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Başlık için TIP, Radyoloji Anabilim Dalı, Makale Koleksiyonu listeleme

Başlık için TIP, Radyoloji Anabilim Dalı, Makale Koleksiyonu listeleme

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  • Evaluation of risk factors for arteriovenous fistula failure in patients undergoing hemodialysis 
    Sarı, Funda; Taşkapan, Hülya; Sığırcı, Ahmet; Akpınar, Beşir (Erciyes Med J, 2016)
    Objective: The aim of the present study is to evaluate the relationship between demographic characteristics, hematological and biochemical parameters, and elements of the coagulation system that may predispose a person ...
  • Examination of care burden of caregivers of oncology patients and the perceived social support form family 
    Çıtlık Sarıtaş, Seyhan; Kavak, Funda; Aksoy, Asude; Sarıtaş, Serdar (International Journal of Caring Sciences, 2017)
    Aim: This study was conducted to examine the care burden of caregiving family members of oncology patients and the perceived social support from family. Methods: The study was conducted as a descriptive and correlational ...
  • Examination of the antioxidant effects of pre-hsg melatonin use on ovarian surface epithelium inrats: an experimental study 
    Yilmaz, Esra Saygili; Sapmaz, Tansel; Kazgan, Halil; Yildiz, Sule Menziletoglu; Kocamaz, Derya; Akpolat, Nusret); Sapmaz, Ekrem (Wroclaw medıcal unıv, t chalubınskıego 6a, wroclaw, 50-368, poland, 2018)
    Background.There is no study of whether the dysplastic changes in the ovarian surface epithelium of X-ray-exposed rats during hysterosalpingography (HSG) decrease or not with the use of Lipiodol and melatonin given both ...
  • Fallot tetralojisinde aort çıkışlı sol pulmoner arter 
    Sığırcı, Ahmet; Yurdakul, M.; Tola, M.; Ölçer, T. (Türk Tanısal ve Girişimsel Radyoloji Dergisi, 1999)
  • Giant axonal neuropathy diffusion weighted imaging features of the brain 
    Alkan, Alpay; Sığırcı, Ahmet; Kutlu, Ramazan; Doğanay, Selim; Erdem, Gülnur; Yakıncı, Mehmet Cengiz (J Child Neurol, 2006)
    Giant axonal neuropathy is a rare autosomal recessive childhood disorder characterized by a peripheral neuropathy and features of central nervous system involvement. Magnetic resonance imaging (MRI) of an 11-year-old ...
  • Giant axonal neuropathy MRS findings 
    Alkan, Alpay; Kutlu, Ramazan; Sığırcı, Ahmet; Baysal, Tamer; Altınok, Tayfun; Yakıncı, Mehmet Cengiz (J Neuroimaging, 2003)
    Giant axonal neuropathy (GAN) is a rare genetic disease of childhood involving the central and peripheral nervous systems. Axonal loss with several giant axons filled with neurofilaments is the main histopathological feature ...
  • Glutaric aciduria type 1diagnosed after poliovirus immunization magnetic resonance findings 
    Alkan, Alpay; Baysal, Tamer; Yakıncı, Mehmet Cengiz; Sığırcı, Ahmet; Kutlu, Ramazan (Pediatr Neurol, 2002)
    Glutaric aciduria type I is an uncommon inborn error of metabolism. It is a serious disease, often with a fatal outcome. Magnetic resonance imaging findings and the clinical course of monozygotic twin females with ...
  • Hallermann streiff syndrome associated with complete agenesis of the corpus callosum 
    Sığırcı, Ahmet; Alkan, Alpay; Bıçak, Uğur; Yakıncı, Mehmet Cengiz (J Child Neurol, 2005)
    Hallermann-Streiff syndrome is a rare clinical entity with unknown etiology characterized by a birdlike face, microphthalmia, a beaked nose, hypotrichosis, and proportional small stature. We present a 4-year-old boy in ...
  • Hydatid disease with rare localizations a case report 
    Altınok, Tayfun; Kılıç, Süleyman; Sığırcı, Ahmet; Alkan, Alpay; Kutlu, Ramazan; Baysal, Tamer; Aydoğdu, İsmet (İnönü Üniversitesi Tıp Fakültesi Dergisi, 2002)
    Introduction: When the disease is in rare localization and especially has not a typical appearance of hydatid cyst, incorrect definitive diagnosis may be defined mistakenly, since the disease may be easily missed unless ...
