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The nephronophthisis complex: clinical and genetic aspects.
Hildebrandt F, Waldherr R, Kutt R, Brandis M. Hildebrandt F, et al. Among authors: brandis m. Clin Investig. 1992 Sep;70(9):802-8. doi: 10.1007/BF00180751. Clin Investig. 1992. PMID: 1450635 Review.
Cytostatics--induced tubular toxicity.
Brandis M, von der Hardt K, Zimmerhackl RB, Mohrmann M, Leititis J. Brandis M, et al. Clin Investig. 1993 Oct;71(10):855-7. doi: 10.1007/BF00190337. Clin Investig. 1993. PMID: 8305848 Review. No abstract available.
[Nephrologic aspects of tumor diseases in children].
Brandis M. Brandis M. Monatsschr Kinderheilkd. 1989 Oct;137(10):643-8. Monatsschr Kinderheilkd. 1989. PMID: 2555707 Review. German.
A novel gene encoding an SH3 domain protein is mutated in nephronophthisis type 1.
Hildebrandt F, Otto E, Rensing C, Nothwang HG, Vollmer M, Adolphs J, Hanusch H, Brandis M. Hildebrandt F, et al. Among authors: brandis m. Nat Genet. 1997 Oct;17(2):149-53. doi: 10.1038/ng1097-149. Nat Genet. 1997. PMID: 9326933
Autosomal dominant medullary cystic kidney disease: evidence of gene locus heterogeneity.
Fuchshuber A, Deltas CC, Berthold S, Stavrou C, Vollmer M, Burton C, Feest T, Krieter D, Gal A, Brandis M, Pierides A, Hildebrandt F. Fuchshuber A, et al. Among authors: brandis m. Nephrol Dial Transplant. 1998 Aug;13(8):1955-7. doi: 10.1093/ndt/13.8.1955. Nephrol Dial Transplant. 1998. PMID: 9719147
Physical mapping of the gene for juvenile nephronophthisis (NPH1) by construction of a complete YAC contig of 7 Mb on chromosome 2q13.
Hildebrandt F, Cybulla M, Strahm B, Nothwang HG, Singh-Sawhney I, Berz K, Nicklin M, Reiner O, Brandis M. Hildebrandt F, et al. Among authors: brandis m. Cytogenet Cell Genet. 1996;73(3):235-9. doi: 10.1159/000134346. Cytogenet Cell Genet. 1996. PMID: 8697815
Refined genetic mapping of a gene for familial juvenile nephronophthisis (NPH1) and physical mapping of linked markers. APN Study Group.
Hildebrandt F, Singh-Sawhney I, Schnieders B, Papenfuss T, Brandis M. Hildebrandt F, et al. Among authors: brandis m. Genomics. 1995 Jan 20;25(2):360-4. doi: 10.1016/0888-7543(95)80034-j. Genomics. 1995. PMID: 7789968
Glomerulopathy associated with predominant fibronectin deposits: exclusion of the genes for fibronectin, villin and desmin as causative genes.
Hildebrandt F, Strahm B, Prochoroff A, Cybulla M, Gemperle O, Krapf R, Brandis M. Hildebrandt F, et al. Among authors: brandis m. Am J Med Genet. 1996 May 3;63(1):323-7. doi: 10.1002/(SICI)1096-8628(19960503)63:1<323::AID-AJMG54>3.0.CO;2-M. Am J Med Genet. 1996. PMID: 8723129
Renal involvement in tuberous sclerosis complex: a retrospective survey.
Zimmerhackl LB, Rehm M, Kaufmehl K, Kurlemann G, Brandis M. Zimmerhackl LB, et al. Among authors: brandis m. Pediatr Nephrol. 1994 Aug;8(4):451-7. doi: 10.1007/BF00856529. Pediatr Nephrol. 1994. PMID: 7947038
Renal proximal and distal tubular function is attenuated in diabetes mellitus type 1 as determined by the renal excretion of alpha 1-microglobulin and Tamm-Horsfall protein.
Pfleiderer S, Zimmerhackl LB, Kinne R, Manz F, Schuler G, Brandis M. Pfleiderer S, et al. Among authors: brandis m. Clin Investig. 1993 Dec;71(12):972-7. doi: 10.1007/BF00180026. Clin Investig. 1993. PMID: 7510155 Clinical Trial.
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