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Ophthalmic Genetics|December 3, 2025
Short stature, optic atrophy, and Pelger-Huët anomaly (SOPH) syndrome: report of a case lacking neutrophil morphologic changes and review of literatureEmily H Jung, Michael Zhu, Anna Duemler, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|February 16, 2011
Autosomal recessive best vitelliform macular dystrophy: report of a family and management of early-onset neovascular complicationsAlessandro Iannaccone, Natalie C Kerr, Tyson R Kinnick, et al.Molecular Vision|October 26, 2007
Identification of two novel mutations in families with X-linked ocular albinismAlessandro Iannaccone, Kevin T Gallaher, Janda Buchholz, et al.Documenta Ophthalmologica. Advances in Ophthalmology|May 4, 2007
Fundus albipunctatus in a 6-year old girl due to compound heterozygous mutations in the RDH5 geneAlessandro Iannaccone, Salvatore A Tedesco, Kevin T Gallaher, et al.Investigative Ophthalmology & Visual Science|August 4, 2018
Murine Retinal Citrullination Declines With Age and is Mainly Dependent on Peptidyl Arginine Deiminase 4 (PAD4)T J Hollingsworth, Marko Z Radic, Sarka Beranova-Giorgianni, et al.Molecular Vision|October 26, 2022
Identification of numerous novel disease-causing variants in patients with inherited retinal diseases, combining careful clinical-functional phenotyping with systematic, broad NGS panel-based genotypingPriya R Gupta, Wajiha Kheir, Bo Peng, et al.Journal of Clinical Medicine|January 30, 2021
Interspecies Correlations between Human and Mouse NR2E3-Associated Recessive DiseaseAlessandro Iannaccone, Emily Brabbit, Christiaan Lopez-Miro, et al.Investigative Ophthalmology & Visual Science|January 26, 2007
Age-related decline in VIP-positive parasympathetic nerve fibers in the human submacular choroidMonica M Jablonski, Alessandro Iannaccone, Drew H Reynolds, et al.Investigative Ophthalmology & Visual Science|February 20, 2014
Diagnostic sensitivity and specificity of dark adaptometry for detection of age-related macular degenerationGregory R Jackson, Ingrid U Scott, Ivana K Kim, et al.American Journal of Medical Genetics. Part A|January 18, 2005
Clinical evidence of decreased olfaction in Bardet-Biedl syndrome caused by a deletion in the BBS4 geneAlessandro Iannaccone, Kirk Mykytyn, Antonio M Persico, et al.Pageof 8