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Page 1
Ciliary function of polycystins: a new model for cystogenesis.
Joly D, Hummel A, Ruello A, Knebelmann B. Joly D, et al. Among authors: knebelmann b. Nephrol Dial Transplant. 2003 Sep;18(9):1689-92. doi: 10.1093/ndt/gfg256. Nephrol Dial Transplant. 2003. PMID: 12937209 No abstract available.
Reversible paraparesis in multiple myeloma with renal failure.
Terrier B, Joly D, Ghez D, Knebelmann B, Fakhouri F, Hummel A. Terrier B, et al. Among authors: knebelmann b. Nephrol Dial Transplant. 2006 May;21(5):1439-40. doi: 10.1093/ndt/gfl086. Epub 2006 Mar 6. Nephrol Dial Transplant. 2006. PMID: 16520348 No abstract available.
Post-allogeneic haematopoietic stem cell transplantation membranous nephropathy: clinical presentation, outcome and pathogenic aspects.
Terrier B, Delmas Y, Hummel A, Presne C, Glowacki F, Knebelmann B, Combe C, Lesavre P, Maillard N, Noël LH, Patey-Mariaud de Serre N, Nusbaum S, Radford I, Buzyn A, Fakhouri F. Terrier B, et al. Among authors: knebelmann b. Nephrol Dial Transplant. 2007 May;22(5):1369-76. doi: 10.1093/ndt/gfl795. Epub 2007 Jan 25. Nephrol Dial Transplant. 2007. PMID: 17255123
Quiz page: a familial glomerulopathy.
Cez A, Galmiche L, Hummel A, Knebelmann B, El Karoui K. Cez A, et al. Among authors: knebelmann b. Am J Kidney Dis. 2014 Apr;63(4):A17-20. doi: 10.1053/j.ajkd.2013.09.023. Am J Kidney Dis. 2014. PMID: 24670484 No abstract available.
APOL1 risk genotype in European steroid-resistant nephrotic syndrome and/or focal segmental glomerulosclerosis patients of different African ancestries.
Gribouval O, Boyer O, Knebelmann B, Karras A, Dantal J, Fourrage C, Alibeu O, Hogan J, Dossier C, Tête MJ, Antignac C, Servais A. Gribouval O, et al. Among authors: knebelmann b. Nephrol Dial Transplant. 2019 Nov 1;34(11):1885-1893. doi: 10.1093/ndt/gfy176. Nephrol Dial Transplant. 2019. PMID: 29992269
Erythrocytosis associated with IgA nephropathy.
Cohen C, Coulon S, Bhukhai K, Neuraz A, Dussiot M, Fouquet G, Stang ML, Flamant M, Vrtovsnik F, Hummel A, Knebelmann B, Mesnard L, Rondeau E, Maciel TT, Favale F, Casadevall N, Nguyen-Khoa T, Moutereau S, Legendre C, Benhamou M, Monteiro RC, Hermine O, El Karoui K, Moura IC. Cohen C, et al. Among authors: knebelmann b. EBioMedicine. 2022 Jan;75:103785. doi: 10.1016/j.ebiom.2021.103785. Epub 2021 Dec 24. EBioMedicine. 2022. PMID: 34959131 Free PMC article.
The 2019 and 2021 International Workshops on Alport Syndrome.
Daga S, Ding J, Deltas C, Savige J, Lipska-Ziętkiewicz BS, Hoefele J, Flinter F, Gale DP, Aksenova M, Kai H, Perin L, Barua M, Torra R, Miner JH, Massella L, Ljubanović DG, Lennon R, Weinstock AB, Knebelmann B, Cerkauskaite A, Gear S, Gross O, Turner AN, Baldassarri M, Pinto AM, Renieri A. Daga S, et al. Among authors: knebelmann b. Eur J Hum Genet. 2022 May;30(5):507-516. doi: 10.1038/s41431-022-01075-0. Epub 2022 Mar 9. Eur J Hum Genet. 2022. PMID: 35260866 Free PMC article.
169 results