304 results on '"Ramappa, Muralidhar"'
Search Results
2. Clinical and Optical Coherence Tomography Correlation of Recurrence Patterns After Femtosecond Laser–Assisted Anterior Lamellar Keratoplasty in Reis–Bucklers Corneal Dystrophy
3. Correction to: identification and in silico analysis of a spectrum of SLC4A11 variations in indian familial and sporadic cases of congenital hereditary endothelial dystrophy
4. Clinical profile of keratitis treated within 3 months of acute COVID-19 illness at a tertiary care eye centre
5. Clinical and Optical Coherence Tomography Correlation of Recurrence Patterns After Femtosecond Laser–Assisted Anterior Lamellar Keratoplasty in Reis–Bucklers Corneal Dystrophy
6. Characteristics of Corneal Endothelium in Axenfeld Rieger Spectrum
7. New Frontier in the Management of Corneal Dystrophies: Basics, Development, and Challenges in Corneal Gene Therapy and Gene Editing
8. Corneal opacity due to infantile capillary hemangioma: A rare presentation
9. Grand Challenges in global eye health: a global prioritisation process using Delphi method
10. Outcomes of Ahmed Glaucoma Valve Implantation in Eyes with Pediatric Keratoplasty
11. Identification and in silico analysis of a spectrum of SLC4A11 variations in Indian familial and sporadic cases of congenital hereditary endothelial dystrophy
12. Clinical and demographic profile of herpes zoster ophthalmicus: A hospital-based study of 1752 Indian patients.
13. Band-shaped keratopathy in HNF4A-related Fanconi syndrome: a case report and review of the literature.
14. Ectopia Lentis: Clinical profiles in a large cohort of children from a Tertiary Eye Care network in India.
15. Peters Anomaly in Nail-Patella Syndrome: A Case Report and Clinico-Genetic Correlation
16. Updates on congenital hereditary endothelial dystrophy
17. Band-shaped keratopathy in HNF4A -related Fanconi syndrome: a case report and review of the literature
18. Objectively measuring anterior segment alterations in the eyes of mucopolysaccharidoses: Its utility in early diagnosis of glaucoma
19. Clinical diversity in macular corneal dystrophy: an optical coherence tomography study
20. Neurotization of the human cornea - A comprehensive review and an interim report
21. Coexistence of Congenital Hereditary Endothelial Dystrophy and Fuchs Endothelial Corneal Dystrophy Associated With SLC4A11 Mutations in Affected Families
22. Secondary developmental glaucoma in eyes with congenital aphakia
23. Toric intraocular lenses: Expanding indications and preoperative and surgical considerations to improve outcomes
24. Corneal Endothelial Cell Density in Uveal Coloboma Associated With Microcornea
25. Axenfeld–Rieger syndrome in the pediatric population: A review.
26. Characteristics of Corneal Endothelium in Axenfeld Rieger Spectrum.
27. Advancing therapies for anterior segment developmental anomalies
28. Clinical characterization of posterior polymorphous corneal dystrophy in patients of Indian ethnicity
29. Angiopoietin receptor TEK interacts with CYP1B1 in primary congenital glaucoma
30. Selective Endothelialectomy in Peters Anomaly: A Novel Surgical Technique and Its Clinical Outcomes in Children
31. Characteristics of Corneal Endothelium in Axenfeld Rieger Spectrum
32. Unusual corneal epitheliopathy: An unfamiliar adverse effect of topical retinoids
33. Congenital glaucoma in brittle cornea syndrome type 2 with a novel mutation in PRDM5
34. Quantitative corneal neural imaging using in vivo confocal microscopy in cases of congenital corneal anesthesia: A prospective analysis and clinical correlation
35. Commentary: A perspective on pediatric keratoconus: One size does not fit all
36. Unusual 'fish bone pattern' epitheliopathy
37. Bilateral retinal detachment in Goldenhar syndrome
38. Acute endophthalmitis after penetrating and endothelial keratoplasty at a tertiary eye care center over a 13-year period
39. Anterior segment alterations in congenital primary aphakia--a clinicopathologic report of five cases
40. Parents of Patients With Congenital Hereditary Endothelial Dystrophy Should Be Evaluated for Fuchs Endothelial Corneal Dystrophy
41. Novel Proposed Algorithm in Congenital Hereditary Endothelial Dystrophy
42. Identifications and in silico analysis of a spectrum of SLC4A11 mutations in Indian familial and non-familial cases of congenital hereditary endothelial dystrophy
43. Role of AS-OCT in Managing Corneal Disorders
44. Rapid Resolution of Large and Non- Resolving Corneal Hydrops using a modified technique of compression sutures
45. Commentary: Genomic testing is a powerful tool in diagnosing and managing anterior segment dysgenesis
46. Neurotization of the human cornea – A comprehensive review and an interim report
47. Objectively measuring anterior segment alterations in the eyes of mucopolysaccharidoses: Its utility in early diagnosis of glaucoma
48. Toric intraocular lenses: Expanding indications and preoperative and surgical considerations to improve outcomes
49. Secondary developmental glaucoma in eyes with congenital aphakia
50. Update on the genetics of corneal endothelial dystrophies
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