Hildebrandt F - Search Results

1

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

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

[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.

4

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

5

A gene for familial juvenile nephronophthisis (recessive medullary cystic kidney disease) maps to chromosome 2p.

Antignac C, Arduy CH, Beckmann JS, Benessy F, Gros F, Medhioub M, Hildebrandt F, Dufier JL, Kleinknecht C, Broyer M, et al. Antignac C, et al. Among authors: hildebrandt f. Nat Genet. 1993 Apr;3(4):342-5. doi: 10.1038/ng0493-342. Nat Genet. 1993. PMID: 7981755

6

Mapping of a gene for familial juvenile nephronophthisis: refining the map and defining flanking markers on chromosome 2. APN Study Group.

Hildebrandt F, Singh-Sawhney I, Schnieders B, Centofante L, Omran H, Pohlmann A, Schmaltz C, Wedekind H, Schubotz C, Antignac C, et al. Hildebrandt F, et al. Am J Hum Genet. 1993 Dec;53(6):1256-61. Am J Hum Genet. 1993. PMID: 8250041 Free PMC article.

7

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

8

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

9

Report and abstracts of the Fourth International Workshop on Human Chromosome 2 Mapping 1996.

Spur NK, Bashir R, Bushby K, Cox A, Cox S, Hilde Brandt F, Hill N, Kao FT, Krols L, Marzella R, Miller N, Nothwang HG, Rocchi M, Sarfarazi M, Stratakis CA, Wallgren-Petterson C, Naylor S. Spur NK, et al. Cytogenet Cell Genet. 1996;73(4):255-73. doi: 10.1159/000134352. Cytogenet Cell Genet. 1996. PMID: 8751373 No abstract available.

10

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.

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