655 results on '"Webster, Andrew"'
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2. Non‐syndromic retinal dystrophy associated with biallelic variation of SUMF1 and reduced leukocyte sulfatase activity
3. Enhanced Learning and Memory in Patients with CRB1 Retinopathy
4. Neuropathy target esterase activity defines phenotypes among PNPLA6 disorders
5. Sex Distributions in Non-ABCA4 Autosomal Macular Dystrophies
6. Phenotyping and genotyping inherited retinal diseases: Molecular genetics, clinical and imaging features, and therapeutics of macular dystrophies, cone and cone-rod dystrophies, rod-cone dystrophies, Leber congenital amaurosis, and cone dysfunction syndromes
7. RP2-Associated X-linked Retinopathy: Clinical Findings, Molecular Genetics, and Natural History in a Large Cohort of Female Carriers
8. Pasteurella multocida
9. Quantification of Fundus Autofluorescence Features in a Molecularly Characterized Cohort of More Than 3000 Inherited Retinal Disease Patients from the United Kingdom
10. Congenital Stationary Night Blindness Structure, Function and Genotype–Phenotype Correlations in a Cohort of 122 Patients
11. IQCB1 (NPHP5)-retinopathy: Clinical and Genetic Characterization and Natural History
12. Visual Acuity by Decade in 139 Males with RPGR-Associated Retinitis Pigmentosa
13. PHYH c.678+5G>T Leads to In-Frame Exon Skipping and Is Associated With Attenuated Refsum Disease
14. Genetics, Clinical Characteristics, and Natural History of PDE6B-Associated Retinal Dystrophy
15. IMPG2-Related Maculopathy
16. Discrepancies in central foveal intensity with different autofluorescence modalities in CNGB3‐associated achromatopsia and correlation with integrity of ellipsoid zone on optical coherence tomography
17. Localised loss of sheen in Optos pseudocolour images in Oguchi disease following prior short wavelength autofluorescence imaging
18. Best Vitelliform Macular Dystrophy Natural History Study Report 1: Clinical Features and Genetic Findings.
19. Mutations in SAMD7 cause autosomal-recessive macular dystrophy with or without cone dysfunction
20. Spectrum of Genetic Variants in the Most Common Genes Causing Inherited Retinal Disease in a Large Molecularly Characterized United Kingdom Cohort
21. Hyperreflectivity of the outer portion of the outer nuclear layer seen on optical coherence tomography in some cases of NR2E3‐associated retinopathy
22. Ireland’s Heritage and the Production of Knowledge in Historical Archaeology
23. Rare disease gene association discovery from burden analysis of the 100,000 Genomes Project data
24. Estimating the burden of clinically significant Staphylococcus aureus infections and predictors for hospitalization for skin and soft tissue infections, Fulton County, GA, 2017
25. Detailed Clinical, Ophthalmic, and Genetic Characterization of ADGRV1-Associated Usher Syndrome
26. Coats-like Vasculopathy in Inherited Retinal Disease
27. 1226. Differences in diagnosis and procedure codes used among 5 Veterans Affairs telehealth antibiotic stewardship services
28. 2195. Impact of Optimizing Urine Culture Susceptibility Reports on Prescribing of Antimicrobials in Outpatients at the Atlanta VA Health Care System (AVAHCS)
29. Cone-driven strong flash electroretinograms in healthy adults: Prevalence of negative waveforms
30. Prognostication in Stargardt Disease Using Fundus Autofluorescence: Improving Patient Care
31. KCNV2-associated retinopathy: genotype–phenotype correlations –KCNV2study group report 3
32. RBP3-retinopathy - inherited high myopia and retinal dystrophy: Genetic Characterization, Natural History, and Deep Phenotyping
33. CERKL-Associated Retinal Dystrophy
34. Introduction: A Multidisciplinary Approach to the Digital Landscape
35. Introduction
36. Section 5: Regulation and Governance
37. Continental bookends—the arrival and departure of the Jurassic Sea in southern England
38. Collapsing centre
39. The battle of London
40. Introduction
41. Allies of yesterday
42. Conclusion
43. Missed opportunity
44. An opening clash
45. Security is the guardian of peace
46. Alternative paths
47. Enfin désarmement
48. The problems of 1930
49. Annus terribilis
50. The trials of victory
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