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- The Effect of Light Deprivation in Patients with Stargardt Disease
- Treatment of Stargardt Disease with Dobesilate
- Volume 5 Issue 4
- Review Article GENE THERAPY for STARGARDT and OTHER ABCA4-RELATED DISEASES: LESSONS from the RPE65-LCA TRIALS
- Clinical and Molecular Characterization of Achromatopsia Patients: a Longitudinal Study
- Visual Loss of Uncertain Origin: Diagnostic Strategies
- Nerve Fibre Layer Loss in Diseases of the Outer Retinal Layer
- Stargardt's Disease
- Primary Focus: Blindness and Regeneration
- Dr S Anuradha Original Research Paper Ophthalmology Dr B Latha* Dr C Sony Shireesha Dr M Sushma
- The Socioeconomic Impact of Inherited Retinal Dystrophies (Irds) in the United Kingdom Retina International August 2019
- Central Serous Chorioretinopathy
- Stargardt's Disease: Clinical Presentation and Fundus
- Achromatopsia Achromatopsia Is a Rare Hereditary Vision Disorder
- Review Article Eye Disorders: Primary Hereditary Diseases of the Retina
- Christine N. Kay, MD Is a Vitreoretinal Specialist and Assistant Professor of Ophthalmology at the University of Florida
- Posterior Segment Retina
- Therapy Approaches for Stargardt Disease
- Stargardt Disease: Advances and Obstacles
- Precision Ophthalmology
- Stargardt Disease: Clinical Features, Molecular Genetics, Animal Models
- Case Report Comment
- (Part 1) – Overview and Assessment of Inherited Retinal Disease
- Inherited Retinal Diseases: Therapeutics, Clinical Trials and End Points—A Review
- An Overview of the Genetics of ABCA4 Retinopathies, an Evolving Story
- Inherited Retinal Diseases
- Gene Therapy for Usher Syndrome (And Other Treatments)
- The Absence of Fundus Abnormalities in Stargardt Disease
- Journal Highlights NEW FINDINGS from the PEER-REVIEWED LITERATURE
- Targeting the Visual Cycle: Dry Amd and Stargardt Disease
- Case of the Month – June 2021 Presented by Christian Sanfilippo, MD
- Blueprint Genetics Macular Dystrophy Panel
- Macular Dystrophies: Clinical and Imaging Features, Molecular
- Avellino Labs
- Detection Rate of Pathogenic Mutations in ABCA4 Using Direct
- Stargardt Disease Introduction
- Distinct Characteristics of Inferonasal Fundus Autofluorescence Patterns
- Gene and Cell Therapy for Blindness. Deniz Dalkara, Olivier Goureau, Katia Marazova, José-Alain Sahel
- EN Press Release STGD FPFV 20170126 (8) Clean
- Electrophysiological Findings in Stargardt's Fundus Flavimaculatus
- Novel Mutations in CRB1 and ABCA4 Genes Cause Leber Congenital Amaurosis and Stargardt Disease in a Swedish Family
- Inherited Retinal Degeneration: Genetics, Disease Characterization, and Outcome Measures
- Clinical FOCUS
- Association Between Visual Function and the Integrity of Residual
- Stargardt Disease Stargardt Disease Is the Most Common Form of Inherited Juvenile Macular Degeneration and It Affects the Portion of the Retina Known As the Macula
- Diagnosis and Management of Stargardt Disease
- Assessment of Fundus Auto Uorescence and Adaptive Optics
- Stargardt's Disease
- Comprehensive Analysis of Patients with Stargardt Macular Dystrophy Reveals New Genotype–Phenotype Correlations and Unexpected Diagnostic Revisions
- Stargardt Macular Degeneration
- Treatments for Dry Age-Related Macular Degeneration and Stargardt Disease: a Systematic Review
- Grand Rounds November 20, 2014
- Bright Spot on Geographic Atrophy Map
- Stargardt's Disease and Fundus Flavimaculatus: Evaluation of Morphologic Progression and Intrafamilial Co-Existence*
- Case Repor T
- Stem Cells in the Path of Light, from Corneal to Retinal Reconstruction
- Patient History for Retinitis Pigmentosa/Leber Congenital Amaurosis Testing
- An Epidemiological Approach for the Estimation of Disease Onset in Central Europe in Central and Peripheral Monogenic Retinal Dystrophies
- The Successful Management of Stargardt's Disease Using Topical
- Mystery Retina 2018: Interactive Discussion of Challenging Cases
- Genotypes Predispose Phenotypes—Clinical Features and Genetic Spectrum of ABCA4-Associated Retinal Dystrophies