582 results on '"MacDonald, Ian M."'
Search Results
2. Retinal dystrophy associated with Birt-Hogg-Dubé syndrome
3. Breaking bad news in ophthalmology: a pilot skills workshop for residents
4. Perspectives on Gene Therapy: Choroideremia Represents a Challenging Model for the Treatment of Other Inherited Retinal Degenerations.
5. Zebrafish and inherited photoreceptor disease: Models and insights
6. Macular spatial distribution of preserved autofluorescence in patients with choroideremia
7. The inner junction protein CFAP20 functions in motile and non-motile cilia and is critical for vision
8. Long anterior lens zonules in late-onset retinal degeneration
9. Choroideremia
10. Whole exome sequencing reveals putatively novel associations in retinopathies and drusen formation
11. Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics
12. Pseudoxanthoma elasticum and retinitis pigmentosa in a patient with a novel mutation in the ABCC6 gene.
13. Breaking bad news in ophthalmology: a pilot skills workshop for residents
14. Choroideremia
15. Recognizing and Mitigating Risk of Ophthalmic Regional Anesthesia
16. High-Resolution Images of Retinal Structure in Patients with ChoroideremiaHigh-Resolution Retinal Images in Choroideremia
17. Overcoming the Challenges to Clinical Development of X-Linked Retinitis Pigmentosa Therapies: Proceedings of an Expert Panel
18. AAV2-Mediated Gene Therapy for Choroideremia: 5-Year Results and Alternate Anti-sense Oligonucleotide Therapy
19. AA and DHA are decreased in paediatric AD/HD and inattention is ameliorated by increased plasma DHA
20. RETINAL PHENOTYPE IN A CASE OF LCHAD/TFP DEFICIENCY WITH LATE-STAGE DIAGNOSIS
21. Communicating the Promise for Ocular Gene Therapies: Challenges and Recommendations
22. Upward saccadic intrusions as the presenting feature for incomplete congenital stationary night blindness
23. Serum Biomarkers and Trafficking Defects in Peripheral Tissues Reflect the Severity of Retinopathy in Three Brothers Affected by Choroideremia
24. THE NATURAL HISTORY OF FULL-FIELD STIMULUS THRESHOLD DECLINE IN CHOROIDEREMIA
25. Choroideremia: Towards a Therapy
26. Choroideremia
27. Reduction of Arachidonate Is Associated With Increase in B-Cell Activation Marker in Infants: A Randomized Trial
28. Eyeing a New Network
29. Lessons learned from research on choroideremia
30. AA and DHA are Decreased in Paediatric AD/HD And Inattention is Ameliorated by Increased Plasma DHA
31. Breaking Bad News in Eye Care
32. Wnt1-Cre mediated deletion of BMP7 suggests a role for neural crest-derived BMP7 in retina development and function
33. Iris Flocculi Investigated for Familial Thoracic Aortic Aneurysms and Dissections
34. Effect of docosahexaenoic acid supplementation on the macular function of patients with Best vitelliform macular dystrophy: randomized clinical trial
35. Corneal involvement in a case of autosomal dominant Stargardt-like macular dystrophy (STGD3) with ELOVL4 mutation
36. PEX6 Mutations in Peroxisomal Biogenesis Disorders
37. Validating Ellipsoid Zone Area Measurement With Multimodal Imaging in Choroideremia
38. A retrospective cohort study of radial optic neurotomy for severe central retinal vein occlusions
39. The Need for Standardization of Antiretinal Antibody Detection and Measurement
40. A mutation in SLC24A1 implicated in autosomal-recessive congenital stationary night blindness
41. A homozygous POC1B variant causes recessive cone-rod dystrophy
42. Choroideremia carriers maintain a normal electro-oculogram (EOG)
43. Upward saccadic intrusions as the presenting feature for incomplete congenital stationary night blindness.
44. Preventing blindness in retinal disease: ciliary neurotrophic factor intraocular implants
45. Zebrafish Models of Photoreceptor Dysfunction and Degeneration
46. RP1L1 and inherited photoreceptor disease: A review
47. Choroideremia
48. An internet-based health survey on the co-morbidities of choroideremia patients
49. Serum Biomarkers and Trafficking Defects in Peripheral Tissues Reflect the Severity of Retinopathy in Three Brothers Affected by Choroideremia
50. Mutations in RLBP1 associated with fundus albipunctatus in consanguineous Pakistani families
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.