Yazar "Tabel, Y." için listeleme

Effects of genetic polymorphisms of the renin-angiotensin system in children with nephrotic syndrome

Tabel, Y.; Berdeli, A.; Mir, S.; Serdaroǧlu, E.; Yilmaz, E. (2005)

Background. The renin-angiotensin system (RAS) has been considered to be responsible for the pathogenesis or progression of many diseases which may or may not be related to kidney. Genetic polymorphisms of the various ...

Is presence of hypertension in obese children correlate with the criteria of metabolic syndrome?

Mir, S.; Tabel, Y.; Darcan, S. (2007)

In this article, we will describe the presence of metabolic syndrome and its components in a group of hypertensive and obese adolescents. The study presented here was conducted on 20 patients (10 boys) presented with ...

NPHS2 (podicin) mutations in Turkish children with idiopathic nephrotic syndrome

Berdeli, A.; Mir, S.; Yavascan, O.; Serdaroglu, E.; Bak, M.; Aksu, N.; Oner, A.; Anarat, A.; Donmez, O.; Yildiz, N.; Sever, L.; Tabel, Y.; Dusunsel, R.; Sonmez, F.; Cakar, N. (2007)

The podocin (NPHS2) gene encodes podocin protein, which has an important role in glomerular ultrafiltration and controlling slit membrane permeability. The detection of an NPHS2 mutation affects the treatment plan for ...

Association of TLR2 gene Arg753Gln polymorphism with urinary tract infection in children

Tabel, Y.; Berdeli, A.; Mir, S. (2007)

The aim of this study is to investigate Arg753Gln allele polymorphisms of toll-like receptor-2 (TLR2) gene distribution, allele frequency in urinary tract infection (UTI) and genotype-phenotype association of TLR2 gene in ...

The role of ghrelin in weight gain and growth in epileptic children using valproate

Gungor, S.; Yücel, G.; Akinci, A.; Tabel, Y.; Ozerol, I.H.; Yologlu, S. (2007)

Ghrelin is a major hormone, regulating the energy balance of the body. Weight gain is a significant side effect of valproic acid, which has not been clearly identified pathogenetically. The aim of this study was to investigate ...

Neuroimaging findings in hyperargininemia

Güngör, S.; Akinci, A.; Firat, A.K.; Tabel, Y.; Alkan, A. (2008)

In hyperarginenemia, there is a defect in argininase enzyme, which is a catalyzer of urea cycle. Though the pathogenesis of neuronal damage in hyperargininemia is not clear, high serum and cerebrospinal fluid arginine ...

Is edema in minimal change disease of childhood really hypovolemic?

Tabel, Y.; Mungan, I.; Karakurt, C.; Kocak, G.; Gungor, S. (2008)

Objectives: In this study, we aimed to find out whether children with minimal change disease can be classified as hypervolemic by objective measures. Methods: Eighteen children with minimal change disease diagnosed at our ...

Clinical and demographic characteristics of children with urolithiasis: Single-center experience from eastern Turkey

Tabel, Y.; Akin, I.M.; Tekin, S. (2009)

Objective: To evaluate the clinical and demographic findings of children with urolithiasis in eastern Turkey. Methods: We retrospectively reviewed the medical records of 67 children with urolithiasis for clinical and ...

Primary lymphoedema at an unusual location triggered by nephrotic syndrome

Tabel, Y.; Mungan, I.; Sigirci, A.; Gungor, S. (2009)

Introduction: Lymphoedema results from impaired lymphatic transport leading to the pathologic accumulation of protein-rich lymphatic fluid in the interstitial space, most commonly in the extremities. Primary lymphoedema, ...

Antibodies to borna disease virus in children with attention deficit-hyperactivity disorder borna disease virus serology in attention deficit-hyperactivity disorder

Özcan, Ö.; Güngör, S.; Helps, C.R.; Turan, N.; Tabel, Y.; Saget, H.; Yilmaz, H. (2009)

Borna disease virus (BDV) causes behavioral disorders in rats infected in the newborn period. We investigated BDV serology in children with attention deficit hyperactivity disorder (ADHD). Method: Ninety-nine children with ...

