DSpace@İnönü

Yazar "Tabel, Y" için listeleme

Yazar "Tabel, Y" için listeleme

Sırala: Sıra: Sonuçlar:

  • 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 ...
  • 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 ...
  • 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 ...
  • 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 ...
  • 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 ...
  • 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 ...
  • 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 ...
  • 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 ...
  • 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.
  • 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 ...
  • 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 ...
  • 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 ...
  • 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 ...
  • 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, ...
  • 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 ...
  • 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.
  • 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 ...
  • 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, ...
  • 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 ...
  • 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 ...