Brandis M - Search Results

1

Novel molecular variants of the Na-K-2Cl cotransporter gene are responsible for antenatal Bartter syndrome.

Vargas-Poussou R, Feldmann D, Vollmer M, Konrad M, Kelly L, van den Heuvel LP, Tebourbi L, Brandis M, Karolyi L, Hebert SC, Lemmink HH, Deschênes G, Hildebrandt F, Seyberth HW, Guay-Woodford LM, Knoers NV, Antignac C. Vargas-Poussou R, et al. Among authors: brandis m. Am J Hum Genet. 1998 Jun;62(6):1332-40. doi: 10.1086/301872. Am J Hum Genet. 1998. PMID: 9585600 Free PMC article.

2

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: brandis m. J Am Soc Nephrol. 2002 Jan;13(1):75-79. doi: 10.1681/ASN.V13175. J Am Soc Nephrol. 2002. PMID: 11752023

3

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

4

Probable Opitz trigonocephaly C syndrome with medulloblastoma.

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

5

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: brandis m. J Am Soc Nephrol. 2001 Feb;12(2):374-378. doi: 10.1681/ASN.V122374. J Am Soc Nephrol. 2001. PMID: 11158229

6

[Hereditary diseases of the kidney].

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

7

Confirmation of the ATP6B1 gene as responsible for distal renal tubular acidosis.

Ruf R, Rensing C, Topaloglu R, Guay-Woodford L, Klein C, Vollmer M, Otto E, Beekmann F, Haller M, Wiedensohler A, Leumann E, Antignac C, Rizzoni G, Filler G, Brandis M, Weber JL, Hildebrandt F. Ruf R, et al. Among authors: brandis m. Pediatr Nephrol. 2003 Feb;18(2):105-9. doi: 10.1007/s00467-002-1018-8. Epub 2002 Dec 18. Pediatr Nephrol. 2003. PMID: 12579397

8

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: brandis m. Am J Hum Genet. 2000 Jan;66(1):118-27. doi: 10.1086/302705. Am J Hum Genet. 2000. PMID: 10631142 Free PMC article.

9

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

10

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

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