Fachal L - Search Results

1

Investigating the role of mitochondrial haplogroups in genetic predisposition to meningococcal disease.

Salas A, Fachal L, Marcos-Alonso S, Vega A, Martinón-Torres F; Grupo de investigación ESIGEM (Estudio Sobre la Influencia Genética en la Enfermedad Meningocócica). Salas A, et al. Among authors: fachal l. PLoS One. 2009 Dec 17;4(12):e8347. doi: 10.1371/journal.pone.0008347. PLoS One. 2009. PMID: 20019817 Free PMC article.

2

BRCA1 mutations do not increase prostate cancer risk: results from a meta-analysis including new data.

Fachal L, Gómez-Caamaño A, Celeiro-Muñoz C, Peleteiro P, Blanco A, Carballo A, Forteza J, Carracedo A, Vega A. Fachal L, et al. Prostate. 2011 Dec;71(16):1768-79. doi: 10.1002/pros.21394. Epub 2011 Apr 25. Prostate. 2011. PMID: 21520156

3

Analysis of TGM1, ALOX12B, ALOXE3, NIPAL4 and CYP4F22 in autosomal recessive congenital ichthyosis from Galicia (NW Spain): evidence of founder effects.

Rodríguez-Pazos L, Ginarte M, Fachal L, Toribio J, Carracedo A, Vega A. Rodríguez-Pazos L, et al. Among authors: fachal l. Br J Dermatol. 2011 Oct;165(4):906-11. doi: 10.1111/j.1365-2133.2011.10454.x. Epub 2011 Aug 4. Br J Dermatol. 2011. PMID: 21668430

4

TGFβ1 SNPs and radio-induced toxicity in prostate cancer patients.

Fachal L, Gómez-Caamaño A, Sánchez-García M, Carballo A, Peleteiro P, Lobato-Busto R, Carracedo A, Vega A. Fachal L, et al. Radiother Oncol. 2012 May;103(2):206-9. doi: 10.1016/j.radonc.2012.01.015. Epub 2012 Mar 3. Radiother Oncol. 2012. PMID: 22385796

5

Characterization of TGM1 c.984+1G>A mutation identified in a homozygous carrier of lamellar ichthyosis.

Fachal L, Rodríguez-Pazos L, Ginarte M, Beiras A, Suárez-Peñaranda JM, Toribio J, Carracedo Á, Vega A. Fachal L, et al. Int J Dermatol. 2012 Apr;51(4):427-30. doi: 10.1111/j.1365-4632.2011.05171.x. Int J Dermatol. 2012. PMID: 22435431

6

Multiple local and recent founder effects of TGM1 in Spanish families.

Fachal L, Rodríguez-Pazos L, Ginarte M, Toribio J, Salas A, Vega A. Fachal L, et al. PLoS One. 2012;7(4):e33580. doi: 10.1371/journal.pone.0033580. Epub 2012 Apr 12. PLoS One. 2012. PMID: 22511925 Free PMC article.

7

Association of a XRCC3 polymorphism and rectum mean dose with the risk of acute radio-induced gastrointestinal toxicity in prostate cancer patients.

Fachal L, Gómez-Caamaño A, Peleteiro P, Carballo A, Calvo-Crespo P, Sánchez-García M, Lobato-Busto R, Carracedo A, Vega A. Fachal L, et al. Radiother Oncol. 2012 Dec;105(3):321-8. doi: 10.1016/j.radonc.2012.09.013. Epub 2012 Oct 15. Radiother Oncol. 2012. PMID: 23075580

8

CHEK2 c.1100delC mutation among non-BRCA1/2 Spanish hereditary breast cancer families.

Fachal L, Santamariña M, Blanco A, Carracedo A, Vega A. Fachal L, et al. Clin Transl Oncol. 2013 Feb;15(2):164-5. doi: 10.1007/s12094-012-0967-z. Epub 2012 Nov 13. Clin Transl Oncol. 2013. PMID: 23150219 No abstract available.

9

Indian signatures in the westernmost edge of the European Romani diaspora: new insight from mitogenomes.

Gómez-Carballa A, Pardo-Seco J, Fachal L, Vega A, Cebey M, Martinón-Torres N, Martinón-Torres F, Salas A. Gómez-Carballa A, et al. Among authors: fachal l. PLoS One. 2013 Oct 15;8(10):e75397. doi: 10.1371/journal.pone.0075397. eCollection 2013. PLoS One. 2013. PMID: 24143169 Free PMC article.

10

Identification of a novel PNPLA1 mutation in a Spanish family with autosomal recessive congenital ichthyosis.

Fachal L, Rodríguez-Pazos L, Ginarte M, Carracedo A, Toribio J, Vega A. Fachal L, et al. Br J Dermatol. 2014 Apr;170(4):980-2. doi: 10.1111/bjd.12757. Br J Dermatol. 2014. PMID: 24344921 No abstract available.

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