Ibolya Haszon
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Explore the profile of Ibolya Haszon including associated specialties, affiliations and a list of published articles.
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10
Citations
81
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Recent Articles
1.
Kovacs G, Kalmar T, Endreffy E, Ondrik Z, Ivanyi B, Rikker C, et al.
PLoS One
. 2016 Mar;
11(3):e0149241.
PMID: 26934356
Alport syndrome (AS) is an inherited type IV collagen nephropathies characterized by microscopic hematuria during early childhood, the development of proteinuria and progression to end-stage renal disease. Since choosing the...
2.
Endreffy E, Ondrik Z, Ivanyi B, Maroti Z, Bereczki C, Haszon I, et al.
Mol Cell Probes
. 2010 Oct;
25(1):28-34.
PMID: 20951199
The Col4A3, Col4A4 and Col4A5 collagen type IV genes are found to be mutated in Col IV nephropathy. In males with a mutation in the Col4A5 gene (X-linked Alport syndrome:...
3.
Sumegi V, Haszon I, Bereczki C, Papp F, Turi S
Pediatr Nephrol
. 2008 Mar;
23(7):1085-92.
PMID: 18324421
A retrospective study was made on 37 children with idiopathic nephrotic syndrome (INS). At the beginning, all patients were steroid sensitive but received more than one steroid course (median 4)....
4.
Barath A, Nemeth I, Karg E, Endreffy E, Bereczki C, Gellen B, et al.
Kidney Blood Press Res
. 2006 Aug;
29(3):144-51.
PMID: 16912512
Background/aims: Paraoxonase 1 (PON1) is associated with high-density lipoproteins in the plasma, and is capable of hydrolysing oxidized lipids and preventing the oxidation of low-density lipoproteins. Oxidative stress and the...
5.
Barath A, Turi S, Nemeth I, Bereczki C, Gellen B, Haszon I, et al.
Pediatr Nephrol
. 2006 Aug;
21(10):1419-25.
PMID: 16896999
Obesity-induced hypertension and essential hypertension in lean patients are two different forms of hypertension. The main goal of this study was to test whether there are differences in biochemical parameters...
6.
Endreffy E, Ondrik Z, Kemeny E, Vas Z, Maroti Z, Lencse G, et al.
Orv Hetil
. 2006 Feb;
146(52):2647-53.
PMID: 16468607
Introduction: Collagen type IV nephropathy includes the Goodpasture syndrome, thin basement membrane nephropathy and the Alport syndrome. Mutations in the coding Col(IV)A3/A4 and Col(IV)A5 genes are probable causes of the...
7.
Sumegi V, Haszon I, Ivanyi B, Bereczki C, Papp F, Turi S
Pediatr Nephrol
. 2004 Nov;
19(12):1354-60.
PMID: 15517419
The effects of levamisole treatment on long-term outcome were evaluated in a retrospective study of frequently-relapsing (FRNS, n=15), steroid-dependent (SDNS, n=13), and steroid-resistant (SRNS, n=6) nephrotic syndrome in 34 children...
8.
Haszon I, Papp F, Kovacs J, Bors M, Nemeth I, Bereczki C, et al.
Eur J Pediatr
. 2003 Apr;
162(6):385-90.
PMID: 12684895
Unlabelled: A group of 35 patients (median age 15.5 years, range 8-17 years) with juvenile essential hypertension, 15 with body mass index (BMI kg/m(2)) <25 and 20 with BMI >25,...
9.
Papp F, Friedman A, Bereczki C, Haszon I, Kiss E, Endreffy E, et al.
Pediatr Nephrol
. 2003 Feb;
18(2):150-4.
PMID: 12579405
The M235T polymorphism of the angiotensinogen (ANG) gene, the I/D polymorphism of the angiotensin converting enzyme (ACE) gene, and the A1166C polymorphism of the angiotensin II type 1 receptor (AT1R)...
10.
Haszon I, Friedman A, Papp F, Bereczki C, Baji S, Bodrogi T, et al.
Pediatr Nephrol
. 2002 Dec;
17(12):1027-31.
PMID: 12478352
The objective of this study was to investigate whether mutations of the renin-angiotensin system genes are involved in primary vesicoureteric reflux (VUR) and VUR-associated renal scarring. The M235T polymorphism of...