Yazar "Kutlug, Seyhan" için listeleme
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A Case of Acute Generalised Exanthematous Pustulosis Induced by Paracetamol
Kutlug, Seyhan; Celiksoy, Mehmet Halil; Eroglu, Betul; Yildiz, Levent; Yildiran, Alisan (Bilimsel Tip Yayinevi, 2017)Acute generalized exanthematous pustulosis is an exanthematous disease characterized by a great number of pustules on an acutely erythematous and edematous surface on the skin. These pustules are smaller than 5 mm, have ... -
Development of multiple gallstones in a child with lipopolysaccharide-responsive beige-like anchor protein mutation
Kutlug, Seyhan; Boztug, Kaan; Yildiran, Alisan (Termedia Publishing House Ltd, 2019)A defect in the lipopolysaccharide-responsive beige-like anchor protein (LRBA) gene is a newly defined rare cause of primary immunodeficiency diseases, which manifests as immune dysregulation and humoral immune deficiency. ... -
Evaluation of olfactory function in children with allergic rhinitis and nonallergic rhinitis
Kutlug, Seyhan; Gunbey, Emre; Sogut, Ayhan; Celiksoy, Mehmet Halil; Kardas, Semsettin; Yildirim, Ugur; Sancak, Recep (Elsevier Ireland Ltd, 2016)Objectives: Allergic rhinitis (AR) occurs when the symptoms of rhinitis arise as a result of allergen induced nasal mucosal inflammation. In the presence of rhinitis symptoms without infection or an allergic reaction in ... -
Mean Platelet Volume in Children with Chronic Spontaneous Urticaria
Kutlug, Seyhan; Sogut, Ayhan; Celiksoy, Mehmet Halil; Paksu, Muhammet Sukru; Guner, Sukru Nail; Murat, Naci; Sancak, Recep (Bilimsel Tip Yayinevi, 2017)Objective: It has been suggested that mean platelet volume can be used as a marker of inflammation in some inflammatory diseases. This marker has not been investigated adequately in children with allergic disease. The aim ... -
Seven chronic granulomatous disease cases in a single-center experience and a review of the literature
Kutlug, Seyhan; Sensoy, Gulnar; Birinci, Asuman; Saraymen, Berkay; Koker, Mustafa Yavuz; Yildiran, Alisan (Allergy Immunol Soc Thailand,, 2018)Background: Chronic granuloniatous disease (CGD) is a rare primary immunodeficiency caused by defects in the nicotinamide adenine dinucleotide phosphate (NADPH) oxidase enzyme system. this disease causes the disordered ... -
Vesicourethral Reflux-Induced Renal Failure in a Patient with ICF Syndrome Due to a Novel DNMT3B Mutation
Kutlug, Seyhan; Ogur, Gonul; Yilmaz, Aysegul; Thijssen, Peter E.; Abur, Ummet; Yildiran, Alisan (Wiley, 2016)ICF syndrome is a primary immunodeficiency disease characterized by hypo-or agammaglobulinemia, centromeric instability mainly on chromosomes 1, 9, and 16 and facial anomalies. ICF syndrome presents with frequent respiratory ...