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Journal of Ophthalmology|January 15, 2011
An update on the genetics of usher syndromeJosé M Millán, Elena Aller, Teresa Jaijo, et al.Journal of Neuroimmunology|October 31, 2007
TLR4 haplotypes in multiple sclerosis: a case-control study in the Spanish populationElena Urcelay, Fiona Blanco-Kelly, Virginia de Las Heras, et al.Frontiers in Genetics|July 15, 2026
Case report: Characterization of a patient with novel biallelic variants in GTF3C3 and comprehensive review of previously reported casesLucía López-López, Beatriz González Giráldez, Yolanda Benítez, et al.Genes|March 6, 2021
Prevalent ALMS1 Pathogenic Variants in Spanish Alström PatientsBrais Bea-Mascato, Carlos Solarat, Irene Perea-Romero, et al.Investigative Ophthalmology & Visual Science|November 15, 2019
Expanding the Genetic Landscape of Usher-Like PhenotypesCarla Fuster-García, Gema García-García, Teresa Jaijo, et al.BMC Medical Genetics|January 8, 2017
New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case reportFiona Blanco-Kelly, Luciana Rodrigues-Jacy da Silva, Iker Sanchez-Navarro, et al.Molecular Vision|June 28, 2012
Genotyping microarray: mutation screening in Spanish families with autosomal dominant retinitis pigmentosaFiona Blanco-Kelly, María García-Hoyos, Marta Cortón, et al.International Journal of Molecular Sciences|January 21, 2023
Prioritization of New Candidate Genes for Rare Genetic Diseases by a Disease-Aware Evaluation of Heterogeneous Molecular NetworksLorena de la Fuente, Marta Del Pozo-Valero, Irene Perea-Romero, et al.JAMA Ophthalmology|November 7, 2014
Clinical aspects of Usher syndrome and the USH2A gene in a cohort of 433 patientsFiona Blanco-Kelly, Teresa Jaijo, Elena Aller, et al.Molecular Vision|October 30, 2014
Novel deletions involving the USH2A gene in patients with Usher syndrome and retinitis pigmentosaGema García-García, Elena Aller, Teresa Jaijo, et al.Pageof 8