Nelly Altamirano-Bustamante

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

María Luisa Ordóñez-Sánchez, Salvador Ramı́rez-Jiménez, Antonio Ulises López-Gutierrez et al. · Human Genetics · 1998 · 64 citations

Mexican Population, Mendelian Disorder, Genetic Disorder +10

Promoting networks between evidence-based medicine and values-based medicine in continuing medical education

Myriam M. Altamirano‐Bustamante, Nelly Altamirano-Bustamante, Alberto Lifshitz et al. · BMC Medicine · 2013 · 40 citations · Full text

Mutations in MODY genes are not common cause of early-onset type 2 diabetes in Mexican families.

Aarón Domínguez‐López, Ángel Miliar-García, Yayoi Segura-Kato et al. · PubMed · 2005 · 28 citations

Drug Development in Conformational Diseases: A Novel Family of Chemical Chaperones that Bind and Stabilise Several Polymorphic Amyloid Structures

Marquiza Sablón-Carrazana, I. González Fernández, Alberto Bencomo et al. · PLoS ONE · 2015 · 22 citations · Full text

Diabetes Drug Discovery: hIAPP1–37 Polymorphic Amyloid Structures as Novel Therapeutic Targets

Isaac Fernández-Gómez, Marquiza Sablón-Carrazana, Alberto Bencomo-Martínez et al. · Molecules · 2018 · 22 citations · Full text