Afig BERDELİ
Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Çocuk Sağlığı Ve Hastalıkları Anabilim Dalı
Araştırma alanları: Sağlık Bilimleri, Tıp, Dahili Tıp Bilimleri, İç Hastalıkları, Çocuk Sağlığı ve Hastalıkları, Nefroloji, Tıbbi Genetik, Yaşam Bilimleri, Temel Bilimler, Diş Hekimliği
Yayınlar
- Podocyte dysfunction in kidney diseases: Mechanisms and therapeutic advances (2026)
- Stem cells: Definition, characteristics, classification, sources and ethical approaches (2026)
- Stem cells: Definition, characteristics, classification, sources and ethical approaches (2026)
- Exploring the role of NOD2 variants in pediatric undifferentiated recurrent fever: a clinical and functional perspective (2025)
- Exploring the role of NOD2 variants in pediatric undifferentiated recurrent fever: a clinical and functional perspective (2025)
- Distribution and classifications of PKHD1 gene variants in Turkish population with next generation sequencing method (2024)
- MAPK pathway and NIS in B-CPAP human papillary thyroid carcinoma cells treated with resveratrol (2024)
- Yeni Nesil Dizileme Kullanılarak NLRC4 Gen Varyantlarının Dağılımının Değerlendirilmesi (2024)
- Retrospective evaluation of the short-term effectiveness of non-enzymatically isolated stromal vascular fraction cells in patients with knee osteoarthritis (2024)
- MAPK pathway and NIS in B-CPAP human papillary thyroid carcinoma cells treated with resveratrol (2024)
- Analysis of IL-1β, TGF-β, IL-5, ACE, PTPN22 gene polymorphisms, and gene expression levels in Turkish children with IgA vasculitis (2024)
- Analysis of IL-1β, TGF-β, IL-5, ACE, PTPN22 gene polymorphisms, and gene expression levels in Turkish children with IgA vasculitis (2023)
- PKHD1 Gen Varyantlarının Yeni Nesil Dizileme Yöntemi İle Dağılımı Ve Sınıflandırılması (2023)
- Long-Term Outcomes of Patients with Atypical Hemolytic Uremic Syndrome (2023)
- Analysis of IL-1β, TGF- Β, Il-5, ACE and PTPN22 Gene Polymorphisms and GEN Expression Levels in Turkish Chlidren with IgA Vasculitis (2023)
- MEFV gene allele frequency and genotype distribution in 3230 patients’ analyses by next generation sequencing methods (2022)
- Next-Generation Sequencing Analysis of MVK, NLRP3, TNFRSF1A, and PSTPIP1 Genes in Patients without MEFV Gene Variation and Genotype–Phenotype Correlation (2022)
- Long-term follow-up of alkaptonuria patients: Single center experience (2022)
- Next-Generation Sequencing Analysis of MVK, NLRP3, TNFRSF1A, and PSTPIP1 Genes in Patients without MEFV Gene Variation and Genotype–Phenotype Correlation (2022)
- Investigation of neuraminidase 1 gene association in Henoch-Schönlein Purpura (HSP) with renal involvement (2022)
- Screening of OTULIN gene mutation with targeted next generation sequencing in Turkish populations and in silico analysis of these mutations (2022)
- Effects of 15-lipoxygenase overexpressing adipose tissue mesenchymal stem cells on the Th17 / Treg plasticity (2022)
- Four diseases, PLAID, APLAID, FCAS3 and CVID and one gene (PHOSPHOLIPASE C, GAMMA-2; PLCG2): Striking clinical phenotypic overlap and difference (2021)
- Blockade of PD-1/PD-L1 Axis May Improve NK-92 Cell Inhibition Caused by Mesenchymal Stem Cells (2021)
- OTULIN Gen Varyantlarının Yeni Nesil Dizileme Kullanılarak Değerlendirilmesi ve Bu Varyantların in silico Analizleri (2021)
- Effects of 15-lipoxygenase overexpressing adipose tissue mesenchymal stem cells on the Th17 / Treg plasticity (2021)
- Inflamazomlar (2021)
- Yeni Nesil Dizileme Kullanılarak 3230 Bireyde Tespit Edilen MEFV Varyantlarının Allel Frekansları ve Genotip Dağılımlarının Analizi (2021)
- Genetik Otoinflamatuar Hastalıklar Tanı Yöntemleri ve Tedavilerinde Yenilikler (2021)
