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SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler
Examination of antinuclear antibody staining patterns and titers in patients with childhood-onset systemic lupus erythematosus
Current treatment in macrophage activation syndrome worldwide: a systematic literature review to inform the METAPHOR project
Interleukin (IL)-1/IL-6-Inhibitor-Associated Drug Reaction With Eosinophilia and Systemic Symptoms (DReSS) in Systemic Inflammatory Illnesses
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE
, cilt.12, sa.11, ss.2996-3020, 2024 (SCI-Expanded)
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Telemedicine in pediatric rheumatology: the video pediatric gait, arms, legs, and spine (v-pGALS) examination
FAMILIAL MEDITERRANEAN FEVER FROM CHILDHOOD TO ADULTHOOD
CLINICAL AND EXPERIMENTAL RHEUMATOLOGY
, sa.10, 2024 (SCI-Expanded)
Comparison of EULAR/PRINTO/PReS Ankara 2008 and 2022 ACR/EULAR classification criteria for granulomatosis with polyangiitis in children
The past 25 years in paediatric rheumatology: insights from monogenic diseases
The Potential Role of Cell-Death Mechanisms in the Pathogenesis of Familial Mediterranean Fever Attacks: Granzyme A and Beyond
Defining Criteria for Disease Activity States in Systemic Juvenile Idiopathic Arthritis Based on the Systemic Juvenile Arthritis Disease Activity Score
Impact of serological activity on flare following clinically inactive disease and remission in childhood-onset systemic lupus erythematosus
Identifying Specific Criteria for Juvenile Systemic Sclerosis: A Comparison of Adult and Pediatric Ratings
ARTHRITIS & RHEUMATOLOGY
, ss.4426-4429, 2024 (SCI-Expanded)
Diagnosis and Management of Pediatric Neuropsychiatric Systemic Lupus Erythematosus: An Update
A clinical overview of paediatric sarcoidosis: Multicentre experience from Turkey
Subclinical enthesitis in enthesitis-related arthritis and sacroiliitis associated with familial Mediterranean fever
A score for predicting colchicine resistance at the time of diagnosis in familial Mediterranean fever: data from the TURPAID registry
Rhupus syndrome in children: A multi-center retrospective cohort study and literature review
Acute kidney injury in children with moderate-severe COVID-19 and multisystem inflammatory syndrome in children: a referral center experience
Biologic drugs in the treatment of juvenile dermatomyositis: a literature review
Other Immunomodulatory Treatment for Cytokine Storm Syndromes
Evaluation of clinical outcomes in systemic juvenile idiopathic arthritis patients treated with biological agents in Turkey: The TURSIS study
Clinical and Experimental Rheumatology
, cilt.42, sa.1, ss.194-201, 2024 (SCI-Expanded)
Chronic non-bacterial osteomyelitis and immune checkpoint molecules
Is it possible to predict a disease course prone to macrophage activation syndrome at systemic juvenile idiopathic arthritis diagnosis?
