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Page 1
Maternal Folic Acid Intake and Methylation Status of Genes Associated with Ventricular Septal Defects in Children: Case-Control Study.
González-Peña SM, Calvo-Anguiano G, Martínez-de-Villarreal LE, Ancer-Rodríguez PR, Lugo-Trampe JJ, Saldivar-Rodríguez D, Hernández-Almaguer MD, Calzada-Dávila M, Guerrero-Orjuela LS, Campos-Acevedo LD. González-Peña SM, et al. Among authors: martinez de villarreal le. Nutrients. 2021 Jun 17;13(6):2071. doi: 10.3390/nu13062071. Nutrients. 2021. PMID: 34204335 Free PMC article.
[Folic acid levels, homocysteine and polymorphism of methylenetetrahydrofolate reductase enzyme (MTHFR) in patients with pre-eclampsia and eclampsia].
Perales Dávila J, Martínez de Villarreal LE, Triana Saldaña H, Saldívar Rodríguez D, Barrera Saldaña H, Rojas Martínez A, López Valdez R, Garza Elizondo M, García Cavazos R, Valdez Leal R, Zacarías Villarreal Pérez J. Perales Dávila J, et al. Ginecol Obstet Mex. 2001 Jan;69:6-11. Ginecol Obstet Mex. 2001. PMID: 11268732 Spanish.
Folate levels and N(5),N(10)-methylenetetrahydrofolate reductase genotype (MTHFR) in mothers of offspring with neural tube defects: a case-control study.
Martínez de Villarreal LE, Delgado-Enciso I, Valdéz-Leal R, Ortíz-López R, Rojas-Martínez A, Limón-Benavides C, Sánchez-Peña MA, Ancer-Rodríguez J, Barrera-Saldaña HA, Villarreal-Pérez JZ. Martínez de Villarreal LE, et al. Arch Med Res. 2001 Jul-Aug;32(4):277-82. doi: 10.1016/s0188-4409(01)00292-2. Arch Med Res. 2001. PMID: 11440783
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
Bloom syndrome sans characteristic facial features in a Mestizo patient- a diagnostic challenge.
Chavez-Alvarez S, Villarreal-Martinez A, Velasco-Campos MDR, Moreno-Vega I, Martinez-de-Villarreal LE, Herz-Ruelas M, Ocampo-Candiani J, Campos-Acevedo LD. Chavez-Alvarez S, et al. Indian J Dermatol Venereol Leprol. 2019 Jan-Feb;85(1):130. doi: 10.4103/ijdvl.IJDVL_787_16. Indian J Dermatol Venereol Leprol. 2019. PMID: 29794356 Free article. No abstract available.
Bioinformatic Analysis of Gene Variants from Gastroschisis Recurrence Identifies Multiple Novel Pathogenetic Pathways: Implication for the Closure of the Ventral Body Wall.
Salinas-Torres VM, Gallardo-Blanco HL, Salinas-Torres RA, Cerda-Flores RM, Lugo-Trampe JJ, Villarreal-Martínez DZ, Martínez de Villarreal LE. Salinas-Torres VM, et al. Int J Mol Sci. 2019 May 9;20(9):2295. doi: 10.3390/ijms20092295. Int J Mol Sci. 2019. PMID: 31075877 Free PMC article.
57 results