Hildebrandt F - Search Results

1

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.

2

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.

3

Identification of a new gene locus for adolescent nephronophthisis, on chromosome 3q22 in a large Venezuelan pedigree.

Omran H, Fernandez C, Jung M, Häffner K, Fargier B, Villaquiran A, Waldherr R, Gretz N, Brandis M, Rüschendorf F, Reis A, Hildebrandt F. Omran H, et al. Among authors: hildebrandt f. Am J Hum Genet. 2000 Jan;66(1):118-27. doi: 10.1086/302705. Am J Hum Genet. 2000. PMID: 10631142 Free PMC article.

4

Human adolescent nephronophthisis: gene locus synteny with polycystic kidney disease in pcy mice.

Omran H, Häffner K, Burth S, Fernandez C, Fargier B, Villaquiran A, Nothwang HG, Schnittger S, Lehrach H, Woo D, Brandis M, Sudbrak R, Hildebrandt F. Omran H, et al. Among authors: hildebrandt f. J Am Soc Nephrol. 2001 Jan;12(1):107-113. doi: 10.1681/ASN.V121107. J Am Soc Nephrol. 2001. PMID: 11134256

5

Identification of a gene locus for Senior-Løken syndrome in the region of the nephronophthisis type 3 gene.

Omran H, Sasmaz G, Häffner K, Volz A, Olbrich H, Melkaoui R, Otto E, Wienker TF, Korinthenberg R, Brandis M, Antignac C, Hildebrandt F. Omran H, et al. Among authors: hildebrandt f. J Am Soc Nephrol. 2002 Jan;13(1):75-79. doi: 10.1681/ASN.V13175. J Am Soc Nephrol. 2002. PMID: 11752023

6

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

7

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

8

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: hildebrandt f. Nephrol Dial Transplant. 1998 Aug;13(8):1955-7. doi: 10.1093/ndt/13.8.1955. Nephrol Dial Transplant. 1998. PMID: 9719147

9

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

10

[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.

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