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Page 1
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.
Rapidly progressive glomerulonephritis in children.
Moorani KN, Aziz M, Amanullah F. Moorani KN, et al. Pak J Med Sci. 2022 Jan;38(2):417-425. doi: 10.12669/pjms.38.ICON-2022.5774. Pak J Med Sci. 2022. PMID: 35310798 Free PMC article. Review.
Infantile Spasms: Clinical profile and treatment outcomes.
Kulsoom S, Ibrahim SH, Jafri SK, Moorani KN, Anjum M. Kulsoom S, et al. Among authors: moorani kn. Pak J Med Sci. 2018 Nov-Dec;34(6):1424-1428. doi: 10.12669/pjms.346.15869. Pak J Med Sci. 2018. PMID: 30559797 Free PMC article.
Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicity.
Braun DA, Schueler M, Halbritter J, Gee HY, Porath JD, Lawson JA, Airik R, Shril S, Allen SJ, Stein D, Al Kindy A, Beck BB, Cengiz N, Moorani KN, Ozaltin F, Hashmi S, Sayer JA, Bockenhauer D, Soliman NA, Otto EA, Lifton RP, Hildebrandt F. Braun DA, et al. Among authors: moorani kn. Kidney Int. 2016 Feb;89(2):468-475. doi: 10.1038/ki.2015.317. Kidney Int. 2016. PMID: 26489029 Free PMC article.
20 results