Elif AZARSIZ

Tıp Fakültesi, Temel Tıp Bilimleri Bölümü, Tıbbi Biyokimya Anabilim Dalı

Research areas: Health Sciences, Medicine, Internal Medicine Sciences, Pediatric Immunology and Allergy, Child Health and Diseases, Biochemistry, Other, Fundamental Medical Sciences, Medical Genetics, Natural Sciences

Publications

• Exploring the association between interleukin-27 and Dermatophagoides-specific IgE responses in children with allergic rhinitis and asthma (2026)
• Elevated serum zonulin is associated with high attack frequency in hereditary angioedema: providing insight into the gut–angioedema axis (2026)
• Falsely elevated FSH levels due to assay interference: a case-based approach (2026)
• Staphylococcal enterotoxin-specific IgE Identifies a type-2 inflammatory endotype in chronic spontaneous urticaria (2026)
• Elevated serum zonulin is associated with high attack frequency in hereditary angioedema: providing insight into the gut-angioedema axis (2026)
• A comparative evaluation of salivary and serum procalcitonin to identify infants with serious bacterial infections (2026)
• Pre-Analytical Interference Causing Misleading hs-cTnT Elevation in a Pediatric Patient (2025)
• PULMONER ARTERİYEL HİPERTANSİYONDA YAVAŞ TEMPOLU SOLUNUMUN HASTA SONUÇLARINA ETKİSİ (2025)
• Falsely elevated FSH levels due to assay interference: a case-based approach (2025)
• The Role of Urinary Secretory Immunoglobulin A in the Pathophysiology of Interstitial Cystitis (2025)
• The Role of Soluble Urokinase Plasminogen Activator Receptor (suPAR) as an Early Indicator of Mortality in Pediatric Septic Shock (2024)
• Early Immunomodulatory Effects of Different Natural Surfactant Preparations in Preterms With Respiratory Distress (2022)
• Immunological changes during desensitization with cow’s milk: how differ from natural tolerance or nonallergic state? (2022)
• Mid-Regional Proadrenomedullin Levels in Primary Immunodeficiencies Complicated with Pulmonary Manifestations (2022)
• Eight years of follow-up experience in children with mendelian susceptibility to mycobacterial disease and review of the literature (2021)
• Eight years of follow-up experience in children with mendelian susceptibility to mycobacterial disease and review of the literature (2021)
• Eight years of follow-up experience in children with mendelian susceptibility to mycobacterial disease and review of the literature (2021)
• Autoantibody Positivity in Children with Chronic Diarrhea (2020)
• CSF levels of a set of neurotrophic factors (brain-derived neurotrophic factor, nerve growth factor) and neuropeptides (neuropeptide Y, galanin) in epileptic children. (2020)
• CSF levels of a set of neurotrophic factors (brain-derived neurotrophic factor, nerve growth factor) and neuropeptides (neuropeptide Y, galanin) in epileptic children (2020)
• Chronic granulamatous disease: Two decades of experience from a paediatric immunology unit in a country with high rate of consangineous marriages (2019)
• Ağır kombine ve kombine immün yetmezliklerde dirençli CMV enfeksiyonu: RAG1, ZAP70 ve ORAI1 mutasyonları (2019)
• Thymic output changes in children with clinical findings signaling a probable primary immunodeficiency. (2019)
• Ataksi-telenjiektazi tanılı hastaların retrospektif olarak incelenmesi: iki merkez deneyimi (2019)
• KRONİK İSHAL OLGULARINDA OTOANTİKOR POZİTİFLİĞİ (2019)
• Chronic granulomatous disease: Two decades of experience from a pediatric immunology unit in a country with high rate of consanguinity marriages (2019)
• Recurrent infections, neurologic signs, low serum uric acid levels, and lymphopenia in childhood: Purine nucleoside phosphorylase deficiency, an emergency for infants (2019)
• Kronik granülomatöz hastalık: moleküler patolojiler ve prognoza etkisi. (2018)
• CTLA-4 defekti: CVID tanısıyla izlenen hastaların moleküler patolojilerinden bir tanesi. (2018)
• Primer immün yetmezlik tanılı olgularda hedeflenmiş yeni nesil dizi analizi ile 264 gen mutasyon sonuçlarının değerlendirilmesi. (2018)
• Kök hücre nakli yapılan primer immün yetmezlik olgularının retrospektif değerlendirilmesi. (2018)
• A novel TTC37 mutation causing trichohepatoenteric syndrome in a patient with immunodeficiency without diarrhea (2018)
• Innate immunity chronic granulomatous disease: the prognostic effect of molecular pathologies (2018)
