Gutiérrez-Amavizca BE - Search Results

1

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

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

2

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. J Genet. 2017 Mar;96(1):161-164. doi: 10.1007/s12041-017-0744-4. J Genet. 2017. PMID: 28360401 Free article.

3

Neuhauser syndrome: a rare association of megalocornea and mental retardation. Review of the literature and further phenotype delineation.

Gutiérrez-Amavizca BE, Juárez-Vázquez CI, Orozco-Castellanos R, Arnaud L, Macías-Gómez NM, Barros-Nuñez P. Gutiérrez-Amavizca BE, et al. Genet Couns. 2013;24(2):185-91. Genet Couns. 2013. PMID: 24032289 Review.

4

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. 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.

5

Faciocardiorenal syndrome: a wide clinical spectrum?

Brambila Tapia AJ, Vásquez Velásque AI, González Mercado MG, Macías Chumacera A, Gutierrez-Amavizca BE, Lara Aguilar RA, Pérez Juárez CR, Moreno Andrade A, Figuera LE. Brambila Tapia AJ, et al. Genet Couns. 2012;23(1):51-6. Genet Couns. 2012. PMID: 22611642

6

[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. 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.

7

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: gutierrez amavizca be. 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.

8

Contribution of GSTM1, GSTT1, and MTHFR polymorphisms to end-stage renal disease of unknown etiology in Mexicans.

Gutiérrez-Amavizca BE, Orozco-Castellanos R, Ortíz-Orozco R, Padilla-Gutiérrez J, Valle Y, Gutiérrez-Gutiérrez N, García-García G, Gallegos-Arreola M, Figuera LE. Gutiérrez-Amavizca BE, et al. Indian J Nephrol. 2013 Nov;23(6):438-43. doi: 10.4103/0971-4065.120342. Indian J Nephrol. 2013. PMID: 24339523 Free PMC article.

9

Two familial intrachromosomal insertions with maternal dup(6)(p22.3p25.3) or dup(2)(q24.2q32.1) in recombinant offspring.

Domínguez MG, Rivera H, Aguilar-Lemarroy A, Jave-Suarez LF, Ramírez-Velazco A, González-Ramos IA, Barros-Núñez P, Partida-Pérez M, Gutiérrez-Amavizca BE, Brambila-Tapia AJ, Figuera LE. Domínguez MG, et al. Among authors: gutierrez amavizca be. Clin Dysmorphol. 2017 Oct;26(4):209-216. doi: 10.1097/MCD.0000000000000191. Clin Dysmorphol. 2017. PMID: 28737552

10

[Genetic contribution in primary sleep disorders].

Gutiérrez-Amavizca BE, Gutiérrez-Amavizca JP, Pérez-León JA. Gutiérrez-Amavizca BE, et al. Rev Med Inst Mex Seguro Soc. 2019 Apr 1;57(1):21-29. Rev Med Inst Mex Seguro Soc. 2019. PMID: 31071251 Review. Spanish.

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