211 results on '"Mohand-Said, Saddek"'
Search Results
2. Variants in UBAP1L lead to autosomal recessive rod-cone and cone-rod dystrophy
3. Development and Validation of a Novel Mobility Test for Rod-Cone Dystrophies: From Reality to Virtual Reality
4. Pegcetacoplan for the treatment of geographic atrophy secondary to age-related macular degeneration (OAKS and DERBY): two multicentre, randomised, double-masked, sham-controlled, phase 3 trials
5. Three‐Year Safety Results of SAR422459 (EIAV‐ABCA4) Gene Therapy in Patients With ABCA4‐Associated Stargardt Disease: An Open‐Label Dose‐Escalation Phase I/IIa Clinical Trial, Cohorts 1‐5
6. Assessing Photoreceptor Status in Retinal Dystrophies: From High-Resolution Imaging to Functional Vision
7. Photovoltaic Restoration of Central Vision in Atrophic Age-Related Macular Degeneration
8. Faster Sensitivity Loss around Dense Scotomas than for Overall Macular Sensitivity in Stargardt Disease: ProgStar Report No. 14
9. Near-infrared fundus autofluorescence alterations correlate with swept-source optical coherence tomography angiography findings in patients with retinitis pigmentosa
10. Outer Retinal Alterations Associated With Visual Outcomes in Best Vitelliform Macular Dystrophy
11. Vision-Related Quality of Life in Patients with Diabetic Macular Edema Treated with Intravitreal Aflibercept: The AQUA Study
12. Phenotypic Characteristics of a French Cohort of Patients with X-Linked Retinoschisis
13. Longitudinal Changes of Fixation Location and Stability Within 12 Months in Stargardt Disease: ProgStar Report No. 12
14. Adapted Surgical Procedure for Argus II Retinal Implantation: Feasibility, Safety, Efficiency, and Postoperative Anatomic Findings
15. Impact of Retinitis Pigmentosa on Quality of Life, Mental Health, and Employment Among Young Adults
16. X-Linked Retinoschisis
17. Normal Retina Releases a Diffusible Factor Stimulating Cone Survival in the Retinal Degeneration Mouse
18. Visual Acuity Loss and Associated Risk Factors in the Retrospective Progression of Stargardt Disease Study (ProgStar Report No. 2)
19. Clinical Characteristics and Risk Factors of Extensive Macular Atrophy with Pseudodrusen: The EMAP Case-Control National Clinical Trial
20. Increased functional connectivity between language and visually deprived areas in late and partial blindness
21. AUTOSOMAL DOMINANT VITREORETINOCHOROIDOPATHY: When Molecular Genetic Testing Helps Clinical Diagnosis
22. Development and validation of a novel mobility test for IRDs, from reality to virtual reality
23. Reading Visual Braille with a Retinal Prosthesis
24. X-Linked Retinoschisis
25. Cone Survival: Identification of RdCVF
26. Retrospective Natural History Study of RPGR-Related Cone- and Cone-Rod Dystrophies While Expanding the Mutation Spectrum of the Disease
27. Rods Produce a Diffusible Factor Promoting Cone Photoreceptor Survival In Vivo and in Vitro
28. Genetic Reactivation of Cone Photoreceptors Restores Visual Responses in Retinitis Pigmentosa
29. Pegcetacoplan for the treatment of geographic atrophy secondary to age-related macular degeneration (OAKS and DERBY): two multicentre, randomised, double-masked, sham-controlled, phase 3 trials
30. One minute Multiple Pupillary Frequency Tagging test to assess visual field defects
31. Reactivating the phototransduction cascade by universally applicable gene therapy preserves retinal function in Rod-Cone dystrophy
32. Functional rescue of cone photoreceptors in retinitis pigmentosa
33. Characteristics of Retinitis Pigmentosa Associated with ADGRV1 and Comparison with USH2A in Patients from a Multicentric Usher Syndrome Study Treatrush
34. NMNAT1 mutations cause Leber congenital amaurosis
35. Mutations in TRPM1 are a common cause of complete congenital stationary night blindness
36. A novel DFNB31 mutation associated with Usher type 2 syndrome showing variable degrees of auditory loss in a consanguineous Portuguese family
37. Healthy and pathological visual aging in a French follow-up cohort study
38. DEEP PHENOTYPING AND FURTHER INSIGHTS INTO ITM2B-RELATED RETINAL DYSTROPHY
39. Simultaneous Perception of Prosthetic and Natural Vision in AMD Patients
40. Retinal Phenotype of Patients With Isolated Retinal Degeneration Due to CLN3 Pathogenic Variants in a French Retinitis Pigmentosa Cohort
41. Faster Sensitivity Loss around Dense Scotomas than for Overall Macular Sensitivity in Stargardt Disease: ProgStar Report No. 14
42. Effect of Visual Search Training on Saccades in Age-related Macular Degeneration Subjects
43. An unusual retinal phenotype associated with a novel mutation in RHO
44. Rétinopathies pigmentaires : de la thérapie cellulaire à la signalisation intercellulaire
45. Chapter 47 Rod-cone interdependence: implications for therapy of photoreceptor cell diseases
46. Inherited retinal degenerations: therapeutic prospects
47. The aging of the retina
48. Differential Proteomic Analysis of the Mouse Retina: The Induction of Crystallin Proteins by Retinal Degeneration in the rd1 Mouse
49. Selective Transplantation of Rods Delays Cone Loss in a Retinitis Pigmentosa Model
50. Vision-Related Quality of Life in Patients with Diabetic Macular Edema Treated with Intravitreal Aflibercept
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