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Pediatric Continuous Renal Replacement Therapy (PCRRT) expert committee recommendation on prescribing prolonged intermittent renal replacement therapy (PIRRT) in critically ill children.
Sethi SK, Mittal A, Nair N, Bagga A, Iyenger A, Ali U, Sinha R, Agarwal I, de Sousa Tavares M, Abeyagunawardena A, Hanif M, Shreshtha D, Moorani K, Asim S, Kher V, Alhasan K, Mourani C, Al Riyami M, Bunchman TE, McCulloch M, Raina R. Sethi SK, et al. Among authors: bagga a. Hemodial Int. 2020 Apr;24(2):237-251. doi: 10.1111/hdi.12821. Epub 2020 Feb 18. Hemodial Int. 2020. PMID: 32072767
Evaluation and management of hypertension.
Bagga A, Jain R, Vijayakumar M, Kanitkar M, Ali U. Bagga A, et al. Indian Pediatr. 2007 Feb;44(2):103-21. Indian Pediatr. 2007. PMID: 17351301 Free article. No abstract available.
Management of steroid sensitive nephrotic syndrome: revised guidelines.
Indian Pediatric Nephrology Group, Indian Academy of Pediatrics; Bagga A, Ali U, Banerjee S, Kanitkar M, Phadke KD, Senguttuvan P, Sethi S, Shah M. Indian Pediatric Nephrology Group, Indian Academy of Pediatrics, et al. Among authors: bagga a. Indian Pediatr. 2008 Mar;45(3):203-14. Indian Pediatr. 2008. PMID: 18367765 Free article. Review.
Mutations in OCRL1 gene in Indian children with Lowe syndrome.
Sethi SK, Bagga A, Gulati A, Hari P, Gupta N, Lunardi J. Sethi SK, et al. Among authors: bagga a. Clin Exp Nephrol. 2008 Oct;12(5):358-362. doi: 10.1007/s10157-008-0059-0. Epub 2008 May 24. Clin Exp Nephrol. 2008. PMID: 18500547
Primary hyperoxaluria type 1 with a novel mutation.
Sethi SK, Waterham HR, Sharma S, Sharma A, Hari P, Bagga A. Sethi SK, et al. Among authors: bagga a. Indian J Pediatr. 2009 Feb;76(2):215-7. doi: 10.1007/s12098-008-0187-2. Epub 2008 Sep 22. Indian J Pediatr. 2009. PMID: 18810341
Vitamin A responsive night blindness in Dent's disease.
Sethi SK, Ludwig M, Kabra M, Hari P, Bagga A. Sethi SK, et al. Among authors: bagga a. Pediatr Nephrol. 2009 Sep;24(9):1765-70. doi: 10.1007/s00467-009-1198-6. Epub 2009 May 15. Pediatr Nephrol. 2009. PMID: 19444483
Hemolytic uremic syndrome due to homozygous factor H deficiency.
Sethi SK, Marie-Agnes DD, Thaker N, Hari P, Bagga A. Sethi SK, et al. Among authors: bagga a. Clin Exp Nephrol. 2009 Oct;13(5):526-530. doi: 10.1007/s10157-009-0205-3. Epub 2009 Jul 1. Clin Exp Nephrol. 2009. PMID: 19568827
405 results