Drug-induced lupus erythematosus in childhood: Case-based review
Possible Role of Dysbiosis of the Gut Microbiome in SLE
Feasibility of canakinumab withdrawal in colchicine-resistant familial Mediterranean fever
Treatment with Biologic Drugs in Pediatric Behçet’s Disease: A Comprehensive Analysis of the Published Data
Validation of the PEDiatric Behcet's Disease Classification Criteria (PEDBD): An International Consensus-based Approach
ARTHRITIS & RHEUMATOLOGY
, ss.2400-2402, 2023 (SCI-Expanded)
Thrombotic Manifestations in Pediatric Behcet Disease Patients: A Multicentre Comparative Study from EUROFEVER Registry
ARTHRITIS & RHEUMATOLOGY
, ss.2440-2441, 2023 (SCI-Expanded)
Feasibility of Conducting Comparative Effectiveness Research and Validation of a Clinical Disease Activity Score for Chronic Nonbacterial Osteomyelitis
Pediatric mixed connective tissue disease versus other overlap syndromes: a retrospective multicenter cohort study
Neuropsychiatric involvement in juvenile-onset systemic lupus erythematosus: A multicenter study
Rice bodies in children with rheumatic disorders: A case series and systematic literature review
Evaluation and Management of Deficiency of Adenosine Deaminase 2: An International Consensus Statement
Plasma Proteomic Analysis Reveals the Potential Role of Lectin and Alternative Complement Pathways in IgA Vasculitis Pathogenesis
The Characteristics of Patients With COVID-19–Associated Pediatric Vasculitis: An International, Multicenter Study
Evaluation of periodontal status and cytokine response in children with familial Mediterranean fever or systemic juvenile idiopathic arthritis
Report of 2 pediatric cases with atypical Cogan's syndrome and a systematic review
International Journal of Rheumatic Diseases
, cilt.26, sa.3, ss.544-550, 2023 (SCI-Expanded)
A new tool supporting the diagnosis of childhood-onset Behcet's disease: venous wall thickness
Claude Syndrome in Childhood Associated with Probable Neuro-Behcet Disease
Interstitial lung disease in autoinflammatory disease in childhood: A systematic review of the literature
A Child with Refractory and Relapsing Anti-3-Hydroxy-3-Methylglutaryl-Coenzyme A Reductase Myopathy: Case-Based Review
The pyrin inflammasome, a leading actor in pediatric autoinflammatory diseases
A novel variant in severe disease of DADA2: involving vasculitic and haematologic features
Risk factors for coronary arterial involvement in Turkish children with Kawasaki disease: a multicenter retrospective study
Neutrophil-to-Lymphocyte Ratio: An Easy Marker for the Diagnosis and Monitoring of Inflammatory Bowel Disease in Children
A patient-driven registry on Behçet’s disease: the AIDA for patients pilot project
Spontaneous hyphema in juvenile idiopathic arthritis uveitis
Galantamine attenuates autoinflammation in a mouse model of familial mediterranean fever
Treatment of childhood-onset Takayasu arteritis: switching between anti-TNF and anti-IL-6 agents
ACUTE KIDNEY INJURY ASSOCIATED WITH COVID-19 AND MULTISYSTEM INFLAMMATORY SYNDROME IN CHILDREN (MIS-C)
PEDIATRIC NEPHROLOGY
, cilt.37, sa.11, ss.2804, 2022 (SCI-Expanded)
The challenges in diagnosing pediatric primary antiphospholipid syndrome
Bradypnea in a child taking tumor necrosis factor-alpha inhibitors
Secukinumab in enthesitis-related arthritis and juvenile psoriatic arthritis: a randomised, double-blind, placebo-controlled, treatment withdrawal, phase 3 trial
ANNALS OF THE RHEUMATIC DISEASES
, cilt.82, sa.1, ss.154-160, 2022 (SCI-Expanded)
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Differences and similarities of proliferative and non-proliferative forms of biopsy-proven lupus nephritis: Single centre, cross-disciplinary experience
Probiotic use in the prophylaxis of periodic fever, aphthous stomatitis, pharyngitis, and adenitis (PFAPA) syndrome: a retrospective cohort study
The 2021 EULAR/American College of Rheumatology Points to Consider for Diagnosis, Management and Monitoring of the Interleukin-1 Mediated Autoinflammatory Diseases: Cryopyrin-Associated Periodic Syndromes, Tumour Necrosis Factor Receptor-Associated Periodic Syndrome, Mevalonate Kinase Deficiency, and Deficiency of the Interleukin-1 Receptor Antagonist
Assessment of systemic and ocular inflammation in juvenile idiopathic arthritis via choroidal vascularity index
Neurologic manifestations in children with COVID-19
IgG4-related disease in pediatric patients: a single-center experience.
Human OTULIN haploinsufficiency impairs cell-intrinsic immunity to staphylococcal alpha-toxin
Familial Mediterranean Fever: How to Interpret Genetic Results? How to Treat? A Quarter of a Century After the Association with the Mefv Gene
Long-term renal survival of paediatric patients with lupus nephritis
Nephrology Dialysis Transplantation
, cilt.37, sa.6, ss.1069-1077, 2022 (SCI-Expanded)
The performances of the ILAR, ASAS, and PRINTO classification criteria in ERA patients: a comparison study
New-Onset Ocular Myasthenia after Multisystem Inflammatory Syndrome in Children
The 2021 EULAR and ACR points to consider for diagnosis and management of autoinflammatory type I interferonopathies: CANDLE/PRAAS, SAVI and AGS
ANNALS OF THE RHEUMATIC DISEASES
, cilt.81, sa.5, ss.601-613, 2022 (SCI-Expanded)
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Macrophage activation syndrome in pediatric Sjogren's syndrome
Polyarteritis nodosa
Identification of a shared genetic risk locus for Kawasaki disease and immunoglobulin A vasculitis by a cross-phenotype meta-analysis
Spinal involvement in juvenile idiopathic arthritis: what do we miss without imaging?
