Yazar "Misirlioglu, Emine Dibek" için listeleme
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Clinical and etiologic evaluation of the children with chronic urticaria
Azkur, Dilek; Civelek, Ersoy; Toyran, Muge; Misirlioglu, Emine Dibek; Erkocoglu, Mustafa; Kaya, Aysenur; Kocabas, Can Naci (Ocean Side Publications Inc, 2016)Background: Chronic urticaria (CU) is a skin disorder defined as daily or almost daily exhibition of pruritic and transient wheals that last for >6 weeks. CU is divided into two subtypes: chronic spontaneous urticaria (CSU) ... -
Do cerebral blood flow velocities change in iron deficiency anemia?
Aliefendioglu, Didem; Yilmaz, Sevda; Misirlioglu, Emine Dibek; Saygi, Semra; Ozdogan, Selver; Kocak, Ulker (Lippincott Williams & Wilkins, 2007)Infants with iron deficiency had lower scores when tested for mental and motor development than their peers with better iron status. The aim of this study was to examine cerebral blood flow velocity in infants with iron ... -
Helicobacter pylori infection in mother and infant pairs in Anatolia
Hizel, Selda; Ozden, Ali; Tanzer, Fatos; Kisa, Ucler; Misirlioglu, Emine Dibek; Buyukkayhan, Derya; Kisa, Ozgul (Aves, 2010)Background/aims: The aim of this prospective study was to determine the seroprevalence rates of Helicobacter pylori in mother and infant pairs and to discuss the possible fecal-oral transmission route of Helicobacter pylori ... -
Remembering the Importance of an Old Friend: History Taking in Preoperative Evaluation of Healthy Children: A Single Center Experience
Toprak, Sule; Kocak, Ulker; Misirlioglu, Emine Dibek; Sanli, Cihat; Albayrak, Meryem; Basar, Hulya (Gazi Univ, Fac Med, 2016)Objective: To investigate the consequences of routine laboratory tests that lead to surgical delay or high cost in patients with a normal medical history and physical examination who undergo minor surgical interventions. ... -
The spectrum of FMF mutations and genotypes in the referrals to molecular genetic laboratory at KÄaut +/- rÄaut +/- kkale University in Turkey
Gunel-Ozcan, Aysen; Sayin, Derya Beyza; Misirlioglu, Emine Dibek; Guliter, Sefa; Yakaryilmaz, Fahri; Ensari, Cuneyt (Springer, 2009)Familial Mediterranean Fever (FMF) is an autosomal recessive genetic disorder characterised by recurrent and self-limited abdominal pain, synovitis and pleuritis. MEFV gene mutations are responsible from the disease and ...