28 results on '"Moosajee, Mariya"'
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2. Enhanced Learning and Memory in Patients with CRB1 Retinopathy
3. Inherited Optic Neuropathies: Real-World Experience in the Paediatric Neuro-Ophthalmology Clinic
4. Gene Augmentation of CHM Using Non-Viral Episomal Vectors in Models of Choroideremia
5. Foveal Hypoplasia in CRB1-Related Retinopathies
6. Oxidative and Endoplasmic Reticulum Stress Represent Novel Therapeutic Targets for Choroideremia
7. Nuclear Receptor Subfamily 2 Group E Member 3 (NR2E3): Role in Retinal Development and Disease
8. Identification of Novel Coloboma Candidate Genes through Conserved Gene Expression Analyses across Four Vertebrate Species
9. A Natural History Study of RP2-Related Retinopathy
10. Changes in Mitochondrial Size and Morphology in the RPE and Photoreceptors of the Developing and Ageing Zebrafish
11. The Natural History of CNGB1-Related Retinopathy: A Longitudinal Phenotypic Analysis
12. Investigating Biomarkers for USH2A Retinopathy Using Multimodal Retinal Imaging
13. Involvement of Oxidative and Endoplasmic Reticulum Stress in RDH12-Related Retinopathies
14. Prospective Study of the Phenotypic and Mutational Spectrum of Ocular Albinism and Oculocutaneous Albinism
15. Metabolism in the Zebrafish Retina
16. The Genetic and Clinical Features of FOXL2-Related Blepharophimosis, Ptosis and Epicanthus Inversus Syndrome
17. The Landscape of Non-Viral Gene Augmentation Strategies for Inherited Retinal Diseases
18. EPHA2 Segregates with Microphthalmia and Congenital Cataracts in Two Unrelated Families
19. Acceptability of Telegenetics for Families with Genetic Eye Diseases
20. Ocular Phenotype Associated with DYRK1A Variants
21. A Novel Splice-Site Variant in CACNA1F Causes a Phenotype Synonymous with Åland Island Eye Disease and Incomplete Congenital Stationary Night Blindness
22. Novel Biallelic Variants and Phenotypic Features in Patients with SLC38A8-Related Foveal Hypoplasia
23. From Transcriptomics to Treatment in Inherited Optic Neuropathies
24. Clinical Spectrum and Genetic Diagnosis of 54 Consecutive Patients Aged 0–25 with Bilateral Cataracts
25. Update on Gene Therapy Clinical Trials for Choroideremia and Potential Experimental Therapies
26. Longitudinal Study to Assess the Quantitative Use of Fundus Autofluorescence for Monitoring Disease Progression in Choroideremia
27. The Spectrum of PAX6 Mutations and Genotype-Phenotype Correlations in the Eye
28. The Molecular Basis of Human Anophthalmia and Microphthalmia.
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