Khandelwal P - Search Results

1

Variants in complement genes are uncommon in patients with anti-factor H autoantibody-associated atypical hemolytic uremic syndrome.

Khandelwal P, Joshi A, Mathur A, Puraswani M, Gurjar BS, Sinha A, Hari P, Faruq M, Bagga A. Khandelwal P, et al. Pediatr Nephrol. 2023 Aug;38(8):2659-2668. doi: 10.1007/s00467-022-05862-1. Epub 2023 Jan 9. Pediatr Nephrol. 2023. PMID: 36622444

2

Outcomes of renal transplant in patients with anti-complement factor H antibody-associated hemolytic uremic syndrome.

Khandelwal P, Sinha A, Hari P, Bansal VK, Dinda AK, Bagga A. Khandelwal P, et al. Pediatr Transplant. 2014 Aug;18(5):E134-9. doi: 10.1111/petr.12273. Epub 2014 May 12. Pediatr Transplant. 2014. PMID: 24814615

3

Effect of plasma exchange and immunosuppressive medications on antibody titers and outcome in anti-complement factor H antibody-associated hemolytic uremic syndrome.

Khandelwal P, Gupta A, Sinha A, Saini S, Hari P, Dragon Durey MA, Bagga A. Khandelwal P, et al. Pediatr Nephrol. 2015 Mar;30(3):451-7. doi: 10.1007/s00467-014-2948-7. Epub 2014 Sep 13. Pediatr Nephrol. 2015. PMID: 25217328

4

Plasma exchanges and immunosuppression for anti-complement factor H associated hemolytic uremic syndrome.

Khandelwal P, Sinha A, Hari P, Bagga A. Khandelwal P, et al. Indian Pediatr. 2014 Oct;51(10):833-5. Indian Pediatr. 2014. PMID: 25362019 Free article.

5

Experience with Continuous Renal Replacement Therapy.

Khandelwal P, Sharma S, Bhardwaj S, Thergaonkar RW, Sinha A, Hari P, Lodha R, Bagga A. Khandelwal P, et al. Indian J Pediatr. 2015 Aug;82(8):752-4. doi: 10.1007/s12098-015-1743-1. Epub 2015 Mar 18. Indian J Pediatr. 2015. PMID: 25776002

6

Incomplete penetrance of CD46 mutation causing familial atypical hemolytic uremic syndrome.

Bhatia D, Khandelwal P, Sinha A, Hari P, Cheong HI, Bagga A. Bhatia D, et al. Among authors: khandelwal p. Pediatr Nephrol. 2015 Dec;30(12):2215-20. doi: 10.1007/s00467-015-3189-0. Epub 2015 Aug 26. Pediatr Nephrol. 2015. PMID: 26307634

7

Dyslipidemia, carotid intima-media thickness and endothelial dysfunction in children with chronic kidney disease.

Khandelwal P, Murugan V, Hari S, Lakshmy R, Sinha A, Hari P, Bagga A. Khandelwal P, et al. Pediatr Nephrol. 2016 Aug;31(8):1313-20. doi: 10.1007/s00467-016-3350-4. Epub 2016 Feb 26. Pediatr Nephrol. 2016. PMID: 26921213

8

Fanconi syndrome and neonatal diabetes: phenotypic heterogeneity in patients with GLUT2 defects.

Khandelwal P, Sinha A, Jain V, Houghton J, Hari P, Bagga A. Khandelwal P, et al. CEN Case Rep. 2018 May;7(1):1-4. doi: 10.1007/s13730-017-0278-x. Epub 2017 Nov 8. CEN Case Rep. 2018. PMID: 29116606 Free PMC article.

9

Characterization of genetic predisposition and autoantibody profile in atypical haemolytic-uraemic syndrome.

Gurjar BS, Manikanta Sriharsha T, Bhasym A, Prabhu S, Puraswani M, Khandelwal P, Saini H, Saini S, Verma AK, Chatterjee P, Guchhait P, Bal V, George A, Rath S, Sahu A, Sharma A, Hari P, Sinha A, Bagga A. Gurjar BS, et al. Among authors: khandelwal p. Immunology. 2018 Feb 27;154(4):663-72. doi: 10.1111/imm.12916. Online ahead of print. Immunology. 2018. PMID: 29485195 Free PMC article.

10

Mutations in membrane cofactor protein (CD46) gene in Indian children with hemolytic uremic syndrome.

Khandelwal P, Birla S, Bhatia D, Puraswani M, Saini H, Sinha A, Hari P, Sharma A, Bagga A. Khandelwal P, et al. Clin Kidney J. 2018 Apr;11(2):198-203. doi: 10.1093/ckj/sfx078. Epub 2017 Aug 10. Clin Kidney J. 2018. PMID: 29644059 Free PMC article.

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