Fludrocortisone therapy in a newborn with cerebral salt wasting due to hypernatremia and severe hyperbilirubinemia

Karadag, A.; Tabel, Y.; Dogan, D.G.; Aktas, M.; Aslan, M.; Dogan, M. (2010)

Ultrasonographic screening of newborns for congenital anomalies of the kidney and the urinary tracts

Tabel, Y.; Haskologlu, Z.S.; Karakas, H.M.; Yakinci, C. (2010)

Purpose: To search for the efficiency of scanning the newborns with routine urinary system ultrasonography. Materials and Methods: Urinary ultrasonography has been carried out on 721 infants born in or brought to our ...

Interleukin 8 gene 2767 A/G polymorphism is associated with increased risk of nephritis in children with Henoch-Schönlein purpura

Tabel, Y.; Mir, S.; Berdeli, A. (2012)

The objective of this study is to investigate the association between IL-8 gene 2767 G/A polymorphism and clinical features, kidney involvement and prognosis in childhood Henoch Schnölein purpura (HSP). A total of 115 ...

Celiac disease in children with urolithiasis

Menekşe, E.; Selimoǧlu, M.A.; Temel, I.; Tabel, Y.; Gürgöze, M. (2012)

There are a few studies suggesting a relationship between celiac disease (CD) and kidney disease, but no study has investigated CD in patients with urolithiasis. In this study, we aimed to determine the prevalence of CD ...

Clinical features of children with henoch-schonlein: Purpura risk factors associated with renal involvement

Tabel, Y.; Inanc, F.C.; Dogan, D.G.; Elmas, A.T. (2012)

Introduction. This study aimed to evaluate renal involvement and factors affecting the prognosis in patients with Henoch-Schonlein purpura (HSP). Materials and Methods. The outcomes of 107 children diagnosed with HSP who ...

Serum cystatin C predicts acute kidney injury in preterm neonates with respiratory distress syndrome

Elmas, A.T.; Tabel, Y.; Elmas, O.N. (2013)

Background: We aimed to compare serum cystatin C levels (sCysC) in preterm neonates with respiratory distress syndrome (RDS) with a control group and to investigate whether it could be used as a predictor for acute kidney ...

Short- and long-term efficacy of levamisole in children with steroid-sensitive nephrotic syndrome

Elmas, A.T.; Tabel, Y.; Elmas, O.N. (2013)

Purpose: In this study, we aimed to evaluate short- and long-term effects of levamisole therapy in steroid-sensitive nephrotic syndrome (SSNS) in children. Methods: The study consisted of 29 SSNS patients who had been ...

Lack of association between macrophage migration inhibitory factor gene promoter (-173 G/C) polymorphism and childhood Henoch-Schönlein purpura in Turkish patients

Nalbantoglu, S.; Tabel, Y.; Mir, S.; Berdeli, A. (2013)

Henoch-Schönlein purpura (HSP) is a small-vessel vasculitis of autoimmune hypersensitivity with rash, arthritis, abdominal pain and renal involvements. Macrophage migration inhibitory factor (MIF) is a immunoregulatory ...

Association between RAS gene polymorphisms (ACE I/D, AGT M235T) and Henoch-Schönlein purpura in a Turkish population

Nalbantoglu, S.; Tabel, Y.; Mir, S.; Serdaroǧlu, E.; Berdeli, A. (2013)

Henoch-Schönlein purpura (HSP) is a small-vessel vasculitis of autoimmune hypersensitivity, and renin-angiotensin system (RAS) regulates vascular homeostasis and inflammation with activation of cytokine release. Thus, we ...

Is Urolithiasis in Children Associated With Obesity or Malnutrition?

Selimoĝlu, M.A.; Menekşe, E.; Tabel, Y. (2013)

Background: Although it is known that obesity predisposes to urolithiasis, a tendency for malnutrition in children with urolithiasis owing to recurrent urinary infections and abdominal pain also makes sense. Aims: In this ...

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