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Page 1
Low bone mineral density and renal malformation in Mexican patients with Turner syndrome are associated with single nucleotide variants in vitamin D-metabolism genes.
Barrientos-Rios R, Frias S, Velázquez-Aragón JA, Villaroel CE, Sánchez S, Molina B, Martínez A, Carnevale A, García-de-Teresa B, Bonilla E, Alvarado-Araiza CD, Valderrama-Hernández A, Ríos-Gallardo PT, Calzada-León R, Altamirano-Bustamante N, Torres L. Barrientos-Rios R, et al. Gynecol Endocrinol. 2019 Sep;35(9):772-776. doi: 10.1080/09513590.2019.1582626. Epub 2019 Mar 19. Gynecol Endocrinol. 2019. PMID: 30887870 Free article.
Analysis of the glucokinase gene in Mexican families displaying early-onset non-insulin-dependent diabetes mellitus including MODY families.
del Bosque-Plata L, García-García E, Ramírez-Jiménez S, Cabello-Villegas J, Riba L, Gómez-León A, Vega-Hernández G, Altamirano-Bustamante N, Calzada-León R, Robles-Valdés C, Mendoza-Morfín F, Curiel-Pérez O, Tusié-Luna MT. del Bosque-Plata L, et al. Am J Med Genet. 1997 Nov 12;72(4):387-93. doi: 10.1002/(sici)1096-8628(19971112)72:4<387::aid-ajmg3>3.0.co;2-o. Am J Med Genet. 1997. PMID: 9375718
Molecular genetic analysis of patients carrying steroid 21-hydroxylase deficiency in the Mexican population: identification of possible new mutations and high prevalence of apparent germ-line mutations.
Ordoñez-Sánchez ML, Ramírez-Jiménez S, López-Gutierrez AU, Riba L, Gamboa-Cardiel S, Cerrillo-Hinojosa M, Altamirano-Bustamante N, Calzada-León R, Robles-Valdés C, Mendoza-Morfin F, Tusié-Luna MT. Ordoñez-Sánchez ML, et al. Hum Genet. 1998 Feb;102(2):170-7. doi: 10.1007/s004390050672. Hum Genet. 1998. PMID: 9580109
Unpacking the aggregation-oligomerization-fibrillization process of naturally-occurring hIAPP amyloid oligomers isolated directly from sera of children with obesity or diabetes mellitus.
Altamirano-Bustamante MM, Altamirano-Bustamante NF, Larralde-Laborde M, Lara-Martínez R, Leyva-García E, Garrido-Magaña E, Rojas G, Jiménez-García LF, Revilla-Monsalve C, Altamirano P, Calzada-León R. Altamirano-Bustamante MM, et al. Sci Rep. 2019 Dec 5;9(1):18465. doi: 10.1038/s41598-019-54570-8. Sci Rep. 2019. PMID: 31804529 Free PMC article.
Growth charts for Mexican children with Down syndrome.
Flores Arizmendi KA, García De La Puente S, González Navarro M, Bonillo Suarez L, De León Becerra AG, Valderrama Hernández A, Santos Ríos R, Altamirano Bustamante N. Flores Arizmendi KA, et al. Among authors: altamirano bustamante n. Am J Med Genet A. 2022 Apr;188(4):1170-1183. doi: 10.1002/ajmg.a.62637. Epub 2022 Jan 9. Am J Med Genet A. 2022. PMID: 35001493
Mutations in MODY genes are not common cause of early-onset type 2 diabetes in Mexican families.
Domínguez-López A, Miliar-García A, Segura-Kato YX, Riba L, Esparza-López R, Ramírez-Jiménez S, Rodríguez-Torres M, Canizales-Quinteros S, Cabrera-Vásquez S, Fragoso-Ontiveros V, Aguilar-Salinas CA, Altamirano-Bustamante N, Calzada-León R, Robles-Valdés C, Bravo-Ríos LE, Tusié-Luna MT. Domínguez-López A, et al. JOP. 2005 May 10;6(3):238-45. JOP. 2005. PMID: 15883474
30 results