287 results on '"Greenstein, Vivienne"'
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2. Correlations of Full-Field Stimulus Threshold With Functional and Anatomical Outcome Measurements in Advanced Retinitis Pigmentosa
3. Qualitative and quantitative comparison of ERGs with contact lens and adhesive skin electrodes
4. Structure–function analysis for macular surgery in patients with coexisting glaucoma
5. Foveolar thickness as potential standardized structural outcome measurement in studies of Bietti crystalline dystrophy
6. Monitoring Lesion Area Progression in Stargardt Disease: A Comparison of En Face Optical Coherence Tomography and Fundus Autofluorescence
7. Multimodal analysis of the Preferred Retinal Location and the Transition Zone in patients with Stargardt Disease
8. ACUTE ZONAL OCCULT OUTER RETINOPATHY: Structural and Functional Analysis Across the Transition Zone Between Healthy and Diseased Retina
9. Recessive Stargardt disease phenocopying hydroxychloroquine retinopathy
10. Choroideremia Carriers: Dark-Adapted Perimetry and Retinal Structures
11. Fundus-driven perimetry (microperimetry) compared to conventional static automated perimetry: similarities, differences, and clinical applications
12. A comparison of structural and functional changes in patients screened for hydroxychloroquine retinopathy
13. Progressive Constriction of the Hyperautofluorescent Ring in Retinitis Pigmentosa
14. Comparisons Among Optical Coherence Tomography and Fundus Autofluorescence Modalities as Measurements of Atrophy in ABCA4-Associated Disease
15. Structure–function analysis for macular surgery in patients with coexisting glaucoma
16. Rapid retinal functional testing
17. G1961E mutant allele in the Stargardt disease gene ABCA4 causes bull's eye maculopathy
18. New syndrome with retinitis pigmentosa is caused by nonsense mutations in retinol dehydrogenase RDH11
19. CNGB1 ‐related rod‐cone dystrophy: A mutation review and update
20. Abnormal multifocal ERG findings in patients with normal-appearing retinal anatomy
21. Multifocal visual evoked potential and automated perimetry abnormalities in strabismic amblyopes
22. A comparison of multifocal ERG and frequency domain OCT changes in patients with abnormalities of the retina
23. A method to detect progression of glaucoma using the multifocal visual evoked potential technique
24. Novel electrophysiological instrument for rapid and objective assessment of magnocellular deficits associated with glaucoma
25. A comparison of multifocal and conventional visual evoked potential techniques in patients with optic neuritis/multiple sclerosis
26. Scotopic sensitivity and color vision with a blue-light-absorbing intraocular lens
27. Long-Term Maintenance of Vision and Resolution of Vitelliform Lesions with Systemic Phosphodiesterase 5/6 Treatment (Sildenafil)
28. Test–retest reliability of the multifocal electroretinogram and Humphrey visual fields in patients with retinitis pigmentosa
29. Evaluation of multimodal imaging in carriers of X-linked retinitis pigmentosa
30. A study of factors affecting the human cone photoreceptor density measured by adaptive optics scanning laser ophthalmoscope
31. Optical Gap Biomarker in Cone-Dominant Retinal Dystrophy
32. Quantitative Fundus Autofluorescence in HCQ Retinopathy
33. Visual field expansion after visual restoration therapy
34. Chapter 15 Acquired retinopathies
35. The multifocal visual evoked potential: An objective measure of visual fields?
36. A Method for Comparing Electrophysiological, Psychophysical, and Structural Measures of Glaucomatous Damage
37. Visual Field Defects and Multifocal Visual Evoked Potentials: Evidence of a Linear Relationship
38. Early-Stage Vision and Schizophrenia
39. Retinal Pigment Epithelial Dysfunction in Patients With Pigment Dispersion Syndrome: Implications for the Theory of Pathogenesis
40. Dysfunction of Early-Stage Visual Processing in Schizophrenia
41. Multifocal VEP and ganglion cell damage: applications and limitations for the study of glaucoma
42. Clinical and genetic findings in Italian patients with sector retinitis pigmentosa.
43. Multimodal analysis of the Preferred Retinal Location and the Transition Zone with macular atrophy in Patients with Stargardt Disease
44. A Comparison of S Cone Pathway Sensitivity Loss in Patients with Diabetes and Retinitis Pigmentosa
45. A Psychophysical Technique for Testing Explanations of Sensitivity Loss Due to Retinal Disease
46. A Comparison of En Face Optical Coherence Tomography and Fundus Autofluorescence in Stargardt Disease
47. Quantitative Fundus Autofluorescence and Optical Coherence Tomography inABCA4Carriers
48. Cone function in congenital nyctalopia
49. Recessive Stargardt disease phenocopying hydroxychloroquine retinopathy
50. Near-Infrared Autofluorescence: Its Relationship to Short-Wavelength Autofluorescence and Optical Coherence Tomography in Recessive Stargardt Disease
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