Knebelmann B - Search Results

1

Early angiotensin-converting enzyme inhibition in Alport syndrome delays renal failure and improves life expectancy.

Gross O, Licht C, Anders HJ, Hoppe B, Beck B, Tönshoff B, Höcker B, Wygoda S, Ehrich JH, Pape L, Konrad M, Rascher W, Dötsch J, Müller-Wiefel DE, Hoyer P; Study Group Members of the Gesellschaft für Pädiatrische Nephrologie; Knebelmann B, Pirson Y, Grunfeld JP, Niaudet P, Cochat P, Heidet L, Lebbah S, Torra R, Friede T, Lange K, Müller GA, Weber M. Gross O, et al. Among authors: knebelmann b. Kidney Int. 2012 Mar;81(5):494-501. doi: 10.1038/ki.2011.407. Epub 2011 Dec 14. Kidney Int. 2012. PMID: 22166847 Free article.

2

Autosomal dominant polycystic kidney disease: from molecular genetics to the patients.

Grünfeld JP, Chauveau D, Knebelmann B. Grünfeld JP, et al. Among authors: knebelmann b. Clin Investig. 1992 Sep;70(9):791-3. doi: 10.1007/BF00180749. Clin Investig. 1992. PMID: 1450633 Review.

3

Alport syndrome and diffuse leiomyomatosis: deletions in the 5' end of the COL4A5 collagen gene.

Antignac C, Zhou J, Sanak M, Cochat P, Roussel B, Deschênes G, Gros F, Knebelmann B, Hors-Cayla MC, Tryggvason K, et al. Antignac C, et al. Among authors: knebelmann b. Kidney Int. 1992 Nov;42(5):1178-83. doi: 10.1038/ki.1992.402. Kidney Int. 1992. PMID: 1453602 Free article.

4

Inherited kidney diseases: polycystic kidney disease and Alport syndrome.

Chauveau D, Knebelmann B, Grünfeld JP. Chauveau D, et al. Among authors: knebelmann b. Adv Intern Med. 1995;40:303-39. Adv Intern Med. 1995. PMID: 7747650 Review. No abstract available.

5

Autosomal recessive Alport syndrome: immunohistochemical study of type IV collagen chain distribution.

Gubler MC, Knebelmann B, Beziau A, Broyer M, Pirson Y, Haddoum F, Kleppel MM, Antignac C. Gubler MC, et al. Among authors: knebelmann b. Kidney Int. 1995 Apr;47(4):1142-7. doi: 10.1038/ki.1995.163. Kidney Int. 1995. PMID: 7783412 Free article.

6

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.

7

Molecular genetics of Alport syndrome: the clinical consequences.

Knebelmann B, Antignac C, Gubler MC, Grünfeld JP. Knebelmann B, et al. Nephrol Dial Transplant. 1993;8(8):677-9. doi: 10.1093/ndt/8.8.677. Nephrol Dial Transplant. 1993. PMID: 8414149 No abstract available.

8

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.

9

Spectrum of mutations in the COL4A5 collagen gene in X-linked Alport syndrome.

Knebelmann B, Breillat C, Forestier L, Arrondel C, Jacassier D, Giatras I, Drouot L, Deschênes G, Grünfeld JP, Broyer M, Gubler MC, Antignac C. Knebelmann B, et al. Am J Hum Genet. 1996 Dec;59(6):1221-32. Am J Hum Genet. 1996. PMID: 8940267 Free PMC article.

10

X-linked Alport syndrome: natural history in 195 families and genotype- phenotype correlations in males.

Jais JP, Knebelmann B, Giatras I, Marchi M, Rizzoni G, Renieri A, Weber M, Gross O, Netzer KO, Flinter F, Pirson Y, Verellen C, Wieslander J, Persson U, Tryggvason K, Martin P, Hertz JM, Schröder C, Sanak M, Krejcova S, Carvalho MF, Saus J, Antignac C, Smeets H, Gubler MC. Jais JP, et al. Among authors: knebelmann b. J Am Soc Nephrol. 2000 Apr;11(4):649-657. doi: 10.1681/ASN.V114649. J Am Soc Nephrol. 2000. PMID: 10752524

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