Figuera LE - Search Results

1

Effects of enzyme replacement therapy in Fabry disease--a comprehensive review of the medical literature.

Lidove O, West ML, Pintos-Morell G, Reisin R, Nicholls K, Figuera LE, Parini R, Carvalho LR, Kampmann C, Pastores GM, Mehta A. Lidove O, et al. Among authors: figuera le. Genet Med. 2010 Nov;12(11):668-79. doi: 10.1097/GIM.0b013e3181f13b75. Genet Med. 2010. PMID: 20962662 Free article. Review.

2

Therapeutic goals in the treatment of Fabry disease.

Mehta A, West ML, Pintos-Morell G, Reisin R, Nicholls K, Figuera LE, Parini R, Carvalho LR, Kampmann C, Pastores GM, Lidove O. Mehta A, et al. Among authors: figuera le. Genet Med. 2010 Nov;12(11):713-20. doi: 10.1097/GIM.0b013e3181f6e676. Genet Med. 2010. PMID: 20975569 Free article.

3

Mutational analysis of the GLA gene in Mexican families with Fabry disease.

Gutiérrez-Amavizca BE, Gal A, Ortíz-Orozco R, Orth U, Prado Montes De Oca E, Gutiérrez-Amavizca JP, Figuera LE. Gutiérrez-Amavizca BE, et al. Among authors: figuera le. J Genet. 2017 Mar;96(1):161-164. doi: 10.1007/s12041-017-0744-4. J Genet. 2017. PMID: 28360401 Free article.

4

[Ophthalmic manifestations in Mexican patients with Fabry disease].

Beltrán-Becerra KJ, Ríos-González BE, Gutiérrez-Amavizca BE, Silva-Noriega DA, Figuera LE. Beltrán-Becerra KJ, et al. Among authors: figuera le. Arch Soc Esp Oftalmol. 2012 Nov;87(11):373-5. doi: 10.1016/j.oftal.2011.09.008. Epub 2012 May 24. Arch Soc Esp Oftalmol. 2012. PMID: 23058197 Spanish.

5

Pedigree analysis of Mexican families with Fabry disease as a powerful tool for identification of heterozygous females.

Gutiérrez-Amavizca BE, Orozco-Castellanos R, R Padilla-Gutiérrez J, Valle Y, Figuera LE. Gutiérrez-Amavizca BE, et al. Among authors: figuera le. Genet Mol Res. 2014 Aug 28;13(3):6752-8. doi: 10.4238/2014.August.28.19. Genet Mol Res. 2014. PMID: 25177955 Free article.

6

Prediction of Regulatory SNPs in Putative Minor Genes of the Neuro-Cardiovascular Variant in Fabry Reveals Insights into Autophagy/Apoptosis and Fibrosis.

Ruiz Ramírez AV, Prado Montes de Oca E, Figuera LE. Ruiz Ramírez AV, et al. Among authors: figuera le. Biology (Basel). 2022 Aug 30;11(9):1287. doi: 10.3390/biology11091287. Biology (Basel). 2022. PMID: 36138766 Free PMC article.

7

[Current genetic issues and phenotypic variants in Kallmann syndrome].

Gutiérrez-Amavizca BE, Figuera LE, Orozco-Castellanos R. Gutiérrez-Amavizca BE, et al. Among authors: figuera le. Rev Med Inst Mex Seguro Soc. 2012 Mar-Apr;50(2):157-61. Rev Med Inst Mex Seguro Soc. 2012. PMID: 22882983 Review. Spanish.

8

Association of the FTO gene SNP rs17817449 with body fat distribution in Mexican women.

Zermeño-Rivera JJ, Astocondor-Pérez JP, Valle Y, Padilla-Gutiérrez JR, Orozco-Castellanos R, Figuera LE, Gutiérrez-Amavizca BE. Zermeño-Rivera JJ, et al. Among authors: figuera le. Genet Mol Res. 2014 Feb 13;13(4):8561-7. doi: 10.4238/2014.February.13.7. Genet Mol Res. 2014. PMID: 24615093 Free article.

9

SNP 668C (-44) alters a NF-kappaB1 putative binding site in non-coding strand of human beta-defensin 1 (DEFB1) and is associated with lepromatous leprosy.

Prado-Montes de Oca E, Velarde-Félix JS, Ríos-Tostado JJ, Picos-Cárdenas VJ, Figuera LE. Prado-Montes de Oca E, et al. Among authors: figuera le. Infect Genet Evol. 2009 Jul;9(4):617-25. doi: 10.1016/j.meegid.2009.03.006. Epub 2009 Apr 5. Infect Genet Evol. 2009. PMID: 19460328

10

eNOS gene Glu298Asp and 4b/a polymorphisms are associated with renal function parameters in Mexican patients with Fabry disease.

Marin-Medina A, Brambila-Tapia AJ, Picos-Cárdenas VJ, Gallegos-Arreola MP, Figuera LE. Marin-Medina A, et al. Among authors: figuera le. Genet Mol Res. 2016 Oct 24;15(4). doi: 10.4238/gmr15047802. Genet Mol Res. 2016. PMID: 27813552 Free article.

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