Showing results (31-40 of 39) with videos related to
Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
Clinical Endocrinology|March 9, 2022
Height and body mass index in molecularly confirmed Silver-Russell syndrome and the long-term effects of growth hormone treatmentOluwakemi Lokulo-Sodipe, Eloïse Giabicani, Ana P M Canton, et al.Brain : a Journal of Neurology|February 23, 2007
A splice site mutation in the murine Opa1 gene features pathology of autosomal dominant optic atrophyMarcel V Alavi, Stefanie Bette, Simone Schimpf, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 21, 2009
Loss of the cholesterol-binding protein prominin-1/CD133 causes disk dysmorphogenesis and photoreceptor degenerationSerena Zacchigna, Hideyasu Oh, Michaela Wilsch-Bräuninger, et al.Human Molecular Genetics|March 8, 2006
Mpp4 recruits Psd95 and Veli3 towards the photoreceptor synapseWendy M Aartsen, Albena Kantardzhieva, Jan Klooster, et al.Brain : a Journal of Neurology|June 28, 2014
Pure and syndromic optic atrophy explained by deep intronic OPA1 mutations and an intralocus modifierTobias Bonifert, Kathrin N Karle, Felix Tonagel, et al.Vision Research|September 29, 2005
In vivo confocal imaging of the retina in animal models using scanning laser ophthalmoscopyMathias W Seeliger, Susanne C Beck, Naira Pereyra-Muñoz, et al.Journal of Medical Genetics|September 21, 2023
Diagnostic genome sequencing improves diagnostic yield: a prospective single-centre study in 1000 patients with inherited eye diseasesNicole Weisschuh, Pascale Mazzola, Theresia Zuleger, et al.BMJ Open|March 3, 2016
Treatment of optic neuritis with erythropoietin (TONE): a randomised, double-blind, placebo-controlled trial-study protocolRicarda Diem, Fanni Molnar, Flemming Beisse, et al.Brain Communications|May 31, 2021
Dominant ACO2 mutations are a frequent cause of isolated optic atrophyMajida Charif, Naïg Gueguen, Marc Ferré, et al.Pageof 4