• X’e bağlı agammaglobülinemili olgularımızda moleküler analiz ve uzun süreli izlem sonuçlarımız ve erişkin yaşama geçiş (2018)
• Cerebrospinal Fluid Levels Of Neuropeptides In Children West Syndrome (2018)
• Relationship between immunological and microbiological structure of saliva according to the caries status in children. (2018)
• CSF Levels Of A Set Of Neuropeptides (BDNF, NGF, Neuropeptide Y and Galanin) in Children With Refractory Epilepsy (2018)
• Combined immunodeficiency due to ORAI1 mutation associated with refractory CMV infection, hypotonia and autoimmunity (2018)
• Prevalence of Coeliac Disease in Autoimmune Liver Disease and Primary Biliary Cholangitis (2018)
• <i>TNFRSF13B/TACI</i>Alterations in Turkish Patients with Common Variable Immunodeficiency and IgA Deficiency. (2018)
• Serum Amyloid A and Lipoprotein Associated Phospholipase A(2) Levels in Patients with Malign Melanoma: Correlations with Clinical Assessment and Stage (2018)
• Two male siblings with a novel LRBA mutation presenting with different findings of IPEX syndrome (2018)
• Familial inheritance and screening of first-degree relatives in common variable immunodeficiency and immunoglobulin A deficiency patients. (2018)
• Desensitization and tolerance in cow’xxs milk allergy (2017)
• Primer İmmün yetmezliklerde yeni nesil Dizileme Hedeflenmiş Gen yöntemi ile moleküler bozuklukların araştırılması (2017)
• X’ e bağlı immün yetmezlik-poliendokrinopati (IPEX) fenotipinde başvuran ve yeni tanımlanan LRBA defekti saptanan 2 kardeş olgu (2017)
• Desensitization and tolerance in cow's milk allergy (2017)
• FARKLI İMMÜNOLOJİK HASTALIKLARDA CD4CD45RACD31 NAİVE T HÜCRE DÜZEYLERİNİN DEĞERLENDİRİLMESİ (2017)
• GAIN-OF-FUNCTION (GOF) MUTATIONS IN SIGNAL TRANSDUCER AND ACTIVATOR OF TRANSCRIPTION 1 (STAT1): A CASE WITH CHRONIC MUCOCUTANEOUS CANDIDIASIS MIMICKING COMBINED IMMUNODEFICIENCY (2017)
• Desensitization and tolerance in cow’xxs milk allergy (2017)
• ROMATOLOJİK BULGULARLA BAŞVURAN HASTALARDA ANTİ BETA-2 GLİKOPROTEİN 1 POZİTİFLİĞİ (2017)
• Epileptik Ensefalopati Gösteren İnfantil spazmlı Çocuklarda Beyin Omurilik Sıvısında Nörotrofik Peptidlerin Düzeyleri (2017)
• A NOVEL MUTATION IN PIK3D CAUSING LATE ONSET COMBINED IMMUNODEFICIENCY (2017)
• A NOVEL MUTATION IN PIK3D CAUSING LATE ONSET COMBINED IMMUNODEFICIENCY (2017)
• Primer immün yetmezliklerde yeni nesil dizileme hedeflenmiş gen yöntemi ile moleküler bozuklukların araştırılması (2017)
• SUBKUTAN İMMÜNGLOBULİN TEDAVİSİ İLE İDEAL VE KORUYUCU DÜZEYLERDE SERUM IGG DÜZEYLERİ (2017)
• İnek sütü alerjisinde desensitizasyon ve tolerans (2017)
• PATHOGENIC GENETIC VARIANTS IDENTIFIED BY TARGETED NEXT-GENERATION SEQUENCING IN SOME UNDEFINED PRIMARY IMMUNODEFICIENCY CASES (IZMIR EXPERIENCE) (2017)
• ORAI1 MUTASYONUNA BAĞLI DİRENÇLİ CMV ENFEKSİYONU, HİPOTONİ VE OTOİMMÜNİTE İLE PREZENTE OLAN KOMBİNE İMMÜN YETMEZLİK OLGUSU (2017)
• X’E BAĞLI İMMÜN YETMEZLİK-POLİENDOKRİNOPATİ-ENTEROPATİ (IPEX) FENOTİPİNDE BAŞVURAN VE YENİ TANIMLANAN LRBA DEFEKTİ SAPTANAN İKİ KARDEŞ OLGU (2017)
• STAT-1 mutasyonu: Kombine immün yetmezlik kliniği ile seyreden Kronik Mukokutanöz kandidiyazis olgusu (2017)
• Gain-of-Function Mutations in STAT1: A Recently Defined Cause for Chronic Mucocutaneous Candidiasis Disease Mimicking Combined Immunodeficiencies (2017)
• Antı-β2 Glycoprotein I Antibodies in Children with Rheumatologic Disorders (2017)
• Diagnostic Accuracy of Interleukin-6, Interleukin-8, and Interleukin-10 for Predicting Bacteremia in Children with Febrile Neutropenia (2017)
• In vitro T lymphocyte proliferation by carboxyfluorescein diacetate succinimidyl ester method is helpful in diagnosing and managing primary immunodeficiencies (2017)
• Reference values for B-cell surface markers and co-receptors associated with primary immune deficiencies in healthy Turkish children (2017)
• Yaygın Değişken immün yetmezlikli çocuklarda kronik inflamasyon ve erken ateroskleroz belirteci olarak kitotriozidaz enzim aktivitesi (2016)
• B CELL CO RECEPTORS CD19 CD21 81 AND SURFACE MARKERS CD20 CD22 CD27 IN UNCLASSIFIED HYPOGAMMAGLOBULINEMIA PATIENTS (2016)
• Pathogenic genetic variants identified by targeted next-generation sequencing in some undefined primary immunodeficiency cases (İzmir Experience) (2016)
