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1. Clinical spectrum of severe chronic central serous chorioretinopathy and outcome of photodynamic therapy

2. Clinical characteristics and long-term visual outcome of severe phenotypes of chronic central serous chorioretinopathy

3. Alteration of retinal layers in healthy subjects over 60 years of age until nonagenarians

4. Chronic central serous chorioretinopathy: long-term follow-up and vision-related quality of life

5. Neovascular age-related macular degeneration without drusen in the fellow eye: clinical spectrum and therapeutic outcome

7. A saturated map of common genetic variants associated with human height

8. Using human-induced pluripotent stem cells for modelling the blood-retinal-barrier on-a-chip

9. Metabolomics identifies lipoprotein subclasses and dietary metabolites that are associated with AMD: The EYE-RISK Consortium

10. Comparing the Efficacy of Bevacizumab and Ranibizumab in Patients with Diabetic Macular Edema (BRDME): The BRDME Study, a Randomized Trial

11. Integrating Metabolomics, Genomics, and Disease Pathways in Age-Related Macular Degeneration: The EYE-RISK Consortium

12. Development of a genotyping assay for AMD: the EYE-RISK Consortium

14. Genetic Risk Score has added value over initial clinical grading stage in predicting disease progression in patients with non-advanced age-related macular degeneration - the Muenster Aging and Retina Study (MARS)

17. Comparing the Efficacy of Bevacizumab and Ranibizumab in Patients with Retinal Vein Occlusion: The Bevacizumab to Ranibizumab in Retinal Vein Occlusions (BRVO) study, a Randomized Trial

18. Genome-wide association analyses identify two susceptibility loci for pachychoroid disease central serous chorioretinopathy.

19. Progression characteristics of ellipsoid zone loss in macular telangiectasia type 2

20. Pathway Analysis Integrating Genome-Wide and Functional Data Identifies PLCG2 as a Candidate Gene for Age-Related Macular Degeneration

21. Deep-intronic ABCA4 variants explain missing heritability in Stargardt disease and allow correction of splice defects by antisense oligonucleotides

22. Clinical Characterization of 66 Patients With Congenital Retinal Disease Due to the Deep-Intronic c.2991+11655A > G Mutation in CEP290

24. Non-syndromic retinitis pigmentosa

25. Whole-Exome Sequencing in Age-Related Macular Degeneration Identifies Rare Variants in COL8A1, a Component of Bruch's Membrane

26. The Spectrum of Structural and Functional Abnormalities in Female Carriers of Pathogenic Variants in the RPGR Gene

28. The Common ABCA4 Variant p.Asn1868Ile Shows Nonpenetrance and Variable Expression of Stargardt Disease When Present in trans With Severe Variants

30. Imaging protocols in clinical studies in advanced age-related macular degeneration: recommendations from classification of atrophy consensus meetings

31. Imaging Protocols in Clinical Studies in Advanced Age-Related Macular Degeneration

32. Aberrant leukocyte telomere length in Birdshot Uveitis

33. Diagnostic exome sequencing in 266 Dutch patients with visual impairment

34. Vergleich der Krankheits-Progression bei 'late-onset' Morbus Stargardt und altersabhängiger Makuladegeneration

36. Progression of Late-Onset Stargardt Disease

37. Pharmacogenetics in neovascular AMD: useful or useless?

38. The level of complement activation varies between the stages of AMD degeneration

39. GWAS study using DNA pooling strategy identifies association of variant rs4910623 in OR52B4 gene with anti-VEGF treatment response in age-related macular degeneration

40. A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants

45. The incidence of rhegmatogenous retinal detachment in the Netherlands: Dutch Rhegmatogenous Retinal Detachment Study Group

47. Late-Onset Stargardt disease

48. Benefits and risks of vitrectomy with epiretinal membrane peeling

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