Bereczki C - Search Results

1

Comprehensive genetic testing in children with a clinical diagnosis of ARPKD identifies phenocopies.

Szabó T, Orosz P, Balogh E, Jávorszky E, Máttyus I, Bereczki C, Maróti Z, Kalmár T, Szabó AJ, Reusz G, Várkonyi I, Marián E, Gombos É, Orosz O, Madar L, Balla G, Kappelmayer J, Tory K, Balogh I. Szabó T, et al. Among authors: bereczki c. Pediatr Nephrol. 2018 Oct;33(10):1713-1721. doi: 10.1007/s00467-018-3992-5. Epub 2018 Jun 28. Pediatr Nephrol. 2018. PMID: 29956005

2

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: bereczki c. 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.

3

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

4

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: bereczki c. 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

5

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: bereczki c. 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

6

The role of complement in Streptococcus pneumoniae-associated haemolytic uraemic syndrome.

Szilágyi A, Kiss N, Bereczki C, Tálosi G, Rácz K, Túri S, Györke Z, Simon E, Horváth E, Kelen K, Reusz GS, Szabó AJ, Tulassay T, Prohászka Z. Szilágyi A, et al. Among authors: bereczki c. Nephrol Dial Transplant. 2013 Sep;28(9):2237-45. doi: 10.1093/ndt/gft198. Epub 2013 Jun 19. Nephrol Dial Transplant. 2013. PMID: 23787556

7

Novel frameshift mutation in the CHD7 gene associated with CHARGE syndrome with preaxial polydactyly.

Surányi A, Maróti Z, Tálosi G, Kalmár T, Kaiser L, Bereczki C, Pál A, Keresztúri A. Surányi A, et al. Among authors: bereczki c. Clin Dysmorphol. 2016 Jul;25(3):98-100. doi: 10.1097/MCD.0000000000000120. Clin Dysmorphol. 2016. PMID: 26901670 No abstract available.

8

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: bereczki c. PLoS One. 2016 Mar 2;11(3):e0149241. doi: 10.1371/journal.pone.0149241. eCollection 2016. PLoS One. 2016. PMID: 26934356 Free PMC article.

9

Diffuse mesangial sclerosis in a PDSS2 mutation-induced coenzyme Q10 deficiency.

Iványi B, Rácz GZ, Gál P, Brinyiczki K, Bódi I, Kalmár T, Maróti Z, Bereczki C. Iványi B, et al. Among authors: bereczki c. Pediatr Nephrol. 2018 Mar;33(3):439-446. doi: 10.1007/s00467-017-3814-1. Epub 2017 Oct 14. Pediatr Nephrol. 2018. PMID: 29032433

10

Co-occurrence of mutations in FOXP1 and PTCH1 in a girl with extreme megalencephaly, callosal dysgenesis and profound intellectual disability.

Zombor M, Kalmár T, Maróti Z, Zimmermann A, Máté A, Bereczki C, Sztriha L. Zombor M, et al. Among authors: bereczki c. J Hum Genet. 2018 Nov;63(11):1189-1193. doi: 10.1038/s10038-018-0508-x. Epub 2018 Sep 4. J Hum Genet. 2018. PMID: 30181650 Free article.

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