Endreffy E - Search Results

1

Efficient Targeted Next Generation Sequencing-Based Workflow for Differential Diagnosis of Alport-Related Disorders.

Kovács G, Kalmár T, Endreffy E, Ondrik Z, Iványi B, Rikker C, Haszon I, Túri S, Sinkó M, Bereczki C, Maróti Z. Kovács G, et al. Among authors: endreffy e. PLoS One. 2016 Mar 2;11(3):e0149241. doi: 10.1371/journal.pone.0149241. eCollection 2016. PLoS One. 2016. PMID: 26934356 Free PMC article.

2

[Collagen type IV nephropathy: from thin basement membrane nephropathy to Alport syndrome].

Endreffy E, Ondrik Z, Kemény E, Vas Z, Maróti Z, Lencse G, Bereczki C, Haszon I, Túri S, Iványi B. Endreffy E, et al. Orv Hetil. 2005 Dec 25;146(52):2647-53. Orv Hetil. 2005. PMID: 16468607 Hungarian.

3

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. 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

4

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. 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

5

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: endreffy e. Pediatr Nephrol. 2003 Feb;18(2):150-4. doi: 10.1007/s00467-002-1032-x. Epub 2002 Dec 18. Pediatr Nephrol. 2003. PMID: 12579405

6

Mitochondrial mutation as a probable causative factor in familial progressive tubulointerstitial nephritis.

Zsurka G, Ormos J, Iványi B, Túri S, Endreffy E, Magyari M, Sonkodi S, Venetianer P. Zsurka G, et al. Among authors: endreffy e. Hum Genet. 1997 Apr;99(4):484-7. doi: 10.1007/s004390050393. Hum Genet. 1997. PMID: 9099838

7

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: endreffy e. 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.

8

Childhood membranous nephropathy, circulating antibodies to the 58-kD TIN antigen, and anti-tubular basement membrane nephritis: an 11-year follow-up.

Iványi B, Haszon I, Endreffy E, Szenohradszky P, Petri IB, Kalmár T, Butkowski RJ, Charonis AS, Túri S. Iványi B, et al. Among authors: endreffy e. Am J Kidney Dis. 1998 Dec;32(6):1068-74. doi: 10.1016/s0272-6386(98)70085-x. Am J Kidney Dis. 1998. PMID: 9856526 Review.

9

Increased heme oxygenase-1 expression in premature infants with respiratory distress syndrome.

Farkas I, Maróti Z, Katona M, Endreffy E, Monostori P, Máder K, Túri S. Farkas I, et al. Among authors: endreffy e. Eur J Pediatr. 2008 Dec;167(12):1379-83. doi: 10.1007/s00431-008-0673-6. Epub 2008 Feb 27. Eur J Pediatr. 2008. PMID: 18301921

10

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: endreffy e. Pediatr Nephrol. 2004 Apr;19(4):426-31. doi: 10.1007/s00467-003-1384-x. Epub 2004 Feb 24. Pediatr Nephrol. 2004. PMID: 14986081

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