Villanueva-Mendoza C - Search Results

1

Progression of gyrate atrophy measured with ultra-wide-field imaging.

Salcedo-Villanueva G, Paciuc-Beja M, Villanueva-Mendoza C, Harasawa M, Smith JM, Velez-Montoya R, Olson JL, Oliver SC, Mandava N, Quiroz-Mercado H. Salcedo-Villanueva G, et al. Int Ophthalmol. 2016 Feb;36(1):111-120. doi: 10.1007/s10792-015-0085-3. Epub 2015 May 26. Int Ophthalmol. 2016. PMID: 26003990

2

Macular optical coherence tomography findings and GPR143 mutations in patients with ocular albinism.

Sepúlveda-Vázquez HE, Villanueva-Mendoza C, Zenteno JC, Villegas-Ruiz V, Pelcastre-Luna E, García-Aguirre G. Sepúlveda-Vázquez HE, et al. Int Ophthalmol. 2014 Oct;34(5):1075-81. doi: 10.1007/s10792-014-9912-1. Epub 2014 Feb 14. Int Ophthalmol. 2014. PMID: 24526317

3

Autofluorescence in female carriers with choroideremia: A familial case with a novel mutation in the CHM gene.

Ortiz-Ramirez GY, Villanueva-Mendoza C, Zenteno Ruiz JC, Reyes M, Cortés-González V. Ortiz-Ramirez GY, et al. Among authors: villanueva mendoza c. Ophthalmic Genet. 2020 Dec;41(6):625-628. doi: 10.1080/13816810.2020.1810283. Epub 2020 Aug 24. Ophthalmic Genet. 2020. PMID: 32835561

4

[Extension of TORCH spectrum in ophthalmology: congenital Zika, case report].

Pando-Cifuentes A, Cortés-González V, Berrones-Medina D, Villanueva-Mendoza C. Pando-Cifuentes A, et al. Among authors: villanueva mendoza c. Rev Med Inst Mex Seguro Soc. 2019 Dec 30;57(6):395-399. Rev Med Inst Mex Seguro Soc. 2019. PMID: 33001616 Spanish.

5

Unraveling the genetic complexities of combined retinal dystrophy and hearing impairment.

Bahena P, Daftarian N, Maroofian R, Linares P, Villalobos D, Mirrahimi M, Rad A, Doll J, Hofrichter MAH, Koparir A, Röder T, Han S, Sabbaghi H, Ahmadieh H, Behboudi H, Villanueva-Mendoza C, Cortés-Gonzalez V, Zamora-Ortiz R, Kohl S, Kuehlewein L, Darvish H, Alehabib E, Arenas-Sordo ML, Suri F, Vona B, Haaf T. Bahena P, et al. Among authors: villanueva mendoza c. Hum Genet. 2022 Apr;141(3-4):785-803. doi: 10.1007/s00439-021-02303-1. Epub 2021 Jun 20. Hum Genet. 2022. PMID: 34148116 Free PMC article.

6

The Genetic Landscape of Inherited Retinal Diseases in a Mexican Cohort: Genes, Mutations and Phenotypes.

Villanueva-Mendoza C, Tuson M, Apam-Garduño D, de Castro-Miró M, Tonda R, Trotta JR, Marfany G, Valero R, Cortés-González V, Gonzàlez-Duarte R. Villanueva-Mendoza C, et al. Genes (Basel). 2021 Nov 19;12(11):1824. doi: 10.3390/genes12111824. Genes (Basel). 2021. PMID: 34828430 Free PMC article.

7

Novel and recurrent NDP gene mutations in familial cases of Norrie disease and X-linked exudative vitreoretinopathy.

Pelcastre EL, Villanueva-Mendoza C, Zenteno JC. Pelcastre EL, et al. Clin Exp Ophthalmol. 2010 May;38(4):367-74. doi: 10.1111/j.1442-9071.2010.02245.x. Epub 2010 Feb 22. Clin Exp Ophthalmol. 2010. PMID: 20491809

8

Triple A or Allgrove syndrome. A case report with ophthalmic abnormalities and a novel mutation in the AAAS gene.

Villanueva-Mendoza C, artínez-Guzmán O, Rivera-Parra D, Zenteno JC. Villanueva-Mendoza C, et al. Ophthalmic Genet. 2009 Mar;30(1):45-9. doi: 10.1080/13816810802502962. Ophthalmic Genet. 2009. PMID: 19172511

9

Mutational screening of CHX10, GDF6, OTX2, RAX and SOX2 genes in 50 unrelated microphthalmia-anophthalmia-coloboma (MAC) spectrum cases.

Gonzalez-Rodriguez J, Pelcastre EL, Tovilla-Canales JL, Garcia-Ortiz JE, Amato-Almanza M, Villanueva-Mendoza C, Espinosa-Mattar Z, Zenteno JC. Gonzalez-Rodriguez J, et al. Br J Ophthalmol. 2010 Aug;94(8):1100-4. doi: 10.1136/bjo.2009.173500. Epub 2010 May 21. Br J Ophthalmol. 2010. PMID: 20494911

10

Familial case of Blau syndrome associated with a CARD15/NOD2 mutation.

Villanueva-Mendoza C, Arellanes-García L, Cubas-Lorenzo V, Jimenez-Martinez MC, Flores-Suárez LF, Zenteno JC. Villanueva-Mendoza C, et al. Ophthalmic Genet. 2010 Sep;31(3):155-8. doi: 10.3109/13816810.2010.492818. Ophthalmic Genet. 2010. PMID: 20565245

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