272 results on '"Mohand‐Saïd, 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. Author Correction: The development of white matter structural changes during the process of deterioration of the visual field
10. Cystoid maculopathy is a frequent feature of Cohen syndrome-associated retinopathy
11. Outer Retinal Alterations Associated With Visual Outcomes in Best Vitelliform Macular Dystrophy
12. Vision-Related Quality of Life in Patients with Diabetic Macular Edema Treated with Intravitreal Aflibercept: The AQUA Study
13. Phenotypic Characteristics of a French Cohort of Patients with X-Linked Retinoschisis
14. Longitudinal Changes of Fixation Location and Stability Within 12 Months in Stargardt Disease: ProgStar Report No. 12
15. Adapted Surgical Procedure for Argus II Retinal Implantation: Feasibility, Safety, Efficiency, and Postoperative Anatomic Findings
16. Full-field electroretinography, visual acuity and visual fields in Usher syndrome: a multicentre European study
17. Odysight: A Mobile Medical Application Designed for Remote Monitoring—A Prospective Study Comparison with Standard Clinical Eye Tests
18. Impact of Retinitis Pigmentosa on Quality of Life, Mental Health, and Employment Among Young Adults
19. PHENOTYPIC CHARACTERISTICS OF ROD–CONE DYSTROPHY ASSOCIATED WITH MYO7A MUTATIONS IN A LARGE FRENCH COHORT
20. X-Linked Retinoschisis
21. Normal Retina Releases a Diffusible Factor Stimulating Cone Survival in the Retinal Degeneration Mouse
22. Visual Acuity Loss and Associated Risk Factors in the Retrospective Progression of Stargardt Disease Study (ProgStar Report No. 2)
23. Clinical Characteristics and Risk Factors of Extensive Macular Atrophy with Pseudodrusen: The EMAP Case-Control National Clinical Trial
24. Increased functional connectivity between language and visually deprived areas in late and partial blindness
25. The development of white matter structural changes during the process of deterioration of the visual field
26. Reading Visual Braille with a Retinal Prosthesis
27. X-Linked Retinoschisis
28. Cone Survival: Identification of RdCVF
29. Functional and high-resolution retinal imaging monitoring photoreceptor damage in acute macular neuroretinopathy
30. Extensive myelinated retinal nerve fibres and bilateral foveal hypoplasia: A specific clinical entity
31. Computerized biofeedback to characterize Pupil Cycle Time (PCT) in neuropathies and retinopathies
32. Rods Produce a Diffusible Factor Promoting Cone Photoreceptor Survival In Vivo and in Vitro
33. Genetic Reactivation of Cone Photoreceptors Restores Visual Responses in Retinitis Pigmentosa
34. Reorganization of early visual cortex functional connectivity following selective peripheral and central visual loss
35. Retinal Phenotype of Patients with CLRN1-Associated Usher 3A Syndrome in French Light4Deaf Cohort
36. Novel TTLL5 Variants Associated with Cone-Rod Dystrophy and Early-Onset Severe Retinal Dystrophy
37. Mutations in IFT172 cause isolated retinal degeneration and Bardet–Biedl syndrome
38. Short postural training session improves stability in patients with age-related macular degeneration
39. Mutated CCDC51 Coding for a Mitochondrial Protein, MITOK Is a Candidate Gene Defect for Autosomal Recessive Rod-Cone Dystrophy
40. CNGB1 ‐related rod‐cone dystrophy: A mutation review and update
41. Management of a case of Enhanced S-cone syndrome with massive foveoschisis treated with pars plana vitrectomy with silicone oil tamponade
42. WDR34, a candidate gene for non-syndromic rod-cone dystrophy
43. Cystoid maculopathy is a frequent feature of Cohen syndrome-associated retinopathy
44. CHM mutation spectrum and disease: An update at the time of human therapeutic trials
45. The familial dementia gene revisited: a missense mutation revealed by whole-exome sequencing identifies ITM2B as a candidate gene underlying a novel autosomal dominant retinal dystrophy in a large family
46. CRB1 mutations in inherited retinal dystrophies
47. RP1 and autosomal dominant rod–cone dystrophy: Novel mutations, a review of published variants, and genotype–phenotype correlation
48. A Splice Variant in SLC16A8 Gene Leads to Lactate Transport Deficit in Human iPS Cell-Derived Retinal Pigment Epithelial Cells
49. The Search for Rod-Dependent Cone Viability Factors, Secreted Factors Promoting Cone Viability
50. Novel C2orf71 mutations account for ∽1% of cases in a large French arRP cohort
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