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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
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.
Optical flow driven interpolation for isotropic FIB-SEM reconstructions.
González-Ruiz V, García-Ortiz JP, Fernández-Fernández MR, Fernández JJ. González-Ruiz V, et al. Among authors: garcia ortiz jp. Comput Methods Programs Biomed. 2022 Jun;221:106856. doi: 10.1016/j.cmpb.2022.106856. Epub 2022 May 5. Comput Methods Programs Biomed. 2022. PMID: 35544963 Free article.
Clinical Exome Sequencing Enables Congenital Sialidosis Type II Diagnosis in Two Siblings Presenting with Unreported Clinical Features from a Rare Homozygous Sequence Variant p.(Tyr370Cys) in NEU1.
Flores-Contreras EA, García-Ortiz JE, Robles-Espinoza CD, Zomosa-Signoret V, Becerra-Solano LE, Vidaltamayo R, Castaneda-García C, Esparza-García E, Molina-Aguilar C, Hernández-Orozco AA, Córdova-Fletes C. Flores-Contreras EA, et al. Among authors: garcia ortiz je. Mol Syndromol. 2021 Jul;12(4):250-257. doi: 10.1159/000515081. Epub 2021 Jun 17. Mol Syndromol. 2021. PMID: 34421504 Free PMC article.
Prediction of Relapse After Anti-Tumor Necrosis Factor Cessation in Crohn's Disease: Individual Participant Data Meta-analysis of 1317 Patients From 14 Studies.
Pauwels RWM, van der Woude CJ, Nieboer D, Steyerberg EW, Casanova MJ, Gisbert JP, Kennedy NA, Lees CW, Louis E, Molnár T, Szántó K, Leo E, Bots S, Downey R, Lukas M, Lin WC, Amiot A, Lu C, Roblin X, Farkas K, Seidelin JB, Duijvestein M, D'Haens GR, de Vries AC; CEASE Study Group. Pauwels RWM, et al. Clin Gastroenterol Hepatol. 2022 Aug;20(8):1671-1686.e16. doi: 10.1016/j.cgh.2021.03.037. Epub 2021 Apr 30. Clin Gastroenterol Hepatol. 2022. PMID: 33933376 Free article. Review.
A clinical report of the massive CAG repeat expansion in spinocerebellar ataxia type 2: Severe onset in a Mexican child and review previous cases.
Sánchez-Corona J, Ramirez-Garcia SA, Castañeda-Cisneros G, Gutiérrez-Rubio SA, Volpini V, Sánchez-Garcia DM, García-Ortiz JE, García-Cruz D. Sánchez-Corona J, et al. Among authors: garcia ortiz je. Genet Mol Biol. 2020 Aug 21;43(3):e20190325. doi: 10.1590/1678-4685-gmb-2019-0325. Genet Mol Biol. 2020. PMID: 32870233 Free PMC article.
87 results