Kannabiran C - Search Results

1

Updates on congenital hereditary endothelial dystrophy.

Mehta N, Verma A, Achanta DS, Kannabiran C, Roy S, Mishra DK, Chaurasia S, Edward DP, Ramappa M. Mehta N, et al. Among authors: kannabiran c. Taiwan J Ophthalmol. 2023 Nov 28;13(4):405-416. doi: 10.4103/tjo.TJO-D-23-00135. eCollection 2023 Oct-Dec. Taiwan J Ophthalmol. 2023. PMID: 38249503 Free PMC article. Review.

2

Bilateral granular dystrophy: A clinicopathogenetic correlation after alcohol assisted debridement with phototherapeutic keratectomy.

Sati A, Ramappa M, Sharma N, Chaurasia S, Vemuganti GK, Kannabiran C, Garg P. Sati A, et al. Among authors: kannabiran c. Med J Armed Forces India. 2015 Jul;71(Suppl 1):S1-4. doi: 10.1016/j.mjafi.2012.08.023. Epub 2012 Nov 29. Med J Armed Forces India. 2015. PMID: 26265796 Free PMC article. No abstract available.

3

Parents of Patients With Congenital Hereditary Endothelial Dystrophy Should Be Evaluated for Fuchs Endothelial Corneal Dystrophy.

Chaurasia S, Ramappa M, Kannabiran C. Chaurasia S, et al. Among authors: kannabiran c. Cornea. 2017 Dec;36(12):e34-e35. doi: 10.1097/ICO.0000000000001397. Cornea. 2017. PMID: 28976417 No abstract available.

4

Coexistence of Congenital Hereditary Endothelial Dystrophy and Fuchs Endothelial Corneal Dystrophy Associated With SLC4A11 Mutations in Affected Families.

Chaurasia S, Ramappa M, Annapurna M, Kannabiran C. Chaurasia S, et al. Among authors: kannabiran c. Cornea. 2020 Mar;39(3):354-357. doi: 10.1097/ICO.0000000000002183. Cornea. 2020. PMID: 31714402

5

Macular Corneal Dystrophy: An Updated Review.

Singh S, Das S, Kannabiran C, Jakati S, Chaurasia S. Singh S, et al. Among authors: kannabiran c. Curr Eye Res. 2021 Jun;46(6):765-770. doi: 10.1080/02713683.2020.1849727. Epub 2020 Nov 29. Curr Eye Res. 2021. PMID: 33171054 Review.

6

Update on the genetics of corneal endothelial dystrophies.

Kannabiran C, Chaurasia S, Ramappa M, Mootha VV. Kannabiran C, et al. Indian J Ophthalmol. 2022 Jul;70(7):2239-2248. doi: 10.4103/ijo.IJO_992_22. Indian J Ophthalmol. 2022. PMID: 35791103 Free PMC article. Review.

7

Identification and in silico analysis of a spectrum of SLC4A11 variations in Indian familial and sporadic cases of congenital hereditary endothelial dystrophy.

Salman M, Verma A, Chaurasia S, Prasad D, Kannabiran C, Singh V, Ramappa M. Salman M, et al. Among authors: kannabiran c. Orphanet J Rare Dis. 2022 Sep 17;17(1):361. doi: 10.1186/s13023-022-02521-4. Orphanet J Rare Dis. 2022. PMID: 36115991 Free PMC article.

8

Correction to: identification and in silico analysis of a spectrum of SLC4A11 variations in indian familial and sporadic cases of congenital hereditary endothelial dystrophy.

Salman M, Verma A, Chaurasia S, Prasad D, Kannabiran C, Singh V, Ramappa M. Salman M, et al. Among authors: kannabiran c. Orphanet J Rare Dis. 2023 Jun 29;18(1):170. doi: 10.1186/s13023-023-02791-6. Orphanet J Rare Dis. 2023. PMID: 37386499 Free PMC article. No abstract available.

9

Genotype-phenotype correlation in 2 Indian families with severe granular corneal dystrophy.

Kannabiran C, Sridhar MS, Chakravarthi SK, Vemuganti GK, Lakshmipathi M. Kannabiran C, et al. Arch Ophthalmol. 2005 Aug;123(8):1127-33. doi: 10.1001/archopht.123.8.1127. Arch Ophthalmol. 2005. PMID: 16087849

10

Mutational spectrum of the SLC4A11 gene in autosomal recessive congenital hereditary endothelial dystrophy.

Sultana A, Garg P, Ramamurthy B, Vemuganti GK, Kannabiran C. Sultana A, et al. Among authors: kannabiran c. Mol Vis. 2007 Jul 26;13:1327-32. Mol Vis. 2007. PMID: 17679935

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

68 results

Search Page