David Rivera-De la Parra

Congenital Hereditary Endothelial Dystrophy Caused by SLC4A11 Mutations Progresses to Harboyan Syndrome

Salina Siddiqui, Juan Carlos Zenteno, Aine Rice et al. · Cornea · 2013 · 56 citations · Full text

Prevalence of high-risk alleles in the<i>LOXL1</i>gene and its association with pseudoexfoliation syndrome and exfoliation glaucoma in a Latin American population

Martha Jaimes, David Rivera-De la Parra, Antonio Miranda‐Duarte et al. · Ophthalmic Genetics · 2011 · 31 citations

A New<i>GJA1</i>(Connexin 43) Mutation Causing Oculodentodigital Dysplasia Associated to Uncommon Features

David Rivera-De la Parra, Juan Carlos Zenteno · Ophthalmic Genetics · 2007 · 20 citations

Developmental Anomaly, Developmental Biology, Mendelian Disorder +14

Triple A or Allgrove Syndrome. A Case Report with Ophthalmic Abnormalities and a Novel Mutation in the<i>AAAS</i>Gene

Cristina Villanueva‐Mendoza, Oswaldo Martínez-Guzmán, David Rivera-De la Parra et al. · Ophthalmic Genetics · 2009 · 19 citations

Identification of unsuspected Wolfram syndrome cases through clinical assessment and WFS1 gene screening in type 1 diabetes mellitus patients

María E. Blanco-Aguirre, David Rivera-De la Parra, Hugo Tapia-Garcia et al. · Gene · 2015 · 18 citations

Type 1, Wfs1 Gene, Inherited Metabolic Disease +6