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Clinical trial recommendations for potential Alport syndrome therapies.
Weinstock BA, Feldman DL, Fornoni A, Gross O, Kashtan CE, Lagas S, Lennon R, Miner JH, Rheault MN, Simon JF; Workshop Participants. Weinstock BA, et al. Kidney Int. 2020 Jun;97(6):1109-1116. doi: 10.1016/j.kint.2020.02.029. Epub 2020 Apr 6. Kidney Int. 2020. PMID: 32386680 Free PMC article.
The STAGED-PKD 2-Stage Adaptive Study With a Patient Enrichment Strategy and Treatment Effect Modeling for Improved Study Design Efficiency in Patients With ADPKD.
Perrone RD, Hariri A, Minini P, Ahn C, Chapman AB, Horie S, Knebelmann B, Mrug M, Ong ACM, Pei YPC, Torres VE, Modur V, Gansevoort RT. Perrone RD, et al. Among authors: hariri a. Kidney Med. 2022 Aug 27;4(10):100538. doi: 10.1016/j.xkme.2022.100538. eCollection 2022 Oct. Kidney Med. 2022. PMID: 36204243 Free PMC article.
Drug Development in Kidney Disease: Proceedings From a Multistakeholder Conference.
Edmonston DL, Roe MT, Block G, Conway PT, Dember LM, DiBattiste PM, Greene T, Hariri A, Inker LA, Isakova T, Montez-Rath ME, Nkulikiyinka R, Polidori D, Roessig L, Tangri N, Wyatt C, Chertow GM, Wolf M. Edmonston DL, et al. Among authors: hariri a. Am J Kidney Dis. 2020 Dec;76(6):842-850. doi: 10.1053/j.ajkd.2020.05.026. Epub 2020 Aug 5. Am J Kidney Dis. 2020. PMID: 32768631 Review.
Mitochondrial DNA mutations in renal disease: an overview.
Govers LP, Toka HR, Hariri A, Walsh SB, Bockenhauer D. Govers LP, et al. Among authors: hariri a. Pediatr Nephrol. 2021 Jan;36(1):9-17. doi: 10.1007/s00467-019-04404-6. Epub 2020 Jan 10. Pediatr Nephrol. 2021. PMID: 31925537 Free PMC article. Review.
The molecular basis of blood pressure variation.
Toka HR, Koshy JM, Hariri A. Toka HR, et al. Among authors: hariri a. Pediatr Nephrol. 2013 Mar;28(3):387-99. doi: 10.1007/s00467-012-2206-9. Epub 2012 Jul 5. Pediatr Nephrol. 2013. PMID: 22763847 Review.
Congenital anomalies of kidney and urinary tract.
Toka HR, Toka O, Hariri A, Nguyen HT. Toka HR, et al. Among authors: hariri a. Semin Nephrol. 2010 Jul;30(4):374-86. doi: 10.1016/j.semnephrol.2010.06.004. Semin Nephrol. 2010. PMID: 20807610
A cluster of metabolic defects caused by mutation in a mitochondrial tRNA.
Wilson FH, Hariri A, Farhi A, Zhao H, Petersen KF, Toka HR, Nelson-Williams C, Raja KM, Kashgarian M, Shulman GI, Scheinman SJ, Lifton RP. Wilson FH, et al. Among authors: hariri a. Science. 2004 Nov 12;306(5699):1190-4. doi: 10.1126/science.1102521. Epub 2004 Oct 21. Science. 2004. PMID: 15498972 Free PMC article.
503 results