Ramprasad VL - Search Results

1

Retinoblastoma genetics screening and clinical management.

Gupta H, Malaichamy S, Mallipatna A, Murugan S, Jeyabalan N, Suresh Babu V, Ghosh A, Ghosh A, Santhosh S, Seshagiri S, Ramprasad VL, Kumaramanickavel G. Gupta H, et al. Among authors: ramprasad vl. BMC Med Genomics. 2021 Jul 22;14(1):188. doi: 10.1186/s12920-021-01034-6. BMC Med Genomics. 2021. PMID: 34294096 Free PMC article.

2

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

3

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

4

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

5

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.

6

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.

7

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

8

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

9

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

10

Association of non-synonymous single nucleotide polymorphisms in the LOXL1 gene with pseudoexfoliation syndrome in India.

Ramprasad VL, George R, Soumittra N, Sharmila F, Vijaya L, Kumaramanickavel G. Ramprasad VL, et al. Mol Vis. 2008 Feb 9;14:318-22. Mol Vis. 2008. PMID: 18334947 Free PMC article.

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

67 results

Search Page