• İnek sütü alerjisinde desensitizasyon ve tolerans (2016)
• CD19, CD20, CD21, CD22, CD27 and CD81 values in healthy Turkish children. (2016)
• B cell co-receptors (CD19, CD21, CD81) and surface markers (CD20, CD22, CD27) in unclassified hypogammaglobulinemia patients (2016)
• Nedeni saptanamayan hipogammaglobulinemi ayırıcı tanısında B hücre koreseptörleri CD19 Cd20 Cd21 CD22 CD27 CD81 (2016)
• Spesifik primer immun yetmezlik olgularında CFSE metodu ile in-vitro T lenfosit proliferasyon yanıtlarına laboratuvar yaklaşım (2016)
• The effect of periodontal treatment on GCF LL 37 levels in periodontal destruction (2016)
• Does smoking affect gingival crevicular fluid LL-37 levels following non-surgical periodontal treatment in chronic periodontitis? (2016)
• Chitotriosidase enzyme activity: is this a possible chronic inflammation marker in children with common variable immunodeficiency and early atherosclerosis? (2016)
• Clinical, Laboratory and Molecular Approach to Ten Children with Congenital Neutropenia (2016)
• Yaygın değişken immün yetmezlikli çocuklarda kronik inflamasyon ve erken ateroskleroz belirteci olarak kitotriosidaz enzim aktivitesi (2016)
• Lipoprotein-associated phospholipase A₂: a new marker to determine cardiovascular risk in hypercholesterolemic dyslipidaemic children. (2016)
• Recombinase Activating Gene 1 Deficiencies Without Omenn Syndrome May Also Present With Eosinophilia and Bone Marrow Fibrosis. (2016)
• A clinical and laboratory approach to the evaluation of innate immunity in pediatric CVID patients (2015)
• CVID ve doğal immünite nötrofil göçü ve fagoburst aktivitesi adezyon molekülleri CD11a CD18 NK hücre fonksiyonları ve NKT hücreler (2015)
• CD4 CD25 FOXP3 T regulatory cells Th1 CCR5 IL 2 IFN and Th2 CCR4 IL 4 IL 13 type chemokine receptors and intracellular cytokines in children with commonvariable immunodeficiency (2015)
• Nötrofil göçü ve fagoburst aktivitesi adezyon molekülleri CD11a CD18 NK hücre fonksiyonları ve NKT hücreler (2015)
• Early immunomodulatory effects of different natural surfactant preparations in preterm infants with respiratory distress syndrome (2015)
• Does smoking affect gingival crevicular fluid LL 37 levels in chronic periodontitis patients following non surgical periodontal treatment (2015)
• CVID ve doğal immünite: nötrofil göçü ve oksidatif burst aktivitesi, adezyon molekülleri (CD11a, CD18), NK hücre fonksiyonları ve NKT hücreler (2015)
• Early immunomodulatory effects of different natural surfactant preparations in preterm infants with respiratory distress syndrome P 18 syf 35 (2015)
• A clinical and laboratory approach to the evaluation of innate immunity in pediatric cvid patients (2015)
• Yaygın değişken immün yetmezlikli çocuklarda CD4 CD25 Foxp3 T regulatuar hücreler Th1 CCR5 IL2 IFN g ve Th2 CCR4 IL4 IL13 tip kemokin reseptörleri ve hücre içi sitokinleri (2015)
• Malign melanomlu hastalarda serum amiloid A ve lipoprotein ilişkili fosfolipaz A2 düzeylerinin aaştırılması ve klinik önemi (2015)
• Interleukin-1 receptor antagonist deficiency with a novel mutation, late onset and a successful treatment with canakinumab (2015)
• Malign melanomlu hastalarda serum amiloid A ve Lipoprotein ilişkili fosfolipaz A2 düzeylerinin araştırılması ve klinik önemi (2015)
• Diverse clinical phenotypes in recombinase activating gene 1 deficiency a single center experience (2015)
• Fcγ receptor polymorphisms in patients with transient hypogammaglobulinemia of infancy presenting mild and severe infections (2015)
• Interleukin 1 receptor antagonist deficiency with a novel mutation late onset and a successful treatment with canakinumab a case report (2015)
• Does smoking affect gingival crevicular fluid LL 37 levels in patients with chronic periodontitis following non surgical periodontal treatment Abs no P0127 (2015)
• Yaygın değişken immün yetmezlikli çocuklarda CD4+CD25+FOXP3+ T regulatuvar hücreler, Th1 (CCR5, IL-2, IFN-?) ve Th2 (CCR4, IL-4, IL-13) tip kemokin reseptörleri ve hücre içi sitokinleri (2015)
• CD4(+)CD25(+)Foxp3(+) T regulatory cells, Th1 (CCR5, IL-2, IFN-gamma) and Th2 (CCR4, IL-4, IL-13) type chemokine receptors and intracellular cytokines in children with common variable immunodeficiency (2015)

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