250 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. Faster Sensitivity Loss around Dense Scotomas than for Overall Macular Sensitivity in Stargardt Disease: ProgStar Report No. 14
6. Author Correction: The development of white matter structural changes during the process of deterioration of the visual field
7. Cystoid maculopathy is a frequent feature of Cohen syndrome-associated retinopathy
8. Vision-Related Quality of Life in Patients with Diabetic Macular Edema Treated with Intravitreal Aflibercept: The AQUA Study
9. Adapted Surgical Procedure for Argus II Retinal Implantation: Feasibility, Safety, Efficiency, and Postoperative Anatomic Findings
10. Full-field electroretinography, visual acuity and visual fields in Usher syndrome: a multicentre European study
11. Odysight: A Mobile Medical Application Designed for Remote Monitoring—A Prospective Study Comparison with Standard Clinical Eye Tests
12. X-Linked Retinoschisis
13. The development of white matter structural changes during the process of deterioration of the visual field
14. PHENOTYPIC CHARACTERISTICS OF ROD–CONE DYSTROPHY ASSOCIATED WITH MYO7A MUTATIONS IN A LARGE FRENCH COHORT
15. Normal Retina Releases a Diffusible Factor Stimulating Cone Survival in the Retinal Degeneration Mouse
16. Reading Visual Braille with a Retinal Prosthesis
17. X-Linked Retinoschisis
18. Extensive myelinated retinal nerve fibres and bilateral foveal hypoplasia: A specific clinical entity
19. Cone Survival: Identification of RdCVF
20. Functional and high-resolution retinal imaging monitoring photoreceptor damage in acute macular neuroretinopathy
21. Computerized biofeedback to characterize Pupil Cycle Time (PCT) in neuropathies and retinopathies
22. Rods Produce a Diffusible Factor Promoting Cone Photoreceptor Survival In Vivo and in Vitro
23. Retinal Phenotype of Patients with CLRN1-Associated Usher 3A Syndrome in French Light4Deaf Cohort
24. Reorganization of early visual cortex functional connectivity following selective peripheral and central visual loss
25. Novel TTLL5 Variants Associated with Cone-Rod Dystrophy and Early-Onset Severe Retinal Dystrophy
26. Mutations in IFT172 cause isolated retinal degeneration and Bardet–Biedl syndrome
27. Mutated CCDC51 Coding for a Mitochondrial Protein, MITOK Is a Candidate Gene Defect for Autosomal Recessive Rod-Cone Dystrophy
28. CNGB1 ‐related rod‐cone dystrophy: A mutation review and update
29. Management of a case of Enhanced S-cone syndrome with massive foveoschisis treated with pars plana vitrectomy with silicone oil tamponade
30. Short postural training session improves stability in patients with age-related macular degeneration
31. WDR34, a candidate gene for non-syndromic rod-cone dystrophy
32. Cystoid maculopathy is a frequent feature of Cohen syndrome-associated retinopathy
33. 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
34. CHM mutation spectrum and disease: An update at the time of human therapeutic trials
35. Extensive myelinated retinal nerve fibres and bilateral foveal hypoplasia: A specific clinical entity.
36. A Splice Variant in SLC16A8 Gene Leads to Lactate Transport Deficit in Human iPS Cell-Derived Retinal Pigment Epithelial Cells
37. Improved performance and safety from Argus II retinal prosthesis post‐approval study in France
38. WDR34 , a candidate gene for non‐syndromic rod‐cone dystrophy
39. CRB1 mutations in inherited retinal dystrophies
40. RP1 and autosomal dominant rod–cone dystrophy: Novel mutations, a review of published variants, and genotype–phenotype correlation
41. The Search for Rod-Dependent Cone Viability Factors, Secreted Factors Promoting Cone Viability
42. Novel C2orf71 mutations account for ∽1% of cases in a large French arRP cohort
43. An Unusual Retinal Phenotype Associated With a Novel Mutation in RHO
44. Peripapillary Sparing With Near Infrared Autofluorescence Correlates With Electroretinographic Findings in Patients With Stargardt Disease
45. EYS Is a Major Gene for Rod-cone Dystrophies in France
46. Improved performance and safety from Argus II retinal prosthesis post‐approval study in France.
47. The aging of the retina
48. Development and application of a next-generation-sequencing (NGS) approach to detect known and novel gene defects underlying retinal diseases
49. Phenotype Analysis of Retinal Dystrophies in Light of the Underlying Genetic Defects: Application to Cone and Cone-Rod Dystrophies
50. Longitudinal Clinical Follow-up and Genetic Spectrum of Patients With Rod-Cone Dystrophy Associated With Mutations inPDE6AandPDE6B
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