Túri S - Search Results

1

ACE gene polymorphism and renal scarring in primary vesicoureteric reflux.

Haszon I, Friedman AL, Papp F, Bereczki C, Baji S, Bodrogi T, Károly E, Endreffy E, Túri S. Haszon I, et al. Among authors: turi s. Pediatr Nephrol. 2002 Dec;17(12):1027-31. doi: 10.1007/s00467-002-0968-1. Epub 2002 Nov 14. Pediatr Nephrol. 2002. PMID: 12478352 Clinical Trial.

2

Renin-angiotensin gene polymorphism in children with uremia and essential hypertension.

Papp F, Friedman AL, Bereczki C, Haszon I, Kiss E, Endreffy E, Túri S. Papp F, et al. Among authors: turi s. Pediatr Nephrol. 2003 Feb;18(2):150-4. doi: 10.1007/s00467-002-1032-x. Epub 2002 Dec 18. Pediatr Nephrol. 2003. PMID: 12579405

3

Different pathomechanisms of essential and obesity-associated hypertension in adolescents.

Baráth A, Túri S, Németh I, Bereczki C, Gellén B, Haszon I, Monostori P. Baráth A, et al. Among authors: turi s. Pediatr Nephrol. 2006 Oct;21(10):1419-25. doi: 10.1007/s00467-006-0215-2. Epub 2006 Aug 8. Pediatr Nephrol. 2006. PMID: 16896999 Clinical Trial.

4

Heme oxygenase 1 expression in young uremic patients on hemodialysis.

Maróti Z, Németh I, Túri S, Karg E, Ugocsai P, Endreffy E. Maróti Z, et al. Among authors: turi s. Pediatr Nephrol. 2004 Apr;19(4):426-31. doi: 10.1007/s00467-003-1384-x. Epub 2004 Feb 24. Pediatr Nephrol. 2004. PMID: 14986081

5

Long-term effects of levamisole treatment in childhood nephrotic syndrome.

Sümegi V, Haszon I, Iványi B, Bereczki C, Papp F, Túri S. Sümegi V, et al. Among authors: turi s. Pediatr Nephrol. 2004 Dec;19(12):1354-60. doi: 10.1007/s00467-004-1608-8. Pediatr Nephrol. 2004. PMID: 15517419

6

Roles of paraoxonase and oxidative stress in adolescents with uraemic, essential or obesity-induced hypertension.

Baráth A, Németh I, Karg E, Endreffy E, Bereczki C, Gellén B, Haszon I, Túri S. Baráth A, et al. Among authors: turi s. Kidney Blood Press Res. 2006;29(3):144-51. doi: 10.1159/000095124. Epub 2006 Aug 10. Kidney Blood Press Res. 2006. PMID: 16912512

7

Long-term follow-up after cyclophosphamide and cyclosporine-A therapy in steroid-dependent and -resistant nephrotic syndrome.

Sümegi V, Haszon I, Bereczki C, Papp F, Túri S. Sümegi V, et al. Among authors: turi s. Pediatr Nephrol. 2008 Jul;23(7):1085-92. doi: 10.1007/s00467-008-0771-8. Epub 2008 Mar 7. Pediatr Nephrol. 2008. PMID: 18324421

8

Usefulness of combined genetic data in Hungarian families affected by autosomal dominant polycystic kidney disease.

Endreffy E, Maróti Z, Bereczki C, Túri S. Endreffy E, et al. Among authors: turi s. Mol Cell Probes. 2009 Feb;23(1):39-43. doi: 10.1016/j.mcp.2008.11.001. Epub 2008 Nov 21. Mol Cell Probes. 2009. PMID: 19056484

9

Collagen type IV nephropathy: genetic heterogeneity examinations in affected Hungarian families.

Endreffy E, Ondrik Z, Iványi B, Maróti Z, Bereczki C, Haszon I, Györke Z, Worum E, Németh K, Rikker C, Ökrös Z, Túri S. Endreffy E, et al. Among authors: turi s. Mol Cell Probes. 2011 Feb;25(1):28-34. doi: 10.1016/j.mcp.2010.10.001. Epub 2010 Oct 14. Mol Cell Probes. 2011. PMID: 20951199

10

The effect of erythropoietin on the cellular defence mechanism of red blood cells in children with chronic renal failure.

Túri S, Németh I, Varga I, Bodrogi T, Matkovics B. Túri S, et al. Pediatr Nephrol. 1992 Nov;6(6):536-41. doi: 10.1007/BF00866497. Pediatr Nephrol. 1992. PMID: 1482641

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