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Journal of Hypertension|October 23, 2013
Early predictors of gestational hypertension in a low-risk cohort. Results of a pilot studyNieves Martell-Claros, Fiona Blanco-Kelly, María Abad-Cardiel, et al.Stem Cell Research|February 18, 2018
Generation of a human iPSC line from a patient with congenital glaucoma caused by mutation in CYP1B1 geneArantxa Bolinches-Amorós, Dunja Lukovic, Ana Artero Castro, et al.Molecular Vision|June 13, 2022
Novel homozygous mutations in the transcription factor NRL cause non-syndromic retinitis pigmentosaMohammed E El-Asrag, Marta Corton, Martin McKibbin, et al.Investigative Ophthalmology & Visual Science|April 30, 2020
Retinal Structure in RPE65-Associated Retinal DystrophyNeruban Kumaran, Michalis Georgiou, James W B Bainbridge, et al.Ophthalmology|August 25, 2012
Identification of an RP1 prevalent founder mutation and related phenotype in Spanish patients with early-onset autosomal recessive retinitisAlmudena Avila-Fernandez, Marta Corton, Koji M Nishiguchi, et al.Investigative Ophthalmology & Visual Science|February 19, 2011
Further associations between mutations and polymorphisms in the ABCA4 gene: clinical implication of allelic variants and their role as protector/risk factorsJana Aguirre-Lamban, Juan José González-Aguilera, Rosa Riveiro-Alvarez, et al.European Journal of Ophthalmology|November 16, 2022
Application of multicolour reflectance imaging for the characterisation of inherited retinal disordersNatalia Lorenzana-Blanco, Belen Jimenez-Rolando, Blanca Garcia-Sandoval, et al.Orphanet Journal of Rare Diseases|February 6, 2013
High frequency of CRB1 mutations as cause of Early-Onset Retinal Dystrophies in the Spanish populationMarta Corton, Sorina D Tatu, Almudena Avila-Fernandez, et al.Journal of Medical Genetics|March 30, 2021
Activation of cryptic donor splice sites by non-coding and coding PAX6 variants contributes to congenital aniridiaMaria Tarilonte, Patricia Ramos, Jennifer Moya, et al.Tremor and Other Hyperkinetic Movements (New York, N.Y.)|September 11, 2023
The enduring enigma of sporadic chorea: A single center case seriesPedro J Garcia Ruiz, Lola Diaz Feliz, Cici E Feliz, et al.Pageof 8