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Page 1
Hypospadias Prevalence and Trends in International Birth Defect Surveillance Systems, 1980-2010.
Yu X, Nassar N, Mastroiacovo P, Canfield M, Groisman B, Bermejo-Sánchez E, Ritvanen A, Kiuru-Kuhlefelt S, Benavides A, Sipek A, Pierini A, Bianchi F, Källén K, Gatt M, Morgan M, Tucker D, Canessa MA, Gajardo R, Mutchinick OM, Szabova E, Csáky-Szunyogh M, Tagliabue G, Cragan JD, Nembhard WN, Rissmann A, Goetz D, Bower C, Baynam G, Lowry RB, Leon JA, Luo W, Rouleau J, Zarante I, Fernandez N, Amar E, Dastgiri S, Contiero P, Martínez-de-Villarreal LE, Borman B, Bergman JEH, de Walle HEK, Hobbs CA, Nance AE, Agopian AJ. Yu X, et al. Eur Urol. 2019 Oct;76(4):482-490. doi: 10.1016/j.eururo.2019.06.027. Epub 2019 Jul 9. Eur Urol. 2019. PMID: 31300237 Free PMC article.
Decline of neural tube defects cases after a folic acid campaign in Nuevo León, México.
Martínez de Villarreal L, Pérez JZ, Vázquez PA, Herrera RH, Campos Mdel R, López RA, Ramírez JL, Sánchez JM, Villarreal JJ, Garza MT, Limón A, López AG, Bárcenas M, García JR, Domínguez AS, Nuñez RH, Ayala JL, Martínez JG, González MT, Alvarez CG, Castro RN. Martínez de Villarreal L, et al. Teratology. 2002 Nov;66(5):249-56. doi: 10.1002/tera.10094. Teratology. 2002. PMID: 12397633
Proteomic profile of preeclampsia in the first trimester of pregnancy.
Jacobo-Baca G, Salazar-Ybarra RA, Torres-de-la-Cruz V, Guzmán-López S, Elizondo-Omaña RE, Guzmán-López A, Vázquez-Barragán MÁ, Martínez-de-Villarreal LE. Jacobo-Baca G, et al. Among authors: martinez de villarreal le. J Matern Fetal Neonatal Med. 2022 Sep;35(18):3446-3452. doi: 10.1080/14767058.2020.1820980. Epub 2020 Sep 21. J Matern Fetal Neonatal Med. 2022. PMID: 32957816
GJB2 and GJB6 mutations are an infrequent cause of autosomal-recessive nonsyndromic hearing loss in residents of Mexico.
Hernández-Juárez AA, Lugo-Trampe Jde J, Campos-Acevedo LD, Lugo-Trampe A, Treviño-González JL, de-la-Cruz-Ávila I, Martínez-de-Villarreal LE. Hernández-Juárez AA, et al. Int J Pediatr Otorhinolaryngol. 2014 Dec;78(12):2107-12. doi: 10.1016/j.ijporl.2014.09.016. Epub 2014 Sep 28. Int J Pediatr Otorhinolaryngol. 2014. PMID: 25288386
Detection of Turner Syndrome by quantitative PCR of SHOX and VAMP7 genes.
Ibarra-Ramírez M, Zamudio-Osuna MJ, Campos-Acevedo LD, Gallardo-Blanco HL, Cerda-Flores RM, Rodríguez-Sánchez IP, Martínez-de-Villarreal LE. Ibarra-Ramírez M, et al. Genet Test Mol Biomarkers. 2015 Feb;19(2):88-92. doi: 10.1089/gtmb.2014.0236. Epub 2014 Dec 23. Genet Test Mol Biomarkers. 2015. PMID: 25535777
Identification of novel mutations in Mexican patients with Aarskog-Scott syndrome.
Pérez-Coria M, Lugo-Trampe JJ, Zamudio-Osuna M, Rodríguez-Sánchez IP, Lugo-Trampe A, de la Fuente-Cortez B, Campos-Acevedo LD, Martínez-de-Villarreal LE. Pérez-Coria M, et al. Mol Genet Genomic Med. 2015 May;3(3):197-202. doi: 10.1002/mgg3.132. Epub 2015 Feb 17. Mol Genet Genomic Med. 2015. PMID: 26029706 Free PMC article.
Dosage of Sex Chromosomal Genes in Blood Deposited on Filter Paper for Neonatal Screening of Sex Chromosome Aneuploidy.
Campos-Acevedo LD, Ibarra-Ramirez M, de Jesús Lugo-Trampe J, de Jesús Zamudio-Osuna M, Torres-Muñoz I, Del Roble Velasco-Campos M, Rojas-Patlan L, Rodríguez-Sánchez IP, Martínez-de-Villarreal LE. Campos-Acevedo LD, et al. Genet Test Mol Biomarkers. 2016 Dec;20(12):786-790. doi: 10.1089/gtmb.2016.0101. Epub 2016 Oct 19. Genet Test Mol Biomarkers. 2016. PMID: 27997249
55 results