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Mutations in WDR4 as a new cause of Galloway-Mowat syndrome.
Braun DA, Shril S, Sinha A, Schneider R, Tan W, Ashraf S, Hermle T, Jobst-Schwan T, Widmeier E, Majmundar AJ, Daga A, Warejko JK, Nakayama M, Schapiro D, Chen J, Airik M, Rao J, Schmidt JM, Hoogstraten CA, Hugo H, Meena J, Lek M, Laricchia KM, Bagga A, Hildebrandt F. Braun DA, et al. Among authors: bagga a. Am J Med Genet A. 2018 Nov;176(11):2460-2465. doi: 10.1002/ajmg.a.40489. Epub 2018 Aug 6. Am J Med Genet A. 2018. PMID: 30079490 Free PMC article.
Patients with mutations in NPHS2 (podocin) do not respond to standard steroid treatment of nephrotic syndrome.
Ruf RG, Lichtenberger A, Karle SM, Haas JP, Anacleto FE, Schultheiss M, Zalewski I, Imm A, Ruf EM, Mucha B, Bagga A, Neuhaus T, Fuchshuber A, Bakkaloglu A, Hildebrandt F; Arbeitsgemeinschaft Für Pädiatrische Nephrologie Study Group. Ruf RG, et al. Among authors: bagga a. J Am Soc Nephrol. 2004 Mar;15(3):722-32. doi: 10.1097/01.asn.0000113552.59155.72. J Am Soc Nephrol. 2004. PMID: 14978175
Evaluation of renal tubular acidosis.
Bagga A, Sinha A. Bagga A, et al. Indian J Pediatr. 2007 Jul;74(7):679-86. doi: 10.1007/s12098-007-0120-0. Indian J Pediatr. 2007. PMID: 17699978 Review.
Pulse steroid therapy.
Sinha A, Bagga A. Sinha A, et al. Among authors: bagga a. Indian J Pediatr. 2008 Oct;75(10):1057-66. doi: 10.1007/s12098-008-0210-7. Epub 2008 Nov 21. Indian J Pediatr. 2008. PMID: 19023530
Gitelman syndrome: novel mutation and long-term follow-up.
Sinha A, Lněnička P, Basu B, Gulati A, Hari P, Bagga A. Sinha A, et al. Among authors: bagga a. Clin Exp Nephrol. 2012 Apr;16(2):306-9. doi: 10.1007/s10157-011-0542-x. Epub 2011 Oct 4. Clin Exp Nephrol. 2012. PMID: 21964762
408 results