Hildebrandt F - Search Results

1

Clinical and genetic evaluation of familial steroid-responsive nephrotic syndrome in childhood.

Fuchshuber A, Gribouval O, Ronner V, Kroiss S, Karle S, Brandis M, Hildebrandt F. Fuchshuber A, et al. Among authors: hildebrandt f. J Am Soc Nephrol. 2001 Feb;12(2):374-378. doi: 10.1681/ASN.V122374. J Am Soc Nephrol. 2001. PMID: 11158229

2

The nephronophthisis complex: clinical and genetic aspects.

Hildebrandt F, Waldherr R, Kutt R, Brandis M. Hildebrandt F, et al. Clin Investig. 1992 Sep;70(9):802-8. doi: 10.1007/BF00180751. Clin Investig. 1992. PMID: 1450635 Review.

3

Cyclosporine A for treatment of nephrotic syndromes.

Brandis M, Burghard R, Leititis J, Zimmerhackl B, Hildebrandt F, Helmchen U. Brandis M, et al. Among authors: hildebrandt f. Transplant Proc. 1988 Jun;20(3 Suppl 4):275-9. Transplant Proc. 1988. PMID: 3381283 No abstract available.

4

[Hereditary diseases of the kidney].

Hildebrandt F, Weber M, Brandis M. Hildebrandt F, et al. Internist (Berl). 1995 Mar;36(3):254-62. Internist (Berl). 1995. PMID: 7737818 Review. German. No abstract available.

5

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. Genomics. 1995 Jan 20;25(2):360-4. doi: 10.1016/0888-7543(95)80034-j. Genomics. 1995. PMID: 7789968

6

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. Cytogenet Cell Genet. 1996;73(3):235-9. doi: 10.1159/000134346. Cytogenet Cell Genet. 1996. PMID: 8697815

7

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. 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

8

Molecular genetic identification of families with juvenile nephronophthisis type 1: rate of progression to renal failure. APN Study Group. Arbeitsgemeinschaft für Pädiatrische Nephrologie.

Hildebrandt F, Strahm B, Nothwang HG, Gretz N, Schnieders B, Singh-Sawhney I, Kutt R, Vollmer M, Brandis M. Hildebrandt F, et al. Kidney Int. 1997 Jan;51(1):261-9. doi: 10.1038/ki.1997.31. Kidney Int. 1997. PMID: 8995741 Free article.

9

Probable Opitz trigonocephaly C syndrome with medulloblastoma.

Omran H, Hildebrandt F, Korinthenberg R, Brandis M. Omran H, et al. Among authors: hildebrandt f. Am J Med Genet. 1997 Apr 14;69(4):395-9. Am J Med Genet. 1997. PMID: 9098489

10

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. Nat Genet. 1997 Oct;17(2):149-53. doi: 10.1038/ng1097-149. Nat Genet. 1997. PMID: 9326933

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