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Başlık için TIP, Çocuk Sağlığı ve Hastalıkları Anabilim Dalı, Makale Koleksiyonu listeleme

Başlık için TIP, Çocuk Sağlığı ve Hastalıkları Anabilim Dalı, Makale Koleksiyonu listeleme

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  • Is edema in minimal change disease of childhood really hypovolemic 
    Tabel, Yılmaz; Mungan, İlke; Karakurt, Cemşit; Koçak, Gülendam; Güngör, Serdal (Int Urol Nephrol, 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 ...
  • Is edema in minimal change disease of childhood really hypovolemic 
    Tabel, Yılmaz; Mungan, İlke; Karakurt, Cemşit; Koçak, Gülemdar; Güngör, Serdal (Int Urol Nephrol, 0–0., 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 ...
  • Kawasaki disease: evaluation of 15 cases 
    İnce, Damla; Elkıran, Özlem; Karakurt, Cemşit; Tabel, Yılmaz (Journal of Turgut Ozal Medical Center, 2016)
    Kawasaki disease is characterized with acute systemic self–limited vasculitis, commonly affects middle and small size arteries, occurs predominantly in children under 5 years old age. Most common causes of morbidity and ...
  • Nasotracheal ıntubation in children for outpatient dental surgery: Is fiberoptic bronchoscopy useful 
    Özkan, Ahmet Selim; Akbaş, S. (MEDKNOW PUBLICATIONS & MEDIA PVT LTD, B-9, KANARA BUSINESS CENTRE, OFF LINK RD, GHAKTOPAR-E, MUMBAI, 400075, INDIA, 2018)
    Background: The aim of our study was to compare the hemodynamic responses and adverse events associated with nasotracheal intubation (NTI) using a fiberoptic bronchoscope (FOB) and a direct laryngoscope (DLS) in children ...
  • Neuroimaging Findings in Hyperargininemia 
    Güngör, Serdal; Akıncı, Ayşehan; Fırat, Ahmet Kemal; Tabel, Yılmaz; Alkan, Alper (Journal of Neuroimaging, 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 ...
  • Neuroimaging findings in hyperargininemia 
    Güngör, Serdal; Akıncı, Ayşehan; Fırat, Ahmet Kemal; Tabel, Yılmaz; Alkan, Alpay (Journal of Neuroimaging, 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 ...
  • Pediatric wilson's disease: findings in different presentations. A cross-sectional study 
    Gungor, Sukru; Selimoglu, Mukadder Ayse; Varol, Fatma Ilknur; Gungor, Serdal (Assocıacao paulısta medıcına, av brıg luıs antonıo, 278-7 andar, sao paulo, cep01318-901, brazıl, 2018)
    BACKGROUND: Wilson's disease (WD) may present with different manifestations: from an asymptomatic state to liver cirrhosis. Here, we aimed to evaluate clinical presentations and laboratory findings and prognoses among WD ...
  • Perioperative managaement of leavoarial cardianal vein in the absence of the brachiocephalic vein 
    Dişli, Olcay Murat; Battaloğlu, Bektaş; Erdil, Nevzat; Karakurt, Cemşit; Elkıran, Özlem (Tex Heart Ins J, 2013)
    Levoatrial cardinal vein is a rare congenital anomaly of the systemic veins. It is commonly associated with left-sided obstructive conditions such as aortic atresia, mitral atresia, and cor triatriatum. We report the ...
  • Plasma endothelin 1 and nitrate levels in Down s syndrome with complete atrioventricular septal defect associated pulmonary hypertension a comparison with non Down s syndrome children 
    Sungur, Metin; Öcal, Burhan; Oğuz, Deniz; Karademir, Selmin; Karakurt, Cemşit; Şenocak, Filiz (Eur J Pediatr (2009) 168:593–597., 2009)
    Children with Down’s syndrome (DS)-associated complete atrioventricular septal defect (AVSD) have rapid and aggressive development of pulmonary vascular disease when compared with non-Down’s syndrome (ND) children. ...
  • Plasma endothelin 1 and nitrate levels in Down s syndrome with complete atrioventricular septal defect associated pulmonary hypertension a comparison with non Down s syndrome children 
    Sungur, Metin; Öcal, Burhan; Oğuz, Deniz; Karademir, Selmin; Karakurt, Cemşit; Şenocak, Filiz (European Journal of Pediatrics, 2009)
    Abstract Children with Down’s syndrome (DS)-associated complete atrioventricular septal defect (AVSD) have rapid and aggressive development of pulmonary vascular disease when compared with non-Down’s syndrome (ND) ...