- Ubikitinasyon Bozukluk Hastalıkları (2021)
- Four diseases, PLAID, APLAID, FCAS3 and CVID and one gene (PHOSPHOLIPASE C, GAMMA-2; PLCG2 ): striking clinical phenotypic overlap and difference (2021)
- Ailesel Akdeniz Ateşi-Pryrin İlişkili Hastalık (2021)
- Four diseases, PLAID, APLAID, FCAS3 and CVID and one gene (PHOSPHOLIPASE C, GAMMA‐2; PLCG2): Striking clinical phenotypic overlap and difference (2021)
- PRIMARY HYPEROXALURIA TYPE 1 PROGRESSING TO END-STAGE RENAL FAILURE AT INFANCY (2021)
- A rare cause of urolithiasis in an infant: Questions (2021)
- MYH9-related Disease Caused by an R1165C Mutation in a Child With Previous Diagnosis of Immune Thrombocytopenic Purpura (2021)
- A rare cause of urolithiasis in an infant: Answers (2021)
- Demographic and clinical characteristics of children with autosomal dominant polycystic kidney disease: a single center experience (2021)
- NLRP3 GENE MUTATION IN A PATIENT WITH RECURRENT APHTHOUS LESIONS (2020)
- NPHS2 Gene Mutations in Azerbaijani Children with Steroid-Resistant Nephrotic Syndrome (2020)
- Inflammasomes and their regulation in periodontal disease: A review (2020)
- Blau Syndrome and Early-Onset Sarcoidosis: A Six Case Series and Review of the Literature (2020)
- Typical Rett syndrome in a young boy with hemizygous c.316CT mutation in MECP2 gene (2020)
- The effects of mesenchymal stem cells on the IDO, HLA-G and PD-L1 expression of breast tumor cells MDA-MB-231 and MCF-7 (2019)
- A new KCNQ2 mutation and clinical findings (2019)
- Nefrotik Düzeyde Proteinüri Ve Fokal Segmental Glomerüloskleroz Saptanan Dent Hastalığı Olgusu (2019)
- Genetics and outcome of atypical hemolytic-uremic syndrome in Turkish children: a retrospective study between 2010 and 2017, a single-center experience. (2019)
- Atipik Hemolitik Üremik Sendrom ve Pauci-immun Kresentrik Glomerulonefrit : Nadir Birliktelik (2019)
- Genetics and Consequences of Atypical Hemolytic-uremic Syndrome in Turkish Children (2019)
- NPHS2 gene sequencing results in children of the Azerbaijani population with different types of nephrotic syndrome caused by chronic glomerulonephritis. (2019)
- Genotypic and Phenotypic Features of Both NPHS1 and NPHS2 Genes in Infantile Nephrotic Syndrome and Prognostic Effect of E117K Polymorphism in NPHS1 Gene (2019)
- Treatment of familial mediterranean fever with canakinumab in patients who are unresponsive to colchicine (2019)
- Kompleman İlişkili aHUS Olgu Serisi: Klinik Özellikler, Tedavi ve Gözlem Sonuçları: (2019)
- Glomerüler Elektron Mikroskopi Bulgularının Atipik Hemolitik Üremik Sendrom Tanısındaki Önemi (2019)
- Distribution of nucleotide variants in the DNA sequence of ERCC1 and XRCC1 genes and the effect of phenotype in patients with gastric cancer (2019)
- TBC1D8B Mutations Implicate RAB11-Dependent Vesicular Trafficking in the Pathogenesis of Nephrotic Syndrome (2019)
- Differential expression of inflammasome regulatory transcripts in periodontal disease (2019)
- Retrospective Investigation of Interleukin 1 and 6 Gene Polymorphism among Elderly Patients with Sarcopenia in the Turkish Population (2018)
- Genetic Analysis of Phenylketonuria Patients Treated with sapropterin. (2018)
- Fallot Tetralojili Olgularda Genetik Varyasyon Klinik Sonuçları Nasıl Etkiliyor? (2018)
- Fallot tetralojili hastalarda Genetik varyasyon klinik sonuçları nasıl etkiliyor? (2018)
- Türk Populasyonundaki Sarkopenik Yaşlılarda IL-1,IL-6 Gen Polimorfizminin Retrospektif Olarak İncelenmesi: (2018)
- HOW DOES GENETIC VARIATIONS AFFECT CLINICALOUTCOMES IN TETRALOGY OF FALLOT CASES? (2018)
- Retrospective Investigation of Interleukin 1 and 6 Gene Polymorphism among Elderly Patients with Sarcopenia in the Turkish Population (2018)
