera H, Jave-Suárez L, Aguilar-Lemarroy A, Torres-Reyes LA, Córdova-Fletes C, Barros-Núñez P, Delgadillo-Pérez S, Dávalos-Rodríguez IP, García-Ortiz JE, Domínguez MG. Ramírez-Velazco A, et al. J Genet. 2019 Jun;98(2):34. J Genet. 2019. PMID: 31204697 Free article.
63 results