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

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

Lack of large, homozygous deletions of the nephronophthisis 1 region in Joubert syndrome type B. APN Study Group. Arbeitsgemeinschaft für Pädiatrische Nephrologie.

Hildebrandt F, Nothwang HG, Vossmerbäumer U, Springer C, Strahm B, Hoppe B, Keuth B, Fuchshuber A, Querfeld U, Neuhaus TJ, Brandis M. Hildebrandt F, et al. Among authors: brandis m. Pediatr Nephrol. 1998 Jan;12(1):16-9. doi: 10.1007/s004670050394. Pediatr Nephrol. 1998. PMID: 9502560

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: brandis m. J Am Soc Nephrol. 2001 Jan;12(1):107-113. doi: 10.1681/ASN.V121107. J Am Soc Nephrol. 2001. PMID: 11134256

5

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

6

The nephronophthisis complex: clinical and genetic aspects.

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

7

Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome.

Heeringa SF, Vlangos CN, Chernin G, Hinkes B, Gbadegesin R, Liu J, Hoskins BE, Ozaltin F, Hildebrandt F; Members of the APN Study Group. Heeringa SF, et al. Nephrol Dial Transplant. 2008 Nov;23(11):3527-33. doi: 10.1093/ndt/gfn271. Epub 2008 May 23. Nephrol Dial Transplant. 2008. PMID: 18503012 Free PMC article.

8

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

9

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

10

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.

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