Yazar "Yildiran, Alisan" 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 ... -
A Case of Ataxia-telangiectasia Presented With Hemophagocytic Syndrome
Celiksoy, Mehmet H.; Cubuk, Pelin Ozyavuz; Guner, Sukru N.; Yildiran, Alisan (Lippincott Williams & Wilkins, 2018)Ataxia-telangiectasia (A-T) is a multisystem disease caused by a genetic defect located on the long arm of chromosome 11 (11p22-23). The gene defect results in the loss of A-T-mutated protein, subsequently leading to ... -
Comparison of Antifungal Susceptibilities in Candidemic Newborns According to Their Body Weights
Yildiran, Alisan; Belet, Nursen; Gunaydin, Murat; Kucukoduk, Sukru (Ekin Tibbi Yayincilik Ltd Sti-Ekin Medical Publ, 2010)Objectives: There is a lack of data comparing antifungal susceptibilities of Candida isolates in candidemic newborns weighing <= 1500 g versus those weighing >1500 g. This study aims to compare antifungal susceptibilities ... -
Could familial Mediterranean fever gene mutations be related to PFAPA syndrome?
Celiksoy, Mehmet H.; Ogur, Gonul; Yaman, Elif; Abur, Ummet; Fazla, Semanur; Sancak, Recep; Yildiran, Alisan (Wiley, 2016)BackgroundThe cause and pathophysiology of PFAPA syndrome is unknown. The aim of this study was to determine all MEFV gene variants relevant to familial Mediterranean fever in children with PFAPA syndrome. MethodsAll MEFV ... -
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. ... -
Early Diagnosis of Leucocyte Adhesion Molecule Deficiency Type 1
Guner, Sukru Nail; Sayar, Esra Hazar; Emiroglu, Melike; Borte, Stefan; Yildiran, Alisan; Reisli, Ismail (Springer/Plenum Publishers, 2014)… -
The Effect of Mode of Delivery on T Regulatory (Treg) Cells of Cord Blood
Yildiran, Alisan; Yurdakul, Engin; Guloglu, Deniz; Dogu, Figen; Arsan, Saadet; Arikan, Meltem; Ikinciogullari, Aydan (Springer India, 2011)To evaluate whether the mode of delivery (vaginal versus C-section) influences the levels of CD4+CD25+FOXP3+ Treg cells in cord blood and maternal peripheral blood and also to examine its relationship with plasma cortisol ... -
Effects of circulating endothelial progenitor cells, serum vascular endothelial growth factor and hypogammaglobulinemia in Perthes disease
Sezgin, Hicabi; Gulman, Birol; Cirakli, Alper; Bedir, Abdulkerim; Usta, Dilek; Coskun, Sina; Yildiran, Alisan (Turkish Assoc Orthopaedics Traumatology, 2014)Objective: The aim of this study was to investigate Legg-Calve-Perthes disease (PD) pathogenesis by comparing absolute circulating endothelial progenitor cell (EPC) counts, serum levels of vascular endothelial growth ... -
Hematopoietic Stem Cell Transplantation in Primary Immunodeficiency Patients in the Black Sea Region of Turkey
Yildiran, Alisan; Celiksoy, Mehmet Halil; Borte, Stephan; Guner, Sukru Nail; Elli, Murat; Fisgin, Tunc; Ogur, Gonul (Galenos Yayincilik, 2017)Hematopoietic stem cell transplantation is a promising curative therapy for many combined primary immunodeficiencies and phagocytic disorders. We retrospectively reviewed pediatric cases of patients diagnosed with primary ... -
Hemophagocytic Bone Marrow Aplasia With Plasma Cells in a RAG2-deficient SCID Case After a Nonconditioned Transplantation From a Fully Matched Sibling
Yildiran, Alisan; Fisgin, Tunc; Guner, Sukru N.; Kilic, Mehtap; Sancak, Recep; Ozyurek, Emel; Duru, Feride (Lippincott Williams & Wilkins, 2013)We report a RAG2-deficient patient with severe combined immunodeficiency and hemophagocytic bone marrow aplasia with plasma cells after a nonconditioned transplantation from a fully matched sibling. After engraftment, ... -
Immunoreconstitution in the First Thre Year After Hsct in A Newly Established Transplantation Unit
Yildiran, Alisan; Borte, Stephan; Elli, Murat; Fisgin, Tunc (Springer/Plenum Publishers, 2014)… -
Novel NLRP12 mutations associated with intestinal amyloidosis in a patient diagnosed with common variable immunodeficiency
Borte, Stephan; Celiksoy, Mehmet Halil; Menzel, Volker; Ozkaya, Ozan; Ozen, Fatma Zeynep; Hammarstroem, Lennart; Yildiran, Alisan (Academic Press Inc Elsevier Science, 2014)Heterozygous mutations in the NLRP12 gene have been found in patients with systemic auto-inflammatory diseases. However, the NLRP12-associated periodic fever syndromes show a wide clinical spectrum, including patients ... -
Pulmonary hypoplasia presenting with recurrent wheezing in an infant
Celiksoy, Mehmet Halil; Tander, Burak; Asilioglu, Nazik; Baris, Yakup Sancar; Yildiran, Alisan (Wiley, 2015)Pulmonary hypoplasia is characterized by decrease in the number and size of pulmonary airways, alveoli and vessels. In autopsy, pulmonary hypoplasia is a major cause of death in neonates and infants. The disease is usually ... -
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 ... -
Severe Hyper IgD Syndrome Associated with Heterozygote S52N Mevalonate Kinase Mutation
Celiksoy, Mehmet Halil; Berdeli, Afig; Comba, Atakan; Caltepe, Gonul; Yildiran, Alisan (Bilimsel Tip Yayinevi, 2017)Hyperimmunoglobulinemia D syndrome is a rare, autosomal recessively inherited autoinflammatory disease caused by mutations in the mevalonate kinase gene. The disease is characterized by clinically recurrent episodes of ... -
Unusual Clinical Presentation and Hemophagocytosis of Ataxia-Telangiectasia in Two Siblings With A Rare Mutation
Yildiran, Alisan; Celiksoy, M. Halil; Guner, S. Nail; Borte, Stephan (Springer/Plenum Publishers, 2014)… -
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 ...