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A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome.
Sadowski CE, Lovric S, Ashraf S, Pabst WL, Gee HY, Kohl S, Engelmann S, Vega-Warner V, Fang H, Halbritter J, Somers MJ, Tan W, Shril S, Fessi I, Lifton RP, Bockenhauer D, El-Desoky S, Kari JA, Zenker M, Kemper MJ, Mueller D, Fathy HM, Soliman NA; SRNS Study Group; Hildebrandt F. Sadowski CE, et al. J Am Soc Nephrol. 2015 Jun;26(6):1279-89. doi: 10.1681/ASN.2014050489. Epub 2014 Oct 27. J Am Soc Nephrol. 2015. PMID: 25349199 Free PMC article.
Diagnostic Code-Based Screening for Identifying Children with Primary Hyperoxaluria.
Tasian G, Dickinson K, Karafilidis J, Marchesani N, Antunes N, Razzaghi H, Utidjian L, Yonekawa K, Coplen D, Muneeruddin S, DeFoor B, Rove KO, Forrest C, Ching C. Tasian G, et al. Among authors: muneeruddin s. J Urol. 2022 Oct;208(4):898-905. doi: 10.1097/JU.0000000000002863. Epub 2022 Aug 5. J Urol. 2022. PMID: 35930731 Review.
Isosorbide dinitrate in nephronophthisis treatment.
Strong A, Muneeruddin S, Parrish R, Lui D, Conley SB. Strong A, et al. Among authors: muneeruddin s. Am J Med Genet A. 2018 Apr;176(4):1023-1026. doi: 10.1002/ajmg.a.38650. Am J Med Genet A. 2018. PMID: 29575630
The real world experience of pediatric primary hyperoxaluria patients in the PEDSnet clinical research network.
Ching CB, Dickinson K, Karafilidis J, Marchesani N, Mucha L, Antunes N, Razzaghi H, Utidjian L, Yonekawa K, Coplen DE, Muneeruddin S, DeFoor W, Rove KO, Forrest CB, Tasian GE. Ching CB, et al. Among authors: muneeruddin s. Eur J Pediatr. 2023 Sep;182(9):4027-4036. doi: 10.1007/s00431-023-05077-y. Epub 2023 Jul 1. Eur J Pediatr. 2023. PMID: 37392234
Two decades of pediatric kidney transplantation in a multi-ethnic cohort.
Muneeruddin S, Chandar J, Abitbol CL, Seeherunvong W, Freundlich M, Ciancio G, Burke GW, Zilleruelo G. Muneeruddin S, et al. Pediatr Transplant. 2010 Aug;14(5):667-74. doi: 10.1111/j.1399-3046.2010.01323.x. Epub 2010 May 31. Pediatr Transplant. 2010. PMID: 20534024