  • Infantile sandhoff s disease multivoxel magnetic resonance spectroscopy findings 
    Alkan, Alpay; Kutlu, Ramazan; Yakıncı, Mehmet Cengiz; Sığırcı, Ahmet; Aslan, Mehmet; Saraç, Kaya (J Child Neurol, 2003)
    Sandhoff’s disease is a rare, genetic lysosomal storage disease leading to delayed myelination or demyelination. Although neuroimaging findings in this disease have been reported previously, magnetic resonance spectroscopy ...
  • Intratesticular arteriovenous malformation color doppler sonographic findings 
    Kutlu, Ramazan; Alkan, Alpay; Soylu, Ahmet; Sığırcı, Ahmet; Dusak, Abdurrahim (J Ultrasound Med, 2003)
    Arteriovenous malformations (AVMs) of male genitalia are rare. In the literature there are reports of AVMs involving the scrotum,1,2 penis,3 spermatic cord,4 testis, and epididymis5 and interventional treatment of scrotal ...
  • İnce barsak radyolojik inceleme yöntemleri 
    Sığırcı, Ahmet; Arda, Kemal (Güncel Gastroenteroloji, 1999)
  • Korpus kallozum disgenezisine eşlik eden beyin anomalileri ve klinik bulgular 
    Alkan, Alpay; Kutlu, Ramazan; Baysal, Tamer; Sığırcı, Ahmet; Altınok, Tayfun; Orkan, İsmet; Hallaç, Tarık; Saraç, Kaya (Tanısal ve Girişimsel Radyoloji Dergisi, 2003)
    Korpus kallozum disgenezisinin değişik formları ile eşlik eden beyin anomalileri ve klinik bulgular arasındaki ilişkinin araştırılması. GEREÇ VE YÖNTEM Kallozal disgenezisli 169 olgunun MRG bulguları retrospektif olarak ...
  • Kısmi sakrum agenezisi konvansiyonel radyografi ve üç boyutlu BT bulguları 
    Doğan, Metin; Sığırcı, Ahmet (Türk Tanısal ve Girişimsel Radyoloji Dergisi, 2002)
  • Letter on the article "A rare tumour of the neck in a child" 
    Dogan, M.; Kahraman, A. S.; Yildirim, I. O. (ELSEVIER MASSON, VIA PALEOCAPA 7, 20121 MILANO, ITALY, 2017)
  • Lower prevalence of non tumoral perfusion defects in left hepatic lobe during CT arterial portography with splenic artery injection 
    Kutlu, Ramazan; Akbulut, Ahmet; Sığırcı, Ahmet; Alkan, Alpay; Karaman, İbrahim; Baysal, Tamer; Saraç, Kaya (Eur J Radiol, 2004)
    Objective: To determine whether there is a difference in the prevalence of non-tumoral perfusion defects (NTPD) in left hepatic lobe during CT arterial portography (CTAP) through splenic (SA) and superior mesenteric artery ...
  • Management of non-vascular complications following renal transplantation using percutaneousapproach 
    Yildirim, Ismail Okan; Berktas, Bayram; Saglik, Semih; Piskin, Turgut; Dogan, Murat; Sahin, Idris; Taskapan, Hulya; Sarac, Kaya (Edızıonı luıgı pozzı, vıa panama 68, 00198 rome, ıtaly, 2018)
    OBJECTIVE: Non-vascular complications following renal transplantation can cause graft failure. In this study, we present our two-year experience with percutaneous treatment for non-vascular complications following renal ...
  • Melorheostosis of the left upper limp 
    Evren, Bahri; Çıkım Sertkaya, Ayşe; Köksal, İsmail; Kekilli, Ersoy (Open Journal of Medical Imaging, 2012)
    Melorheostosis, also known as Leri disease or flowing periosteal hyperostosis, is a rare, non-hereditary, benign, sklerosing bone dysplasia which radiologically characterized by the appearance of “melting wax flowing down ...
  • Merkezi Sinir Sistemi Enfeksiyonlarının Radyolojisi 
    Sığırcı, Ahmet (Turkiye Klinikleri J Neurosurg, 2016)
    Merkezi sinir sistemi (MSS) enfeksiyonları, akuttan kroniğe, sessiz halden yaşamı tehdit eden şekle doğru farklılık gösterebilir. Burada MSS enfeksiyonlarının tipik olabilecek özellikleri açıklanmaya çalışıldı. Bulgulardan ...
  • Merosin negative congenital muscular dystrophy diffusion weighted imaging findings of brain 
    Alkan, Alpay; Sığırcı, Ahmet; Kutlu, Ramazan; Aslan, Mehmet; Doğanay, Selim; Yakıncı, Mehmet Cengiz (J Child Neurol, 2007)
    Merosin-negative congenital muscular dystrophy is a rare genetic disease of childhood involving the central and peripheral nervous system. There were high signal intensities throughout the centrum semiovale, periventricular, ...