Yerlin Chacón-Camacho - Search Results

Year	Number of Results
2010	3
2011	2
2012	2
2013	9
2014	7
2015	5
2016	5
2017	6
2018	5
2019	5
2020	6
2021	1
2022	7
2023	7
2024	1

1

Familial Hypercholesterolemia: Update and Review.

Chacón-Camacho OF, Pozo-Molina G, Méndez-Catalá CF, Reyes-Reali J, Méndez-Cruz R, Zenteno JC. Chacón-Camacho OF, et al. Endocr Metab Immune Disord Drug Targets. 2022;22(2):198-211. doi: 10.2174/1871530321666210208212148. Endocr Metab Immune Disord Drug Targets. 2022. PMID: 33563162

2

Genetic Aspects of Glaucoma: An Updated Review.

Chacon-Camacho OF, Arce-Gonzalez R, Sanchez-de la Rosa F, Urióstegui-Rojas A, Hofmann-Blancas EM, Mata-Flores F, Zenteno JC. Chacon-Camacho OF, et al. Curr Mol Med. 2023 Jun 2. doi: 10.2174/1566524023666230602143617. Online ahead of print. Curr Mol Med. 2023. PMID: 37272463

3

The clinical implications of molecular monitoring and analyses of inherited retinal diseases.

Chacón-Camacho OF, García-Montaño LA, Zenteno JC. Chacón-Camacho OF, et al. Expert Rev Mol Diagn. 2017 Nov;17(11):1009-1021. doi: 10.1080/14737159.2017.1384314. Epub 2017 Oct 5. Expert Rev Mol Diagn. 2017. PMID: 28945154 Review.

4

Newborn transient patterned hyperpigmentation and anophthalmia.

Chacón Camacho OF, Arce-González R, Rodríguez Uribe G. Chacón Camacho OF, et al. Bol Med Hosp Infant Mex. 2020;77(3):146-148. doi: 10.24875/BMHIM.19000191. Bol Med Hosp Infant Mex. 2020. PMID: 32496470 English.

5

Review and update on the molecular basis of Leber congenital amaurosis.

Chacon-Camacho OF, Zenteno JC. Chacon-Camacho OF, et al. World J Clin Cases. 2015 Feb 16;3(2):112-24. doi: 10.12998/wjcc.v3.i2.112. World J Clin Cases. 2015. PMID: 25685757 Free PMC article. Review.

6

[Gene therapy for hereditary ophthalmological diseases: Advances and future perspectives].

Chacón-Camacho ÓF, Astorga-Carballo A, Zenteno JC. Chacón-Camacho ÓF, et al. Gac Med Mex. 2015 Jul-Aug;151(4):501-11. Gac Med Mex. 2015. PMID: 26290027 Free article. Review. Spanish.

7

Sclerocornea-Microphthalmia-Aphakia Complex: Description of Two Additional Cases Associated With Novel FOXE3 Mutations and Review of the Literature.

Quiroz-Casian N, Chacon-Camacho OF, Barragan-Arevalo T, Nava-Valdez J, Lieberman E, Salgado-Medina A, Navas A, Graue-Hernandez EO, Zenteno JC. Quiroz-Casian N, et al. Cornea. 2018 Sep;37(9):1178-1181. doi: 10.1097/ICO.0000000000001655. Cornea. 2018. PMID: 29878917 Review.

8

Novel FREM1 mutations in a patient with MOTA syndrome: Clinical findings, mutation update and review of FREM1-related disorders literature.

Chacon-Camacho OF, Zenker M, Schanze D, Ledesma-Gil J, Zenteno JC. Chacon-Camacho OF, et al. Eur J Med Genet. 2017 Mar;60(3):190-194. doi: 10.1016/j.ejmg.2017.01.005. Epub 2017 Jan 19. Eur J Med Genet. 2017. PMID: 28111185 Review.

9

Learning from history in the midst of the COVID-19: epidemics/pandemics of antiquity up to the fall of the Western Roman Empire.

Chacón-Camacho ÓF, Arce-González R, Zenteno JC, Granillo MT. Chacón-Camacho ÓF, et al. Bol Med Hosp Infant Mex. 2023;80(5):269-278. doi: 10.24875/BMHIM.22000147. Bol Med Hosp Infant Mex. 2023. PMID: 37963299 Free article. English.

10

SOX2 anophthalmia syndrome and dental anomalies.

Chacon-Camacho OF, Fuerte-Flores BI, Ricardez-Marcial EF, Zenteno JC. Chacon-Camacho OF, et al. Am J Med Genet A. 2015 Nov;167A(11):2830-3. doi: 10.1002/ajmg.a.37277. Epub 2015 Aug 6. Am J Med Genet A. 2015. PMID: 26250054

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