- The effects of mesenchymal stem cell on the macrophage phenotype (2018)
- Infant onset severe complement‐mediated hemolytic uremic syndrome complicated by secondary sclerosing cholangitis (2018)
- HEREDITARY HYPOMAGNESAEMIA WITH SECONDARY HYPOCALCEMIA: REPORT OF TWO SIBLINGS WITH LONG-TERM FOLLOW-UP (2018)
- Kronik Menenjit ile seyreden Kronik İnfantil Nörolojik Kutanöz ve Artiküler Sendrom Olgusu (2018)
- CAPS HASTALARDA KANAKİNUMAB KULLANIMI ve KLİNİK ETKİNLİĞİ (2018)
- Children with autosomal dominant polycystic kidney disease:Single center experience. (2018)
- GENETICALLY INTERESTING FAMILY WITH NEPHROTICSYNDROME IN THREE SIBLINGS (2018)
- Effects of colchicine on gingival inflammation, apoptosis, and alveolar bone loss in experimental periodontitis (2018)
- The Associations between Sleep Quality, Chronic Disorders andCognitive Functions in Male and Female Elder Population inTurkey (2018)
- Fever-induced Brugada syndrome in a 9-year-old boy presenting with acute chest pain (2018)
- NPHS2 GENE MUTATIONS IN AZERBAIJAN CHILDREN WITH STEROID-RESISTANT NEPHROTIC SYNDROME (2018)
- A novel mutation of interleukin-1 receptor antagonist (IL1RN) in a DIRA patient from Turkey: Diagnosis and treatment (2018)
- A Rare Case of Cholestasis: Arthrogryposis, Renal Tubular Disorder and Cholestasis Syndrome (2018)
- Canakinumab treatment in Turkish Colchicine resistant patients. (2017)
- PODOSİT HÜCRE MODELİNDE PROTEİNÜRİDE, SLİT DİYAFRAM PROTEİNLERİ GENLERİNİN EKSPRESYONU VE FARMAKOLOJİK MODÜLASYONU (2017)
- Targeted NGS study in 120 patients from Turkish population with autoinflammatory symptoms without MEFV gene mutations. (2017)
- CLINICAL SIGNIFICANCE OF GENETIC IN PATIENTS WITH C3 GLOMERULOPATHIES (2017)
- The Effect of Growth Hormone Therapy on Plasma Phenylalanine Level in Patient with Phenylketonuria: Case Report (2017)
- Büyüme Hormonu Tedavisinin Plazma Fenilalanini Üzerine Etkisi: Olgu Sunumu (2017)
- KOLŞİSİNE DİRENÇLİ AİLEVİ AKDENİZ ATEŞİ OLGULARININ KANAKİNUMAB İLE BAŞARILI YÖNETİMİ (2017)
- The Role of NEU1 Gene İn The Etiopathogenesis of Henoch Schönlein Vasculitis and İts Relationship with Renal Involvement (2017)
- IgM Yüksekliğinin Eşlik Ettiği Primer İmmün Yetmezlik Olgularımız: Tek Merkez Deneyimi (2017)
- Biochemical and Genetic Investigation of Phenylketonuria Patients Treated with Sapropterin (2017)
- Hemolytic uremic syndrome with multiple organ involvement secondary to complement factor H p.Arg1215X mutation (2017)
- Common SPINK-1 genetic mutations do not predispose to Crohn disease (2017)
- Advillin acts upstream of phospholipase C ϵ1 in steroid-resistant nephrotic syndrome (2017)
- Treatment of Familial Mediterranean Fever with Canakinumab in Patients Unresponsive to Colchicine (2017)
- ASSESSMENT OF SYSTEMIC VASCULAR INVOLVEMENT IN CHILDREN WITH UVEITIS (2017)
- Associatation of Thrombomodulin -1748 G/C Polymorphism and Plasma Thrombomodulin with Diabetic Microvascular Complications (2017)
- THE ROLE OF NEU1 GENE IN THE ETIOPATHOGENESIS OF HENOCH SCHONLEIN VASCULITIS AND ITS RELATIONSHIP WITH RENAL INVOLVEMENT (2017)
- DISTAL RENAL TUBULAR ACIDOSIS WITH TRANSIENT PROFOUND HYPERCALCEMIA IN TWO SIBLINGS (2017)
- NGS method in genetic autoinflammatory disease. (2017)
- CLINICAL SIGNIFICANCE OF GENETIC VARIANTS IN PATIENTS WITH C3 GLOMERULOPATHIES (2017)
- Sleep qualıty and related factors ın the elderly. (2017)
- Association of Thrombomodulin-1748 G/C polymorphism and plasma thrombomodulin with diabetic microvascular complications (2017)
- The relationship of Interleukin-6 -174 G > C gene polymorphism in type 2 diabetic patients with and without diabetic foot ulcers in Turkish population (2017)