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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. Among authors: figuera le. Genet Couns. 2012;23(1):51-6. Genet Couns. 2012. PMID: 22611642
[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.
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. Among authors: figuera le. Indian J Nephrol. 2013 Nov;23(6):438-43. doi: 10.4103/0971-4065.120342. Indian J Nephrol. 2013. PMID: 24339523 Free PMC article.
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.
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: figuera le. Clin Dysmorphol. 2017 Oct;26(4):209-216. doi: 10.1097/MCD.0000000000000191. Clin Dysmorphol. 2017. PMID: 28737552
111 results