Results 141 to 147 of about 971 (147)

The absence of fundus abnormalities in Stargardt disease

Graefe's Archive for Clinical and Experimental Ophthalmology, 2019
Stanley Lambertus, Carel B Hoyng, Jeroen Klevering   +2 more
exaly  

Natural History of Autosomal Recessive Stargardt Disease in Untreated EyesA Systematic Review and Meta-analysis of Study- and Individual-Level Data

Ophthalmology, 2019
Holly K Grossetta Nardini, Liangbo L. Shen, Lucian Del Priore   +2 more
exaly  

Highly Variable Disease Courses in Siblings with Stargardt Disease

Ophthalmology, 2019
Clara I Sánchez, Carel B Hoyng, Bart Liefers   +2 more
exaly  

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Frontiers in Genetics, 2019
Gezhi Xu, Qing Chang
exaly  

Visual Acuity Change over 12 Months in the Prospective Progression of Atrophy Secondary to Stargardt Disease (ProgStar) StudyProgStar Report Number 6

Ophthalmology, 2017
Xiangrong Kong, Michel Michaelides, Artur V Cideciyan   +2 more
exaly  

Generation of a compound heterozygous ABCA4 rat model with pathological features of STGD1 Open Access

Human Molecular Genetics
Nathalie Provost
exaly  

Study of Late-Onset Stargardt Type 1 DiseaseCharacteristics, Genetics, and Progression

Ophthalmology
Jeroen Pas, Carel B Hoyng, Frans P M Cremers   +2 more
exaly