Hildebrandt F - Search Results

1

A gene locus for steroid-resistant nephrotic syndrome with deafness maps to chromosome 14q24.2.

Ruf RG, Wolf MT, Hennies HC, Lucke B, Zinn C, Varnholt V, Lichtenberger A, Pasch A, Imm A, Briese S, Lennert T, Fuchshuber A, Nurnberg P, Hildebrandt F. Ruf RG, et al. Among authors: hildebrandt f. J Am Soc Nephrol. 2003 Jun;14(6):1519-22. doi: 10.1097/01.asn.0000066141.55735.8d. J Am Soc Nephrol. 2003. PMID: 12761252

2

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

3

The gene for human fibronectin glomerulopathy maps to 1q32, in the region of the regulation of complement activation gene cluster.

Vollmer M, Jung M, Rüschendorf F, Ruf R, Wienker T, Reis A, Krapf R, Hildebrandt F. Vollmer M, et al. Among authors: hildebrandt f. Am J Hum Genet. 1998 Dec;63(6):1724-31. doi: 10.1086/302162. Am J Hum Genet. 1998. PMID: 9837825 Free PMC article.

4

Hereditary isolated renal magnesium loss maps to chromosome 11q23.

Meij IC, Saar K, van den Heuvel LP, Nuernberg G, Vollmer M, Hildebrandt F, Reis A, Monnens LA, Knoers NV. Meij IC, et al. Among authors: hildebrandt f. Am J Hum Genet. 1999 Jan;64(1):180-8. doi: 10.1086/302199. Am J Hum Genet. 1999. PMID: 9915957 Free PMC article.

5

Evidence of further genetic heterogeneity in autosomal dominant medullary cystic kidney disease.

Kroiss S, Huck K, Berthold S, Rüschendorf F, Scolari F, Caridi G, Ghiggeri GM, Hildebrandt F, Fuchshuber A. Kroiss S, et al. Among authors: hildebrandt f. Nephrol Dial Transplant. 2000 Jun;15(6):818-21. doi: 10.1093/ndt/15.6.818. Nephrol Dial Transplant. 2000. PMID: 10831633

6

Antenatal Bartter syndrome with sensorineural deafness: refinement of the locus on chromosome 1p31.

Vollmer M, Jeck N, Lemmink HH, Vargas R, Feldmann D, Konrad M, Beekmann F, van Den Heuvel LP, Deschenes G, Guay-Woodford LM, Antignac C, Seyberth HW, Hildebrandt F, Knoers NV. Vollmer M, et al. Among authors: hildebrandt f. Nephrol Dial Transplant. 2000 Jul;15(7):970-4. doi: 10.1093/ndt/15.7.970. Nephrol Dial Transplant. 2000. PMID: 10862633

7

Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome.

Konrad M, Vollmer M, Lemmink HH, VAN DEN Heuvel LPWJ, Jeck N, Vargas-Poussou R, Lakings A, Ruf R, Deschênes G, Antignac C, Guay-Woodford L, Knoers NVAM, Seyberth HW, Feldmann D, Hildebrandt F. Konrad M, et al. Among authors: hildebrandt f. J Am Soc Nephrol. 2000 Aug;11(8):1449-1459. doi: 10.1681/ASN.V1181449. J Am Soc Nephrol. 2000. PMID: 10906158

8

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

9

Improved strategy for molecular genetic diagnostics in juvenile nephronophthisis.

Heninger E, Otto E, Imm A, Caridi G, Hildebrandt F. Heninger E, et al. Among authors: hildebrandt f. Am J Kidney Dis. 2001 Jun;37(6):1131-9. doi: 10.1053/ajkd.2001.24514. Am J Kidney Dis. 2001. PMID: 11382680

10

Refinement of the gene locus for autosomal dominant medullary cystic kidney disease type 1 (MCKD1) and construction of a physical and partial transcriptional map of the region.

Fuchshuber A, Kroiss S, Karle S, Berthold S, Huck K, Burton C, Rahman N, Koptides M, Deltas C, Otto E, Rüschendorf F, Feest T, Hildebrandt F. Fuchshuber A, et al. Among authors: hildebrandt f. Genomics. 2001 Mar 15;72(3):278-84. doi: 10.1006/geno.2000.6486. Genomics. 2001. PMID: 11401443

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