Chacon-Camacho OF - Search Results

1

Genetic Aspects of Glaucoma: An Updated Review.

Chacon-Camacho OF, Arce-Gonzalez R, Sanchez-de la Rosa F, Urióstegui-Rojas A, Hofmann-Blancas ME, Mata-Flores F, Zenteno JC. Chacon-Camacho OF, et al. Curr Mol Med. 2024;24(10):1231-1249. doi: 10.2174/1566524023666230602143617. Curr Mol Med. 2024. PMID: 37272463 Review.

2

Clinical and molecular features of familial and sporadic cases of von Hippel-Lindau disease from Mexico.

Chacon-Camacho OF, Rodriguez-Dennen F, Camacho-Molina A, Rasmussen A, Alonso-Vilatela E, Zenteno JC. Chacon-Camacho OF, et al. Clin Exp Ophthalmol. 2010 Apr;38(3):277-83. doi: 10.1111/j.1442-9071.2010.02241.x. Clin Exp Ophthalmol. 2010. PMID: 20447124

3

OCT findings in young asymptomatic subjects carrying familial BEST1 gene mutations.

Chacon-Camacho OF, Camarillo-Blancarte L, Zenteno JC. Chacon-Camacho OF, et al. Ophthalmic Genet. 2011 Mar;32(1):24-30. doi: 10.3109/13816810.2010.524906. Epub 2010 Nov 15. Ophthalmic Genet. 2011. PMID: 21077756

4

Expanding the phenotype of gingival fibromatosis-mental retardation-hypertrichosis (Zimmermann-Laband) syndrome.

Chacon-Camacho OF, Vázquez J, Zenteno JC. Chacon-Camacho OF, et al. Am J Med Genet A. 2011 Jul;155A(7):1716-20. doi: 10.1002/ajmg.a.34030. Epub 2011 May 27. Am J Med Genet A. 2011. PMID: 21626675

5

Klippel-Feil syndrome associated with situs inversus: description of a new case and exclusion of GDF1, GDF3 and GDF6 as causal genes.

Chacón-Camacho O, Camarillo-Blancarte L, Pelaez-González H, Mendiola J, Zenteno JC. Chacón-Camacho O, et al. Eur J Med Genet. 2012 Jun;55(6-7):414-7. doi: 10.1016/j.ejmg.2012.03.007. Epub 2012 Mar 28. Eur J Med Genet. 2012. PMID: 22522086

6

Expansion of the clinical ocular spectrum of Wolfram Syndrome in a family carrying a novel WFS1 gene deletion.

Chacón-Camacho O, Arce-Gonzalez R, Granillo-Alvarez M, Flores-Limas S, Ramírez M, Zenteno JC. Chacón-Camacho O, et al. Ophthalmic Genet. 2013 Dec;34(4):243-8. doi: 10.3109/13816810.2012.755631. Epub 2013 Feb 1. Ophthalmic Genet. 2013. PMID: 23373429

7

ABCA4 mutational spectrum in Mexican patients with Stargardt disease: Identification of 12 novel mutations and evidence of a founder effect for the common p.A1773V mutation.

Chacón-Camacho OF, Granillo-Alvarez M, Ayala-Ramírez R, Zenteno JC. Chacón-Camacho OF, et al. Exp Eye Res. 2013 Apr;109:77-82. doi: 10.1016/j.exer.2013.02.006. Epub 2013 Feb 16. Exp Eye Res. 2013. PMID: 23419329

8

A Novel De Novo EFNB1 Gene Mutation in a Mexican Patient with Craniofrontonasal Syndrome.

Ramirez-Garcia MA, Chacon-Camacho OF, Leyva-Hernandez C, Cardenas-Conejo A, Zenteno JC. Ramirez-Garcia MA, et al. Case Rep Genet. 2013;2013:349725. doi: 10.1155/2013/349725. Epub 2013 Feb 21. Case Rep Genet. 2013. PMID: 23509643 Free PMC article.

9

Nasopalpebral lipoma-coloboma syndrome: clinical, radiological, and histopathological description of a novel sporadic case.

Chacon-Camacho OF, Lopez-Martinez MS, Vázquez J, Nava-Castañeda A, Martin-Biasotti F, Piña-Aguilar RE, Iñiguez-Soto M, Acosta-García J, Zenteno JC. Chacon-Camacho OF, et al. Am J Med Genet A. 2013 Jun;161A(6):1470-4. doi: 10.1002/ajmg.a.35916. Epub 2013 May 1. Am J Med Genet A. 2013. PMID: 23636874

10

[Prenatal exclusion of von Hippel-Lindau syndrome in a Mexican family carrying a novel VHL gene mutation].

Chacón-Camacho OF, Benitez-Granados J, Zenteno JC. Chacón-Camacho OF, et al. Ginecol Obstet Mex. 2013 Apr;81(4):206-10. Ginecol Obstet Mex. 2013. PMID: 23720934 Spanish.

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