Ramprasad VL - Search Results

1

Biosynthetic and functional defects in newly identified SLC4A11 mutants and absence of COL8A2 mutations in Fuchs endothelial corneal dystrophy.

Soumittra N, Loganathan SK, Madhavan D, Ramprasad VL, Arokiasamy T, Sumathi S, Karthiyayini T, Rachapalli SR, Kumaramanickavel G, Casey JR, Rajagopal R. Soumittra N, et al. Among authors: ramprasad vl. J Hum Genet. 2014 Aug;59(8):444-53. doi: 10.1038/jhg.2014.55. Epub 2014 Jul 10. J Hum Genet. 2014. PMID: 25007886

2

Inducible nitric oxide synthase gene and diabetic retinopathy in Asian Indian patients.

Kumaramanickavel G, Sripriya S, Vellanki RN, Upadyay NK, Badrinath SS, Rajendran V, Sukumar B, Ramprasad VL, Sharma T. Kumaramanickavel G, et al. Among authors: ramprasad vl. Clin Genet. 2002 May;61(5):344-8. doi: 10.1046/j.0009-9163.2002.00251.x. Clin Genet. 2002. PMID: 12081717

3

Association of Gly82Ser polymorphism in the RAGE gene with diabetic retinopathy in type II diabetic Asian Indian patients.

Kumaramanickavel G, Ramprasad VL, Sripriya S, Upadyay NK, Paul PG, Sharma T. Kumaramanickavel G, et al. Among authors: ramprasad vl. J Diabetes Complications. 2002 Nov-Dec;16(6):391-4. doi: 10.1016/s1056-8727(02)00187-3. J Diabetes Complications. 2002. PMID: 12477623

4

Z-2 aldose reductase allele and diabetic retinopathy in India.

Kumaramanickavel G, Sripriya S, Ramprasad VL, Upadyay NK, Paul PG, Sharma T. Kumaramanickavel G, et al. Among authors: ramprasad vl. Ophthalmic Genet. 2003 Mar;24(1):41-8. doi: 10.1076/opge.24.1.41.13889. Ophthalmic Genet. 2003. PMID: 12660865

5

Truncating mutation in the NHS gene: phenotypic heterogeneity of Nance-Horan syndrome in an asian Indian family.

Ramprasad VL, Thool A, Murugan S, Nancarrow D, Vyas P, Rao SK, Vidhya A, Ravishankar K, Kumaramanickavel G. Ramprasad VL, et al. Invest Ophthalmol Vis Sci. 2005 Jan;46(1):17-23. doi: 10.1167/iovs.04-0477. Invest Ophthalmol Vis Sci. 2005. PMID: 15623749

6

Genetic homogeneity for inherited congenital microcoria loci in an Asian Indian pedigree.

Ramprasad VL, Sripriya S, Ronnie G, Nancarrow D, Saxena S, Hemamalini A, Kumar D, Vijaya L, Kumaramanickavel G. Ramprasad VL, et al. Mol Vis. 2005 Nov 3;11:934-40. Mol Vis. 2005. PMID: 16288197 Free article.

7

Retinoblastoma: a diagnostic model for India.

Joseph B, Madhavan J, Mamatha G, Ramprasad VL, Gopal L, Kumaramanickavel G. Joseph B, et al. Among authors: ramprasad vl. Asian Pac J Cancer Prev. 2006 Jul-Sep;7(3):485-8. Asian Pac J Cancer Prev. 2006. PMID: 17059352 Free article.

8

Retinoblastoma in India : microsatellite analysis and its application in genetic counseling.

Ramprasad VL, Madhavan J, Murugan S, Sujatha J, Suresh S, Sharma T, Kumaramanickavel G. Ramprasad VL, et al. Mol Diagn Ther. 2007;11(1):63-70. doi: 10.1007/BF03256223. Mol Diagn Ther. 2007. PMID: 17286451

9

Novel SLC4A11 mutations in patients with recessive congenital hereditary endothelial dystrophy (CHED2). Mutation in brief #958. Online.

Ramprasad VL, Ebenezer ND, Aung T, Rajagopal R, Yong VH, Tuft SJ, Viswanathan D, El-Ashry MF, Liskova P, Tan DT, Bhattacharya SS, Kumaramanickavel G, Vithana EN. Ramprasad VL, et al. Hum Mutat. 2007 May;28(5):522-3. doi: 10.1002/humu.9487. Hum Mutat. 2007. PMID: 17397048

10

Molecular genetic analysis of a consanguineous south Indian family with congenital glaucoma: relevance of genetic testing and counseling.

Ramprasad VL, George RJ, Sripriya S, Nirmaladevi J, Vijaya L, Kumaramanickavel G. Ramprasad VL, et al. Ophthalmic Genet. 2007 Mar;28(1):17-24. doi: 10.1080/13816810701199449. Ophthalmic Genet. 2007. PMID: 17454743

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