Figuera LE - Search Results

1

Mutation of SDHB is a cause of hypoxia-related high-altitude paraganglioma.

Cerecer-Gil NY, Figuera LE, Llamas FJ, Lara M, Escamilla JG, Ramos R, Estrada G, Hussain AK, Gaal J, Korpershoek E, de Krijger RR, Dinjens WN, Devilee P, Bayley JP. Cerecer-Gil NY, et al. Among authors: figuera le. Clin Cancer Res. 2010 Aug 15;16(16):4148-54. doi: 10.1158/1078-0432.CCR-10-0637. Epub 2010 Jun 30. Clin Cancer Res. 2010. PMID: 20592014

2

Association of the 677C -->T polymorphism in the MTHFR gene with colorectal cancer in Mexican patients.

Gallegos-Arreola MP, García-Ortiz JE, Figuera LE, Puebla-Pérez AM, Morgan-Villela G, Zúñiga-González GM. Gallegos-Arreola MP, et al. Among authors: figuera le. Cancer Genomics Proteomics. 2009 May-Jun;6(3):183-8. Cancer Genomics Proteomics. 2009. PMID: 19487547 Free article.

3

Inherited hypertrichoses.

Garcia-Cruz D, Figuera LE, Cantu JM. Garcia-Cruz D, et al. Among authors: figuera le. Clin Genet. 2002 May;61(5):321-9. doi: 10.1034/j.1399-0004.2002.610501.x. Clin Genet. 2002. PMID: 12081714 Review.

4

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. Among authors: figuera le. Dis Markers. 2009;27(5):225-30. doi: 10.3233/DMA-2009-0667. Dis Markers. 2009. PMID: 20037210 Free PMC article.

5

The TP53 16-bp duplication polymorphism is enriched in endometriosis patients.

Gallegos-Arreola MP, Valencia-Rodríguez LE, Puebla-Pérez AM, Figuera LE, Zúñiga-González GM. Gallegos-Arreola MP, et al. Among authors: figuera le. Gynecol Obstet Invest. 2012;73(2):118-23. doi: 10.1159/000330702. Epub 2012 Feb 17. Gynecol Obstet Invest. 2012. PMID: 22353881

6

Determination of SCN1A genetic variants in Mexican patients with refractory epilepsy and Dravet syndrome.

Jiménez-Arredondo RE, Brambila-Tapia AJL, Mercado-Silva FM, Magaña-Torres MT, Figuera LE. Jiménez-Arredondo RE, et al. Among authors: figuera le. Genet Mol Res. 2017 May 18;16(2). doi: 10.4238/gmr16029405. Genet Mol Res. 2017. PMID: 28525652 Free article.

7

Guadalajara camptodactyly syndrome type I. A corroborative family.

Figuera LE, Ramírez-Dueñas ML, García-Cruz D, Villar V, Cantú JM. Figuera LE, et al. Clin Genet. 1993 Jan;43(1):11-5. doi: 10.1111/j.1399-0004.1993.tb04418.x. Clin Genet. 1993. PMID: 7681735

8

Ambiguous genitalia by 9p deletion inherent to a dic(Y;9)(q12;p24).

Vásquez-Velásquez AI, Arnaud-López L, Figuera LE, Padilla-Gutiérrez JR, Rivas F, Rivera H. Vásquez-Velásquez AI, et al. Among authors: figuera le. J Appl Genet. 2005;46(4):415-8. J Appl Genet. 2005. PMID: 16278517

9

Association between polymorphisms of the androgen and vitamin D receptor genes with prostate cancer risk in a Mexican population.

Patiño-García B, Arroyo C, Rangel-Villalobos H, Soto-Vega E, Velarde-Félix JS, Gabilondo F, Sandoval-Ramirez L, Figuera LE. Patiño-García B, et al. Among authors: figuera le. Rev Invest Clin. 2007 Jan-Feb;59(1):25-31. Rev Invest Clin. 2007. PMID: 17569297

10

Distribution of CYP1A1*2A polymorphism in adult patients with acute lymphoblastic leukemia in a Mexican population.

Gallegos-Arreola MP, González-García JR, Figuera LE, Puebla-Pérez AM, Delgado-Lamas JL, Zúñiga-González GM. Gallegos-Arreola MP, et al. Among authors: figuera le. Blood Cells Mol Dis. 2008 Jul-Aug;41(1):91-4. doi: 10.1016/j.bcmd.2007.12.001. Epub 2008 Jan 18. Blood Cells Mol Dis. 2008. PMID: 18203634

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