  • Plasma kisspeptin levels in girls with premature thelarche 
    Akıncı, Ayşehan; Çetin, Dilek; İlhan, Nevin (J Clin Res Pediatr Endocrinol, 2012)
    Ob jec ti ve: Premature thelarche (PT) is defined as isolated breast development without secondary sex characteristics in girls below the age of eight. We aimed to determine whether the level of kisspeptin, which plays ...
  • Plasma kisspeptin levels in girls with premature thelarche 
    Akıncı, Ayşehan; Çetin, Dilek; İlhan, Nevin (J Clin Res Pediatr Endocrinol, 2012)
    Gonadotropin-releasing hormone analog (GnRHa) therapy is used in idiopathic central precocious puberty (ICPP) worldwide. It has also been shown that during this therapy, body mass index (BMI) increases slightly as a side ...
  • Possible association between fluconazole administration and acute hyperkalemia in a critically ill cyanotic infant 
    Elkıran, Özlem; Karakurt, Cemşit; Koçak, Gülemdar; Tabel, Yılmaz; Güngör, Serdal (Arch Med Sci, 2015)
    Fluconazole, an azole antifungal agent, inhibits the fungal cytochrome P450 enzyme. Although in vitro data show that fluconazole is not a potent inhibitor of mammalian P450 enzymes, hyperkalemia secondary to adrenal ...
  • Prenatal diagnosis of a patient with tetralogy of fallot and an absent pulmonary valve 
    Karakurt, Cemşit; Koçak, Gülendam; Elkıran, Özlem (Pediatric Cardiology, 2011)
    A 34-week-gestation fetus of a gravid 3 mother 29 years of age was referred to our hospital due to an abnormal vascular image on obstetric ultrasonographic examination. The family history of congenital heart disease was ...
  • Presence of a D8 17 B lymphocyte marker and HLA DR subgroups in patients with rheumatic heart disease 
    Karakurt, Cemşit; Celiloğlu, Can; Özgen, Ünsal; Yeşilada, Elif; Yoloğlu, Saim; Zabriskie, John; Koçak, Gülendam (Anadolu Kardiyol Derg 2011; 11: 314-8., 2011)
    Objective: The aim of our study was to investigate the association of HLA antigens and a non-HLA protein D8/17 with rheumatic heart disease and its pattern of cardiac involvement. Methods: This cross- sectional observational ...
  • Prevalance and outcome of congenital heart disease in patients with neural tube defect 
    Koçak, Gülendam; Önal, Selami Çağatay; Karakurt, Cemşit; Ateş, Özkan; Çaylı, Süleyman; Yoloğlu, Saim (J Child Neurol, 2008)
    A prospective clinical study was designed to establish the risk factors, the prevalence, and the progress of congenital heart defects in children with neural tube defects. Study included 90 children with a mean age of ...
  • Prevalance and outcome of congenital heart disease in patients with neural tube defect 
    Koçak, Gülemdar; Önal, Çağatay; Koçak, Ayhan; Karakurt, Cemşit; Ateş, Özkan; Çaylı, Süleyman R.; Yoloğlu, Saim (Child Neurol, 0–0., 2008)
    A prospective clinical study was designed to establish the risk factors, the prevalence, and the progress of congenital heart defects in children with neural tube defects. Study included 90 children with a mean age of ...
  • Prognostic value of hart rate turbulence and heart rate variability in children with dilated cardiomyopathy 
    Karakurt, Cemşit; Aytemir, Kudret; Karademir, Selmin; Sungur, Metin; Oğuz, Deniz; Öcal, Burhan; Şenocak, Filiz (Acta Cardiologica, 2007)
    The aim of our study is to evaluate the prognostic value of heart rate turbulence and heart rate variability in children with dilated cardiomyopathy (DCM). Twenty-five children with DCM and 24 age- and sex-matched healthy ...
  • Pseudoachondroplasia in a child with prolapse of the mitral valve 
    Karakurt, Cemşit; Karademir, Selmin; Üner, Çiğdem (Cardiology in the Young, 2001)
    Pseudoachondroplasia is an autosomal dominant variant of osteochondroplasia that results in mild to severe short-limb dwarfism and early-onset of osteoarthrosis. It has been linked to results from mutations in the gene ...
  • Pseudoachondroplasia in a child with prolapse of the mitral valve 
    Karakurt, Cemşit; Karademir, Selmin; Üner, Çiğdem (Cardiol Young 2001; 11: 559–56., 2001)
    t Pseudoachondroplasia is an autosomal dominant variant of osteochondroplasia that results in mild to severe short-limb dwarfism and early-onset of osteoarthrosis. It has been linked to results from mutations in the gene ...