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Yazar "Tabel, Y" için Araştırma Çıktıları | Wos İndeksli Yayınlar Koleksiyonu listeleme

Toplam kayıt 75, listelenen: 1-20

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Effects of genetic polymorphisms of the renin-angiotensin system in

Tabel, Y; Berdeli, A; Mir, S; Serdaroglu, 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 ...
NPHS2 (podicin) mutations in Turkish children with idiopathic nephrotic

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)

dThe 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 ...
The role of ghrelin in weight gain and growth in epileptic children

Gungor, S; Yucel, G; Akinci, A; Tabel, Y; Ozerol, IH; 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 ...
Association of TLR2 gene Arg753Gln polymorphism with urinary tract

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 ...
Is presence of hypertension in obese children correlate with the

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 ...
Case Study of Bardet-Biedl Syndrome with Fetal Lobulation and Focal

Tabel, Y; Akin, LM; Karadag, N; Akinci, A (2008)

Bardet-Biedl syndrome is a genetic autosomal recessive disease characterized by abdominal obesity, mental retardation, dysmorphic extremities, retinal dystrophy or pigmentary retinopathy, hypogonadism or hypogenitalism, ...
Neuroimaging findings in hyperargininemia

Gungor, S; Akinci, A; Firat, AK; 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.
Experience with Levamisole in Children with Frequently Relapsing and

Tabel, Y (2008)

In this manuscript; we aimed to report our experience with levamisole in frequently relapsing and/or steroid-dependent idiopathic nephrotic syndrome of childhood. Classical treatment option of idiopathic nephrotic syndrome ...
Primary Lymphoedema at an Unusual Location Triggered by Nephrotic

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

Ozcan, O; Gungor, S; Helps, CR; 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).
Clinical and Demographic Characteristics of Children with Urolithiasis:

Tabel, Y; Akin, IM; 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 ...
Fludrocortisone therapy in a newborn with cerebral salt wasting due to

Karadag, A; Tabel, Y; Dogan, DG; Aktas, M; Aslan, M; Dogan, M (2010)
Interleukin 8 Gene 2767 A/G Polymorphism Is Associated with Increased

Tabel, Y; Mir, S; Berdeli, A (2010)
REVERSIBLE POSTERIOR LEUCOENCEPHALOPATHY IN AN 11 YEAR-OLD MALE CHILD

Tabel, Y; Akin, IM; Gungor, S; Karakurt, C; Ozgen, U (2010)

Systemic lupus erythematosus is a chronic inflammatory disease characterized by highly diverse clinical manifestations. The major organ system involvements in childhood systemic lupus erythematosus are similar to those ...
Effects of Total Parenteral Nutrition on Renal Function in Preterm

Tabel, Y; Oncul, M; Akin, IM; Karabulut, AB; Gungor, S (2010)
Ultrasonographic Screening of Newborns for Congenital Anomalies of the

Tabel, Y; Haskologlu, ZS; Karakas, HM; Yakinci, C (2010)

Purpose: To search for the efficiency of scanning the newborns with routine urinary system ultrasonography.
Interleukin 8 gene 2767 A/G polymorphism is associated with increased

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 Schnolein purpura (HSP). A total of 115 ...
Clinical Features of Children With Henoch-Schonlein Purpura Risk Factors

Tabel, Y; Nano, FC; Dogan, DG; Elmas, AT (2012)

Introduction. This study aimed to evaluate renal involvement and factors affecting the prognosis in patients with Henoch-Schonlein purpura (HSP).
Effects of total parenteral nutrition on renal function in preterm

Tabel, Y; Oncul, M; Akin, IM; Karabulut, AB; Elmas, AT (2012)

Aim: The aim of this study was to establish serum sistatine C, urine beta(2) microglobulin, gluthatione-S -transferase pi and N-acetyle beta-D glucosaminidase levels in order to evaluate the effect of total parenteral ...

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