Kalra V - Search Results

1

Prenatal diagnosis of megalencephalic leukodystrophy.

Shukla P, Balakrishnan P, Agarwal N, Ghosh M, Kabra M, Sharma R, Deka D, Kalra V. Shukla P, et al. Among authors: kalra v. Prenat Diagn. 2008 Apr;28(4):357-9. doi: 10.1002/pd.1931. Prenat Diagn. 2008. PMID: 18330867 No abstract available.

2

Molecular genetic studies in Indian patients with megalencephalic leukoencephalopathy.

Shukla P, Gupta N, Ghosh M, Vasisht S, Gulati S, Balakrishnan P, Sharma R, Gupta AK, Kamate M, Kalra V, Kabra M. Shukla P, et al. Among authors: kalra v. Pediatr Neurol. 2011 Jun;44(6):450-8. doi: 10.1016/j.pediatrneurol.2011.01.003. Pediatr Neurol. 2011. PMID: 21555057

3

A novel MECP2 change in an indian boy with variant rett phenotype and congenital blindness: implications for genetic counseling and prenatal diagnosis.

Khajuria R, Gupta N, Sapra S, Gulati S, Ghosh M, Kalra V, Kabra M. Khajuria R, et al. Among authors: kalra v. J Child Neurol. 2011 Feb;26(2):209-13. doi: 10.1177/0883073810378535. J Child Neurol. 2011. PMID: 21285040

4

Molecular and structural analysis of metachromatic leukodystrophy patients in Indian population.

Shukla P, Vasisht S, Srivastava R, Gupta N, Ghosh M, Kumar M, Sharma R, Gupta AK, Kaur P, Kamate M, Gulati S, Kalra V, Phadke S, Singhi P, Dherai AJ, Kabra M. Shukla P, et al. Among authors: kalra v. J Neurol Sci. 2011 Feb 15;301(1-2):38-45. doi: 10.1016/j.jns.2010.11.007. Epub 2010 Dec 16. J Neurol Sci. 2011. PMID: 21167507

5

Novel human pathological mutations. Gene symbol: ABCD1. Disease: Adrenoleukodystrophy.

Shukla P, Gupta N, Kabra M, Ghosh M, Gulati S, Kalra V. Shukla P, et al. Among authors: kalra v. Hum Genet. 2009 Aug;126(2):335-6. Hum Genet. 2009. PMID: 19694007 No abstract available.

6

Novel non-identical MECP2 mutations in Rett syndrome family: a rare presentation.

Khajuria R, Gupta N, Sapra S, Gulati S, Ghosh M, Kalra V, Kabra M. Khajuria R, et al. Among authors: kalra v. Brain Dev. 2012 Jan;34(1):28-31. doi: 10.1016/j.braindev.2011.01.006. Epub 2011 Feb 5. Brain Dev. 2012. PMID: 21300488

7

Three novel variants in X-linked adrenoleukodystrophy.

Shukla P, Gupta N, Kabra M, Ghosh M, Sharma R, Gupta AK, Gulati S, Kalra V. Shukla P, et al. Among authors: kalra v. J Child Neurol. 2009 Jul;24(7):857-60. doi: 10.1177/0883073808330764. Epub 2009 Apr 30. J Child Neurol. 2009. PMID: 19406751

8

Molecular analysis of ABCD1 gene in Indian patients with X-linked adrenoleukodystrophy.

Shukla P, Gupta N, Gulati S, Ghosh M, Vasisht S, Sharma R, Gupta AK, Kalra V, Kabra M. Shukla P, et al. Among authors: kalra v. Clin Chim Acta. 2011 Nov 20;412(23-24):2289-95. doi: 10.1016/j.cca.2011.08.026. Epub 2011 Aug 26. Clin Chim Acta. 2011. PMID: 21889498

9

Rapid detection of deletions in hotspot C-terminal segment region of MECP2 by routine PCR method: report of two classical Rett syndrome patients of Indian origin.

Khajuria R, Sapra S, Ghosh M, Gupta N, Gulati S, Kalra V, Kabra M. Khajuria R, et al. Among authors: kalra v. Genet Test Mol Biomarkers. 2009 Apr;13(2):277-80. doi: 10.1089/gtmb.2008.0142. Genet Test Mol Biomarkers. 2009. PMID: 19371229

10

Novel human pathological mutations. Gene symbol: MECP2. Disease: Rett Syndrome.

Khajuria R, Sapra S, Ghosh M, Gupta N, Gulati S, Kalra V, Kabra M. Khajuria R, et al. Among authors: kalra v. Hum Genet. 2010 Jan;127(1):117. Hum Genet. 2010. PMID: 20108429 No abstract available.

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