Search

Your search keyword '"Sahel, José‐Alain"' showing total 2,036 results

Search Constraints

Start Over You searched for: Author "Sahel, José‐Alain" Remove constraint Author: "Sahel, José‐Alain"
2,036 results on '"Sahel, José‐Alain"'

Search Results

1. Freqformer: Frequency-Domain Transformer for 3-D Visualization and Quantification of Human Retinal Circulation

2. Coding and non-coding variants in the ciliopathy gene CFAP410 cause early-onset non-syndromic retinal degeneration.

3. BreakNet: Discontinuity-Resilient Multi-Scale Transformer Segmentation of Retinal Layers

4. Endpoints and Design for Clinical Trials in USH2A-Related Retinal Degeneration: Results and Recommendations From the RUSH2A Natural History Study

6. The AKT2/SIRT5/TFEB pathway as a potential therapeutic target in non-neovascular AMD

7. Splenic monocytes drive pathogenic subretinal inflammation in age-related macular degeneration

11. Diagnostic Quality Assessment of Fundus Photographs: Hierarchical Deep Learning with Clinically Significant Explanations

12. Static Perimetry in the Rate of Progression in USH2A-related Retinal Degeneration (RUSH2A) Study: Assessment Through 2 Years

13. Diffuse laser illumination for Maxwellian view Doppler holography of the retina

14. Randomized trial of bilateral gene therapy injection for m.11778G>A MT-ND4 Leber optic neuropathy

15. Indirect Comparison of Lenadogene Nolparvovec Gene Therapy Versus Natural History in Patients with Leber Hereditary Optic Neuropathy Carrying the m.11778G>A MT-ND4 Mutation.

16. Extensive macular atrophy with pseudodrusen-like appearance (EMAP) clinical characteristics, diagnostic criteria, and insights from allied inherited retinal diseases and age-related macular degeneration

20. Phase 1/2 AAV5-hRKp.RPGR (Botaretigene Sparoparvovec) Gene Therapy: Safety and Efficacy in RPGR-Associated X-Linked Retinitis Pigmentosa

21. Visual Acuity, Full-field Stimulus Thresholds, and Electroretinography for 4 Years in The Rate of Progression of USH2A-related Retinal Degeneration (RUSH2A) Study

25. Coagulase-negative staphylococcal endophthalmitis: clinical severity and outcomes based on speciation

27. Variants in UBAP1L lead to autosomal recessive rod-cone and cone-rod dystrophy

29. Natural history of patients with Leber hereditary optic neuropathy-results from the REALITY study.

30. Laser Doppler holography of the anterior segment for blood flow imaging, eye tracking, and transparency assessment

31. Non invasive live imaging of a novel retinal pigment epithelium stress model with Dynamic Full-Field Optical Coherence Tomography

32. Waveform analysis of human retinal and choroidal blood flow with laser Doppler holography

33. Choroidal vasculature imaging with laser Doppler holography

40. Long-Term Follow-Up After Unilateral Intravitreal Gene Therapy for Leber Hereditary Optic Neuropathy: The RESTORE Study.

42. Tackling the Challenges of Product Development Through a Collaborative Rare Disease Network: The Foundation Fighting Blindness Consortium

43. Intravitreal Gene Therapy vs. Natural History in Patients With Leber Hereditary Optic Neuropathy Carrying the m.11778G>A ND4 Mutation: Systematic Review and Indirect Comparison.

44. scAAVengr, a transcriptome-based pipeline for quantitative ranking of engineered AAVs with single-cell resolution

45. Dynamic full-field optical coherence tomography: 3D live-imaging of retinal organoids

46. Baseline Visual Field Findings in the RUSH2A Study: Associated Factors and Correlation With Other Measures of Disease Severity

48. Safety of Lenadogene Nolparvovec Gene Therapy Over 5 Years in 189 Patients With Leber Hereditary Optic Neuropathy

49. Shedding light on myopia by studying complete congenital stationary night blindness

50. Pathology of the Retina and Vitreous

Catalog

Books, media, physical & digital resources