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Extensive genic and allelic heterogeneity underlying inherited retinal dystrophies in Mexican patients molecularly analyzed by next-generation sequencing.
Zenteno JC, García-Montaño LA, Cruz-Aguilar M, Ronquillo J, Rodas-Serrano A, Aguilar-Castul L, Matsui R, Vencedor-Meraz CI, Arce-González R, Graue-Wiechers F, Gutiérrez-Paz M, Urrea-Victoria T, de Dios Cuadras U, Chacón-Camacho OF. Zenteno JC, et al. Among authors: de dios cuadras u. Mol Genet Genomic Med. 2020 Jan;8(1):10.1002/mgg3.1044. doi: 10.1002/mgg3.1044. Epub 2019 Nov 17. Mol Genet Genomic Med. 2020. PMID: 31736247 Free PMC article.
Roth spots as debut of multiple myeloma.
Díazceballos-García AL, de Dios-Cuadras U, Graue-Wiechers F. Díazceballos-García AL, et al. Among authors: de dios cuadras u. Can J Ophthalmol. 2021 Apr;56(2):144-145. doi: 10.1016/j.jcjo.2020.08.007. Epub 2020 Sep 17. Can J Ophthalmol. 2021. PMID: 32950469 No abstract available.
X-linked juvenile retinoschisis associated with an RS1 in-frame deletion and bilateral central serous chorioretinopathy.
Wheelock-Gutierrez L, Peña-Ortiz S, de Dios-Cuadras U, Jiménez-Sierra JM, Zenteno JC, Payro-Evia K, Dorantes-Diez MA, Enriquez-Gonzalez AB. Wheelock-Gutierrez L, et al. Among authors: de dios cuadras u. Retin Cases Brief Rep. 2023 Aug 8. doi: 10.1097/ICB.0000000000001472. Online ahead of print. Retin Cases Brief Rep. 2023. PMID: 37582336
Primary Cancer Sites and Clinical Features of Choroidal Metastasis in Mexican Patients.
Salcedo-Villanueva G, Medina-Andrade AA, Moreno-Paramo D, Golzarri MF, Moreno-Paramo E, Ortiz-Ramirez GY, Martinez-Aguilar U, De Dios-Cuadras U, Jimenez-Rodriguez M, Espinosa-Soto I, Mira-Lorenzo X, Guzman-Cerda J, Orozco-Moguel A, Becerra-Revollo C, Orozco-Gomez LP, Fulda E. Salcedo-Villanueva G, et al. Among authors: de dios cuadras u. Clin Ophthalmol. 2021 Jan 19;15:201-209. doi: 10.2147/OPTH.S285250. eCollection 2021. Clin Ophthalmol. 2021. PMID: 33500613 Free PMC article.