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Yayın tarihi için Çocuk Sağlığı ve Hastalıkları Anabilim Dalı listeleme

Yayın tarihi için Çocuk Sağlığı ve Hastalıkları Anabilim Dalı listeleme

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  • Altuntaş, Buket; Erden, Ayşe; Karakurt, Cemşit; Kut, Altuğ; Senbil, Nesrin; Yurdakul, Mehmet (Journal Of Clınıcal Ultrasound, 1998)
    A 13-year-old girl was referred for assess-ment of severe gastrointestinal tract bleeding. Herliver function tests were normal, and she had no evi-dence of chronic liver disease or history of significanttrauma. Clinical ...
  • Altuntaş, Buket; Erden, Ayşe; Karakurt, Cemşit; Kut, Altuğ; Şenbil, Nesrin; Yurdakul, Mehmet (Journal of clinical ultrasound, 1998)
    A 13-year-old girl was referred for assessment of severe gastrointestinal tract bleeding. Her liver function tests were normal, and she had no evidence of chronic liver disease or history of significant trauma. Clinical ...
  • Kuyucu, Necdet; Karakurt, Cemşit; Bilaloğlu, Eris; Karacan, Candemir; Teziç, Tahsin (J tropical ped, 1999)
  • Kuyucu, Necdet; Karakurt, Cemşit; Bilaloğlu, E.; Teziç, Tahsin (J Trop Pediatr. 1999 Aug;45(4):245-7., 1999)
    The diagnostic value of serum adenosine deaminase (ADA) activity was evaluated in childhood pulmonary tuberculosis. Serum ADA levels were measured in 20 children diagnosed with pulmonary tuberculosis (group 1) and 150 ...
  • Karakurt, Cemşit; Sipahi, T.; Ceylaner, S.; Şenocak, Filiz; Karademir, Selmin; Becer, M. (Clinical Pediatrics, 2001)
    Cardiac examination revealed apical midsystolic click and 2/6 systolic murmur. Radiographic examination of the chest and gastrointestinal system and abdominal ultrasonography appeared normal. Echocardiography ...
  • 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 ...
  • 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 ...
  • Karakurt, Cemşit; Sipahi, T.; Ceylaner, S.; Şenocak, Filiz; Karademir, Selmin; Becer, M. (Clinical Pediatrics, 2001)
    Congenital cutis laxa is a rare inherited disorder of connective tissue manifested by loose, hanging skin. Cutis laxa may be inherited (autosomal dominant, autosomal recessive) or acquired. As opposed to the recessive ...
  • Karademir, Selmin; Oğuz, Deniz; Şenocak, Filiz; Öcal, Burhan; Karakurt, Cemşit; Çabuk, Feryal (Pediatrics International, 2003)
    Background : The arthritis of rheumatic fever is very responsive to treatment with salicylates, but there aremany adverse reactions, especially hepatotoxicity, due to aspirin (acetylsalicylic acid) therapy. These ...
  • Karademir, Selmin; Oğuz, Deniz; Şenocak, Filiz; Öcal, Burhan; Karakurt, Cemşit; Çabuk, Feryal (Pediatrics International, 2003)
    Background: The arthritis of rheumatic fever is very responsive to treatment with salicylates, but there are many adverse reactions, especially hepatotoxicity, due to aspirin (acetylsalicylic acid) therapy. These ...
  • Saraç, Kaya; Akıncı, Ayşehan; Alkan, Alpay; Aslan, Mehmet; Baysal, Tamer; Özcan, Abdulcemal (NEURORADIOLOGY, 2005)
    The metabolite changes in the brains of children with poorly controlled type 1 diabetes mellitus (DM) were investigated by proton magnetic resonance spectroscopy (MRS). A total of 30 subjects and 14 age-matched healthy ...
  • Çeliker, Alpay; Karakurt, Cemşit (Turk J Pediatr. 2005 Oct-Dec;47(4):323-6., 2005)
    Transcatheter closure of atrial septal defect (ASD) has been used as an alternative to open heart surgery. Although transcatheter closure of ASD with the Amplatzer septal occluder is a safe and feasible method in pediatric ...
  • Karakurt, Cemşit; Oğuz, Deniz; Karademir, Selmin; Sungur, Metin; Öcal, Burhan (Echocardiography, 2006)
    A congenital partial defect of the right-sided pericardium is a rare cardiac anomaly and it represents defective formation of the pleuropericardial membrane. Patients can be asymptomatic, but they may experience chest ...
  • Çeliker, Alpay; Karakurt, Cemşit; Karagöz, Tevfik (Acta Cardiologica, 2006)
    The dual-chamber pacing systems allow for AV synchrony, but generally require the placement of two separate transvenous leads. Single-lead atrioventricular synchronous pacing system (VDD) using single-pass leads has been ...
  • Çeliker, Alpay; Karakurt, Cemşit; Karagöz, Tevfik (Acta Cardiologica, 2006)
    The dual-chamber pacing systems allow for AV synchrony, but generally require the placement of two separate transvenous leads. Single-lead atrioventricular synchronous pacing system (VDD) using single-pass leads has been ...
  • Karakurt, Cemşit; Deniz, Oğuz; Karademir, Selmin; Sungur, Metin; Öcal, Burhan (Echocardiography, 2006)
    congenital partial defect of the right-sided pericardium is a rare cardiac anomaly and it representsdefective formation of the pleuropericardial membrane. Patients can be asymptomatic, but they mayexperience chest pain, ...
  • 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 ...
  • Karakurt, Cemşit; Selimoğlu, Ayşe; Özen, Metehan; Koçak, Gülemdam (Anadolu Kardiyol Derg 2007; 7: 459-62., 2007)
    A 48-year-old man who was admitted to hospital because of syncope, transient ischemic attack, palpitations and chest pain. On physical examination, he had sight deficiency on the right eye. Electrocardiography revealed ...
  • 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 ...
  • 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 ...