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Documenta Ophthalmologica. Advances in Ophthalmology|November 7, 2007
Functional characteristics of patients with retinal dystrophy that manifest abnormal parafoveal annuli of high density fundus autofluorescence; a review and updateAnthony G Robson, Michel Michaelides, Zubin Saihan, et al.The Journal of Eukaryotic Microbiology|July 18, 2001
Phylogenetic position of the trichomonad parasite of turkeys, Histomonas meleagridis (Smith) Tyzzer, inferred from small subunit rRNA sequenceD Gerbod, V P Edgcomb, C Noël, et al.Journal of Neuroimmune Pharmacology : the Official Journal of the Society on Neuroimmune Pharmacology|August 23, 2014
Expression of the mannose receptor CD206 in HIV and SIV encephalitis: a phenotypic switch of brain perivascular macrophages with virus infectionGerard E Holder, Christopher M McGary, Edward M Johnson, et al.Neuroimage|December 19, 2017
Artificial scotoma estimation based on population receptive field mappingA Hummer, M Ritter, M Woletz, et al.Ophthalmology|October 13, 2009
Novel mutations and electrophysiologic findings in RGS9- and R9AP-associated retinal dysfunction (Bradyopsia)Michel Michaelides, Zheng Li, Naheed A Rana, et al.Investigative Ophthalmology & Visual Science|September 2, 2016
Phenotype and Progression of Retinal Degeneration Associated With Nullizigosity of ABCA4Ana Fakin, Anthony G Robson, Kaoru Fujinami, et al.Neuroimage|July 9, 2016
Eyetracker-based gaze correction for robust mapping of population receptive fieldsA Hummer, M Ritter, M Tik, et al.Human Genetics|April 24, 2010
Use of genome-wide SNP homozygosity mapping in small pedigrees to identify new mutations in VSX2 causing recessive microphthalmia and a semidominant inner retinal dystrophySibel Ugur Iseri, Alexander W Wyatt, Gudrun Nürnberg, et al.Investigative Ophthalmology & Visual Science|November 8, 2016
The Effect on Retinal Structure and Function of 15 Specific ABCA4 Mutations: A Detailed Examination of 82 Hemizygous PatientsAna Fakin, Anthony G Robson, John Pei-Wen Chiang, et al.Human Molecular Genetics|July 13, 2013
Molecular modeling indicates distinct classes of missense variants with mild and severe XLRS phenotypesYuri V Sergeev, Susan Vitale, Paul A Sieving, et al.Pageof 36