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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2008 1
2009 3
2010 2
2011 1
2015 1
2016 3
2018 4
2019 3
2020 4
2021 3
2022 2
2024 0

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24 results

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Page 1
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.
The relevance of the cytogenetic analysis in syndromic microphthalmia/anophthalmia.
Apam-Garduño D, Cortés-González V, Quintana-Fernández L, Martínez-Anaya D, Pérez-Vera P, Villanueva-Mendoza C. Apam-Garduño D, et al. Among authors: villanueva mendoza c. Ophthalmic Genet. 2019 Dec;40(6):584-587. doi: 10.1080/13816810.2019.1698618. Epub 2019 Dec 6. Ophthalmic Genet. 2019. PMID: 31809626 No abstract available.
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. Among authors: villanueva mendoza c. Int Ophthalmol. 2016 Feb;36(1):111-120. doi: 10.1007/s10792-015-0085-3. Epub 2015 May 26. Int Ophthalmol. 2016. PMID: 26003990
An unusual ocular birth injury.
Ceriotto-García A, Pérez-Alarcón B, Villanueva-Mendoza C, Salcedo-Casillas G. Ceriotto-García A, et al. Among authors: villanueva mendoza c. Can J Ophthalmol. 2009 Apr;44(2):215-6. doi: 10.3129/i09-008. Can J Ophthalmol. 2009. PMID: 19491965 No abstract available.
Vitreous involvement as initial presentation of hereditary transthyretin amyloidosis related to the rare TTR Ile107Met (p.Ile127Met) pathogenic variant.
Treviño-Herrera AB, Bustamante-Vargas AP, Lisker-Cervantes A, Ríos Y Valles Valles D, Villanueva-Mendoza C, González-Duarte A, Concha-Del-Río LE. Treviño-Herrera AB, et al. Among authors: villanueva mendoza c. Ophthalmic Genet. 2022 Jun;43(3):413-419. doi: 10.1080/13816810.2022.2025606. Epub 2022 Jan 17. Ophthalmic Genet. 2022. PMID: 35038954
Mosaic cat eye syndrome in a child with unilateral iris coloboma.
Hernández-Medrano C, Hidalgo-Bravo A, Villanueva-Mendoza C, Bautista-Tirado T, Apam-Garduño D. Hernández-Medrano C, et al. Among authors: villanueva mendoza c. Ophthalmic Genet. 2021 Feb;42(1):84-87. doi: 10.1080/13816810.2020.1839918. Epub 2020 Dec 1. Ophthalmic Genet. 2021. PMID: 33465332
Increasing the Genetic Diagnosis Yield in Inherited Retinal Dystrophies: Assigning Pathogenicity to Novel Non-canonical Splice Site Variants.
Toulis V, Cortés-González V, Castro-Miró M, Sallum JF, Català-Mora J, Villanueva-Mendoza C, Ciccioli M, Gonzàlez-Duarte R, Valero R, Marfany G. Toulis V, et al. Among authors: villanueva mendoza c. Genes (Basel). 2020 Mar 31;11(4):378. doi: 10.3390/genes11040378. Genes (Basel). 2020. PMID: 32244552 Free PMC article.
24 results