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Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2).
Vithana EN, Morgan P, Sundaresan P, Ebenezer ND, Tan DT, Mohamed MD, Anand S, Khine KO, Venkataraman D, Yong VH, Salto-Tellez M, Venkatraman A, Guo K, Hemadevi B, Srinivasan M, Prajna V, Khine M, Casey JR, Inglehearn CF, Aung T. Vithana EN, et al. Among authors: prajna v. Nat Genet. 2006 Jul;38(7):755-7. doi: 10.1038/ng1824. Epub 2006 Jun 11. Nat Genet. 2006. PMID: 16767101
Rhodococcus ruber as a cause of keratitis.
Lalitha P, Srinivasan M, Prajna V. Lalitha P, et al. Among authors: prajna v. Cornea. 2006 Feb;25(2):238-9. doi: 10.1097/01.ico.0000170690.59960.8c. Cornea. 2006. PMID: 16371792
The Asia Cornea Society Infectious Keratitis Study: A Prospective Multicenter Study of Infectious Keratitis in Asia.
Khor WB, Prajna VN, Garg P, Mehta JS, Xie L, Liu Z, Padilla MDB, Joo CK, Inoue Y, Goseyarakwong P, Hu FR, Nishida K, Kinoshita S, Puangsricharern V, Tan AL, Beuerman R, Young A, Sharma N, Haaland B, Mah FS, Tu EY, Stapleton FJ, Abbott RL, Tan DT; ACSIKS Group. Khor WB, et al. Among authors: prajna vn. Am J Ophthalmol. 2018 Nov;195:161-170. doi: 10.1016/j.ajo.2018.07.040. Epub 2018 Aug 9. Am J Ophthalmol. 2018. PMID: 30098351
Measurement Reliability for Keratitis Morphology.
Kriegel MF, Loo J, Farsiu S, Prajna V, Tuohy M, Kim KH, Valicevic AN, Niziol LM, Tan H, Ashfaq HA, Ballouz D, Woodward MA. Kriegel MF, et al. Among authors: prajna v. Cornea. 2020 Dec;39(12):1503-1509. doi: 10.1097/ICO.0000000000002470. Cornea. 2020. PMID: 32833849 Free PMC article.
34 results