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Year Number of Results
2002 1
2003 1
2008 2
2011 2
2013 1
2014 2
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2018 1
2019 2
2021 1
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2024 2

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Page 1
Clinical and Genetic Characterization of RDH12-Retinal Dystrophy in a South American Cohort.
Daich Varela M, Moya R, Azevedo Souza Amaral R, Schlottmann PG, Álvarez Mendiara A, Francone A, Guazi Resende R, Capalbo L, Gelvez N, López G, Morales-Acevedo AM, Ossa RH, Arno G, Michaelides M, Tamayo ML, Ferraz Sallum JM. Daich Varela M, et al. Among authors: gelvez n. Ophthalmol Retina. 2024 Feb;8(2):163-173. doi: 10.1016/j.oret.2023.09.007. Epub 2023 Sep 13. Ophthalmol Retina. 2024. PMID: 37714431 Free article.
Detection of hearing loss in newborns: Definition of a screening strategy in Bogotá, Colombia.
Olarte M, Bermúdez Rey MC, Beltran AP, Guerrero D, Suárez-Obando F, López G, García M, Ospina JC, Fonseca C, Bertolotto AM, Aldana N, Gelvez N, Tamayo ML. Olarte M, et al. Among authors: gelvez n. Int J Pediatr Otorhinolaryngol. 2019 Jul;122:76-81. doi: 10.1016/j.ijporl.2019.03.016. Epub 2019 Mar 26. Int J Pediatr Otorhinolaryngol. 2019. PMID: 30978473
Novel Cases of Non-Syndromic Hearing Impairment Caused by Pathogenic Variants in Genes Encoding Mitochondrial Aminoacyl-tRNA Synthetases.
Domínguez-Ruiz M, Olarte M, Onecha E, García-Vaquero I, Gelvez N, López G, Villamar M, Morín M, Moreno-Pelayo MA, Morales-Angulo C, Polo R, Tamayo ML, Del Castillo I. Domínguez-Ruiz M, et al. Among authors: gelvez n. Genes (Basel). 2024 Jul 19;15(7):951. doi: 10.3390/genes15070951. Genes (Basel). 2024. PMID: 39062730 Free PMC article.
18 results