1. ScholarBank@NUS

Eranga Nishanthie Vithana

rp04332

Collaboration Map View Statistics Email Alert RSS Feed

Profile

Full Name
Eranga Nishanthie Vithana
Variants
Vithana E.N
Vithana, E.N.
Vithana, Eranga Nishanthie
 
Main Affiliation
 
Faculty
 
Email
ophenv@nus.edu.sg
 

Publications

Refined By:
Author:  Tan, D.T.H.

Results 1-7 of 7 (Search time: 0.005 seconds).

Issue DateTitleAuthor(s)
12010Absence of phenotype-genotype correlation of patients expressing mutations in the SLC4A11 geneMehta, J.S.; Tan, D.T. ; Aung, T. ; Vithana, E.N. ; Hemadevi, B.; Sundaresan, P.; Arunkumar, J.; Srinivasan, M.; Prajna, V.
22008Analysis of conjunctival fibroblasts from a proband with Schnyder corneal dystrophyMehta, J.S.; Vithana, E.N. ; Venkataraman, D.; Venkatraman, A.; Poh, R.; Beuerman, R.W. ; Aung, T. ; Tan, D.T.H. 
32008Analysis of the posterior polymorphous corneal dystrophy 3 gene, TCF8, in late-onset fuchs endothelial corneal dystrophyMehta, J.S.; Vithana, E.N. ; Tan, D.T.H. ; Yong, V.H.K.; Aung, T. ; Yam, G.H.F.; Law, R.W.K.; Pang, C.P.
42006Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)Vithana, E.N. ; Tan, D.T.H. ; Venkataraman, D.; Yong, V.H.K.; Aung, T. ; Morgan, P.; Casey, J.R.; Sundaresan, P.; Hemadevi, B.; Srinivasan, M.; Prajna, V.; Ebenezer, N.D.; Mohamed, M.D.; Inglehearn, C.F.; Anand, S.; Khine, K.O.; Salto-Tellez, M. ; Guo, K.
52006Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)Vithana, E.N. ; Tan, D.T.H. ; Yong, V.H.K.; Morgan, P.; Casey, J.R.; Sundaresan, P.; Hemadevi, B.; Srinivasan, M.; Prajna, V.; Ebenezer, N.D.; Mohamed, M.D.; Inglehearn, C.F.; Anand, S.; Khine, K.O.; Khine, M.; Salto-Tellez, M. ; Guo, K.
62008SLC4A11 mutations in Fuchs endothelial corneal dystrophyVithana, E.N. ; Tan, D.T.H. ; Venkataraman, D.; Venkatraman, A.; Aung, T. ; Morgan, P.E.; Casey, J.R.; Ramprasad, V.; Nagasamy, S.; Kumaramanickevel, G.; Rajagopal, R.; Yam, G.H.F.; Law, R.W.K.; Pang, C.P.; Yong, V.H.K
72009Surgical management and genetic analysis of a Chinese family with the S171P mutation in the UBIAD1 gene, the gene for Schnyder corneal dystrophyMehta, J.S.; Vithana, E.N. ; Venkataraman, D.; Venkatraman, A.; Yong, V.H.K.; Aung, T. ; Tan, D.T.H.