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Tubulointerstitial nephritis and Fanconi syndrome in primary biliary cirrhosis.
Lino M, Binaut R, Noël LH, Patey N, Rustin P, Daniel L, Serpaggi J, Varaut A, Vanhille P, Knebelmann B, Grünfeld JP, Fakhouri F. Lino M, et al. Among authors: knebelmann b. Am J Kidney Dis. 2005 Sep;46(3):e41-6. doi: 10.1053/j.ajkd.2005.05.021. Am J Kidney Dis. 2005. PMID: 16129198 Review.
Deletions in the COL4A5 collagen gene in X-linked Alport syndrome. Characterization of the pathological transcripts in nonrenal cells and correlation with disease expression.
Antignac C, Knebelmann B, Drouot L, Gros F, Deschênes G, Hors-Cayla MC, Zhou J, Tryggvason K, Grünfeld JP, Broyer M, et al. Antignac C, et al. Among authors: knebelmann b. J Clin Invest. 1994 Mar;93(3):1195-207. doi: 10.1172/JCI117073. J Clin Invest. 1994. PMID: 8132760 Free PMC article.
A molecular approach to inherited kidney disorders.
Knebelmann B, Antignac C, Gubler NC, Grünfeld JP. Knebelmann B, et al. Kidney Int. 1993 Dec;44(6):1205-16. doi: 10.1038/ki.1993.370. Kidney Int. 1993. PMID: 8301921 Free article. Review. No abstract available.
Genetic, clinical, and morphologic heterogeneity in Alport's syndrome.
Gubler MC, Antignac C, Deschênes G, Knebelmann B, Hors-Cayla MC, Grünfeld JP, Broyer M, Habib R. Gubler MC, et al. Among authors: knebelmann b. Adv Nephrol Necker Hosp. 1993;22:15-35. Adv Nephrol Necker Hosp. 1993. PMID: 8427057 Review. No abstract available.
161 results