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Out-of-pocket expenditures and care time for children with Down Syndrome: A single-hospital study in Mexico City.
Martínez-Valverde S, Salinas-Escudero G, García-Delgado C, Garduño-Espinosa J, Morán-Barroso VF, Granados-García V, Tiro-Sánchez MT, Toledano-Toledano F, Aldaz-Rodríguez MV. Martínez-Valverde S, et al. PLoS One. 2019 Jan 10;14(1):e0208076. doi: 10.1371/journal.pone.0208076. eCollection 2019. PLoS One. 2019. PMID: 30629602 Free PMC article.
Cytogenetic profile in 1,921 cases of trisomy 21 syndrome.
Flores-Ramírez F, Palacios-Guerrero C, García-Delgado C, Morales-Jiménez AB, Arias-Villegas CM, Cervantes A, Morán-Barroso VF. Flores-Ramírez F, et al. Arch Med Res. 2015 Aug;46(6):484-9. doi: 10.1016/j.arcmed.2015.08.001. Epub 2015 Aug 24. Arch Med Res. 2015. PMID: 26314225
Congenital hypertrichosis universalis in Mexican female twins.
Cervantes A, García-Delgado C, Fernández-Ramírez F, Valencia-Herrera A, Kofman S, Morán-Barroso V. Cervantes A, et al. Int J Dermatol. 2016 Jan;55(1):e29-31. doi: 10.1111/ijd.13104. Epub 2015 Oct 30. Int J Dermatol. 2016. PMID: 26518157 Review. No abstract available.
[Pallister-Killian syndrome in a Mexican mestizo patient. Case report].
Mendelsberg-Fishbein P, García-Delgado C, Muñoz-Martínez LB, Robledo-Cayetano M, Mejía-Marín LJ, Martínez-Barrera LE, Cerrillo-Hinojosa M, Moran-Barroso VF. Mendelsberg-Fishbein P, et al. Arch Argent Pediatr. 2018 Feb 1;116(1):e135-e138. doi: 10.5546/aap.2018.e135. Arch Argent Pediatr. 2018. PMID: 29333839 Free article. Spanish.
Silver-Russell syndrome caused by trisomy 11p15.5 due to a derivative X chromosome from a de novo t(X;11) in a Mexican female patient.
Paz-Ramírez M, Muñoz-Martínez LB, Morales-Jiménez AB, Morán-Barroso VF, García-Delgado C, Azotla-Vilchis CN, Márquez-Quiroz LC, Astiazarán MC. Paz-Ramírez M, et al. Among authors: garcia delgado c. Clin Dysmorphol. 2022 Apr 1;31(2):94-97. doi: 10.1097/MCD.0000000000000402. Clin Dysmorphol. 2022. PMID: 34750319 No abstract available.
X-linked hypohidrotic ectodermal dysplasia by a de novo recurrent variant in a Mexican patient.
Noriega-Juárez MA, García-Delgado C, Villaseñor-Domínguez A, Mena-Cedillos CA, Toledo-Bahena M, Valencia-Herrera A, Baeza-Capetillo P, Cervantes A, Morán-Barroso VF, Monroy-Jaramillo N. Noriega-Juárez MA, et al. Bol Med Hosp Infant Mex. 2020;77(4):212-217. doi: 10.24875/BMHIM.19000209. Bol Med Hosp Infant Mex. 2020. PMID: 32713954 English.
61 results