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Presymptomatic Testing for Huntington's Disease in Mexico: 28 Years of Experience.
Ochoa-Morales A, Dávila-Ortiz de Montellano DJ, Chávez-Oliveros M, Rodríguez-Agudelo Y, Longoria-Ibarrola M, Sosa-Ortiz AL, Boll MC, Jara-Prado A, Yescas-Gómez P, Guerrero-Camacho J, Ramírez-García MÁ. Ochoa-Morales A, et al. Among authors: yescas gomez p. Arch Med Res. 2024 May 6;55(4):103004. doi: 10.1016/j.arcmed.2024.103004. Online ahead of print. Arch Med Res. 2024. PMID: 38714041
[Frequency of apolipoprotein E in a Nahua population].
Suástegui Román RA, Yescas Gómez P, Guerrero Camacho JL, Ochoa Morales A, Granados J, Jara Prado A, López-Caro OA, Alonso Vilatela ME. Suástegui Román RA, et al. Rev Invest Clin. 2002 Sep-Oct;54(5):415-21. Rev Invest Clin. 2002. PMID: 12587416 Spanish.
The ATP-binding cassette transporter A1 R230C variant affects HDL cholesterol levels and BMI in the Mexican population: association with obesity and obesity-related comorbidities.
Villarreal-Molina MT, Aguilar-Salinas CA, Rodríguez-Cruz M, Riaño D, Villalobos-Comparan M, Coral-Vazquez R, Menjivar M, Yescas-Gomez P, Königsoerg-Fainstein M, Romero-Hidalgo S, Tusie-Luna MT, Canizales-Quinteros S; Metabolic Study Group. Villarreal-Molina MT, et al. Diabetes. 2007 Jul;56(7):1881-7. doi: 10.2337/db06-0905. Epub 2007 Feb 7. Diabetes. 2007. PMID: 17287470
Association of R230C ABCA1 gene variant with low HDL-C levels and abnormal HDL subclass distribution in Mexican school-aged children.
Flores-Dorantes T, Arellano-Campos O, Posadas-Sánchez R, Villarreal-Molina T, Medina-Urrutia A, Romero-Hidalgo S, Yescas-Gómez P, Pérez-Méndez O, Jorge-Galarza E, Tusié-Luna T, Villalobos-Comparán M, Jacobo-Albavera L, Villamil-Ramírez H, López-Contreras BE, Aguilar-Salinas CA, Posadas-Romero C, Canizales-Quinteros S. Flores-Dorantes T, et al. Clin Chim Acta. 2010 Sep 6;411(17-18):1214-7. doi: 10.1016/j.cca.2010.04.025. Epub 2010 Apr 26. Clin Chim Acta. 2010. PMID: 20427018
Genetics of Alzheimer's disease.
Alonso Vilatela ME, López-López M, Yescas-Gómez P. Alonso Vilatela ME, et al. Arch Med Res. 2012 Nov;43(8):622-31. doi: 10.1016/j.arcmed.2012.10.017. Epub 2012 Nov 8. Arch Med Res. 2012. PMID: 23142261 Free article. Review.
DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseases.
Bettencourt C, Hensman-Moss D, Flower M, Wiethoff S, Brice A, Goizet C, Stevanin G, Koutsis G, Karadima G, Panas M, Yescas-Gómez P, García-Velázquez LE, Alonso-Vilatela ME, Lima M, Raposo M, Traynor B, Sweeney M, Wood N, Giunti P; SPATAX Network; Durr A, Holmans P, Houlden H, Tabrizi SJ, Jones L. Bettencourt C, et al. Among authors: yescas gomez p. Ann Neurol. 2016 Jun;79(6):983-90. doi: 10.1002/ana.24656. Epub 2016 May 6. Ann Neurol. 2016. PMID: 27044000 Free PMC article.
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