Shukla P - Search Results

1

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. 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

2

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. Prenat Diagn. 2008 Apr;28(4):357-9. doi: 10.1002/pd.1931. Prenat Diagn. 2008. PMID: 18330867 No abstract available.

3

De novo ABCD1 gene mutation in an Indian patient with adrenoleukodystrophy.

Kumar N, Shukla P, Taneja KK, Kalra V, Bansal SK. Kumar N, et al. Among authors: shukla p. Pediatr Neurol. 2008 Oct;39(4):289-92. doi: 10.1016/j.pediatrneurol.2008.07.006. Pediatr Neurol. 2008. PMID: 18805372

4

Megalencephalic leukodystrophy with simple hemihyperplasia: a rare association.

Shukla P, Gupta N, Balakrishnan P, Ghosh M, Gupta AK, Sharma R, Kabra M. Shukla P, et al. Clin Dysmorphol. 2009 Jan;18(1):49-51. doi: 10.1097/MCD.0b013e3283136919. Clin Dysmorphol. 2009. PMID: 19050405 No abstract available.

5

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. J Child Neurol. 2009 Jul;24(7):857-60. doi: 10.1177/0883073808330764. Epub 2009 Apr 30. J Child Neurol. 2009. PMID: 19406751

6

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. Hum Genet. 2009 Aug;126(2):335-6. Hum Genet. 2009. PMID: 19694007 No abstract available.

7

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. Pediatr Neurol. 2011 Jun;44(6):450-8. doi: 10.1016/j.pediatrneurol.2011.01.003. Pediatr Neurol. 2011. PMID: 21555057

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. 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

Cataract surgical coverage in Indian population aged 50 years and above.

Vashist P, Sarath S, Gupta V, Gupta N, Senjam SS, Shukla P, Grover S, Shamanna BR, Vemparala R, Wadhwani M, Bhardwaj A, Titiyal JS. Vashist P, et al. Among authors: shukla p. Indian J Ophthalmol. 2025 Mar 1;73(3):347-351. doi: 10.4103/IJO.IJO_1398_24. Epub 2024 Dec 27. Indian J Ophthalmol. 2025. PMID: 39728729 Free PMC article.

10

Gene symbol: ABCD1. Disease: Adrenoleukodystrophy.

Shukla P. Shukla P. Hum Genet. 2008 Oct;124(3):312. Hum Genet. 2008. PMID: 18846654 No abstract available.

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