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422 results on '"Lotery, Andrew J."'

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4. Comprehensive functional characterization of complement factor I rare variant genotypes identified in the SCOPE geographic atrophy cohort

5. Central serous chorioretinopathy: An evidence-based treatment guideline

6. Periodontitis and Outer Retinal Thickness: a Cross-Sectional Analysis of the United Kingdom Biobank Cohort

7. Large-scale multitrait genome-wide association analyses identify hundreds of glaucoma risk loci

12. IMPG2-Related Maculopathy

17. Exploring healthy retinal aging with deep learning

18. Genome-wide meta-analysis identifies 22 loci for normal tension glaucoma with significant overlap with high tension glaucoma.

26. Initial results from a first-in-human gene therapy trial on X-linked retinitis pigmentosa caused by mutations in RPGR

28. Central serous chorioretinopathy: Towards an evidence-based treatment guideline

29. Vision-Related Quality of Life in Patients with Diabetic Macular Edema Treated with Intravitreal Aflibercept: The AQUA Study

36. Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

41. Clustering disease trajectories in contrastive feature space for biomarker discovery in age-related macular degeneration

42. UK Biobank retinal imaging grading: methodology, baseline characteristics and findings for common ocular diseases

44. Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

46. Beyond the Complement Cascade: Insights into Systemic Immunosenescence and Inflammaging in Age-Related Macular Degeneration and Current Barriers to Treatment.

47. The COVID-19 Pandemic and Ophthalmic Care:A Qualitative Study of Patients with Neovascular Age-Related Macular Degeneration (nAMD)

49. New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics

50. Retinal gene therapy in X-linked retinitis pigmentosa caused by mutations in RPGR: Results at 6 months in a first in human clinical trial

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