Gretz N - Search Results

1

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

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. Among authors: gretz n. Kidney Int. 1997 Jan;51(1):261-9. doi: 10.1038/ki.1997.31. Kidney Int. 1997. PMID: 8995741 Free article.

3

Rate of deterioration of renal function in juvenile nephronophthisis.

Gretz N, Schärer K, Waldherr R, Strauch M. Gretz N, et al. Pediatr Nephrol. 1989 Jan;3(1):56-60. doi: 10.1007/BF00859627. Pediatr Nephrol. 1989. PMID: 2702089

4

Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis.

Olbrich H, Fliegauf M, Hoefele J, Kispert A, Otto E, Volz A, Wolf MT, Sasmaz G, Trauer U, Reinhardt R, Sudbrak R, Antignac C, Gretz N, Walz G, Schermer B, Benzing T, Hildebrandt F, Omran H. Olbrich H, et al. Among authors: gretz n. Nat Genet. 2003 Aug;34(4):455-9. doi: 10.1038/ng1216. Nat Genet. 2003. PMID: 12872122

5

Loss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia.

Bergmann C, Fliegauf M, Brüchle NO, Frank V, Olbrich H, Kirschner J, Schermer B, Schmedding I, Kispert A, Kränzlin B, Nürnberg G, Becker C, Grimm T, Girschick G, Lynch SA, Kelehan P, Senderek J, Neuhaus TJ, Stallmach T, Zentgraf H, Nürnberg P, Gretz N, Lo C, Lienkamp S, Schäfer T, Walz G, Benzing T, Zerres K, Omran H. Bergmann C, et al. Among authors: gretz n. Am J Hum Genet. 2008 Apr;82(4):959-70. doi: 10.1016/j.ajhg.2008.02.017. Epub 2008 Mar 27. Am J Hum Genet. 2008. PMID: 18371931 Free PMC article.

6

Phenotypic Spectrum of Children with Nephronophthisis and Related Ciliopathies.

König J, Kranz B, König S, Schlingmann KP, Titieni A, Tönshoff B, Habbig S, Pape L, Häffner K, Hansen M, Büscher A, Bald M, Billing H, Schild R, Walden U, Hampel T, Staude H, Riedl M, Gretz N, Lablans M, Bergmann C, Hildebrandt F, Omran H, Konrad M; Gesellschaft für Pädiatrische Nephrologie (GPN). König J, et al. Among authors: gretz n. Clin J Am Soc Nephrol. 2017 Dec 7;12(12):1974-1983. doi: 10.2215/CJN.01280217. Epub 2017 Nov 16. Clin J Am Soc Nephrol. 2017. PMID: 29146700 Free PMC article.

7

Natural course of the development of histological lesions after 5/6 nephrectomy.

Waldherr R, Gretz N. Waldherr R, et al. Among authors: gretz n. Contrib Nephrol. 1988;60:64-72. doi: 10.1159/000414791. Contrib Nephrol. 1988. PMID: 3345677 No abstract available.

8

Gender-dependent disease severity in autosomal polycystic kidney disease of rats.

Gretz N, Ceccherini I, Kränzlin B, Klöting I, Devoto M, Rohmeiss P, Hocher B, Waldherr R, Romeo G. Gretz N, et al. Kidney Int. 1995 Aug;48(2):496-500. doi: 10.1038/ki.1995.319. Kidney Int. 1995. PMID: 7564118 Free article.

9

Location of the first genetic locus, PKDr1, controlling autosomal dominant polycystic kidney disease in Han:SPRD cy/+ rat.

Bihoreau MT, Ceccherini I, Browne J, Kränzlin B, Romeo G, Lathrop GM, James MR, Gretz N. Bihoreau MT, et al. Among authors: gretz n. Hum Mol Genet. 1997 Apr;6(4):609-13. doi: 10.1093/hmg/6.4.609. Hum Mol Genet. 1997. PMID: 9097967

10

Acute renal failure after 5/6 nephrectomy: histological and functional changes.

Gretz N, Meisinger E, Waldherr R, Strauch M. Gretz N, et al. Contrib Nephrol. 1988;60:56-63. doi: 10.1159/000414790. Contrib Nephrol. 1988. PMID: 3345676 No abstract available.

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