The clinical course of SARS-CoV-2 infection among children with rheumatic disease under biologic therapy: a retrospective and multicenter study
Subcutaneous nodules as a clinical biomarker of Farber disease
Farber disease clinical impact: Patient reported outcomes as a measure of disease burden
International Consensus for the Dosing of Corticosteroids in Childhood-Onset Systemic Lupus Erythematosus With Proliferative Lupus Nephritis
Comparison of IVIG resistance predictive models in Kawasaki disease
Two siblings with Majeed syndrome and neutropenia
Glomerulonephritis with crescents in childhood; etiologies and significance of M2 macrophages
Real-world data on MTX tolerance with regimens used in children versus adults
Deubiquitination of proteasome subunits by OTULIN regulates type I IFN production
Juvenile idiopathic arthritis: lymphocyte activation gene-3 is a central immune receptor in children with oligoarticular subtypes
TAKAYASU ARTERITIS WITH RENAL ARTERY INVOLVEMENT IN CHILDREN: 12 YEARS EXPERIENCE OF A TERTIARY CENTER
PEDIATRIC NEPHROLOGY
, cilt.36, sa.10, ss.3441, 2021 (SCI-Expanded)
Hematopoietic Cell Transplantation Cures Adenosine Deaminase 2 Deficiency: Report on 30 Patients
JOURNAL OF CLINICAL IMMUNOLOGY
, cilt.41, sa.7, ss.1633-1647, 2021 (SCI-Expanded)
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Clinical spectrum of children with interstitial pneumonia with autoimmune features
Hematological involvement in pediatric systemic lupus erythematosus: A multi-center study
Mycophenolate Mofetil Versus Cyclophosphamide for Remission Induction in Childhood Polyarteritis Nodosa: An Open-Label, Randomized, Bayesian Noninferiority Trial
Update in familial Mediterranean fever
Defining colchicine resistance/intolerance in patients with familial Mediterranean fever: a modified-Delphi consensus approach.
The role of vascular inflammation markers in deficiency of adenosine deaminase 2
Wind of Change in the Treatment of Childhood-Onset Takayasu Arteritis: a Systematic Review
Penile involvement of immunoglobulin a vasculitis/Henoch-Schonlein purpura
Hemophagocytosis in bone marrow aspirates in multisystem inflammatory syndrome in children
The performances of the ACR 1997, SLICC 2012, and EULAR/ACR 2019 classification criteria in pediatric systemic lupus erythematosus.
Oral health status in children with familial Mediterranean fever
Esmeray P., İLERİ KEÇELİ T., UZAMIŞ TEKÇİÇEK M., BATU AKAL E. D., Arici Z. S., KONŞUK ÜNLÜ H., et al.
Biological classification of childhood arthritis: roadmap to a molecular nomenclature
Genetic disorders with symptoms mimicking rheumatologic diseases: A single-center retrospective study
Is Takayasu's arteritis more severe in children?
Whole exome sequencing in unclassified autoinflammatory diseases: more monogenic diseases in the pipeline?
Pulmonary Manifestations of Systemic Vasculitis in Children
Performances of the "MS-score" And "HScore" in the diagnosis of macrophage activation syndrome in systemic juvenile idiopathic arthritis patients
Clinical features, muscle biopsy scores, myositis specific antibody profiles and outcome in juvenile dermatomyositis.
Kawasaki-like disease in children with COVID-19.
Rheumatology international
, cilt.40, ss.2105-2115, 2020 (SCI-Expanded)
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- Citation Indexes: 69
- Patent Family Citations: 1
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Predictive biomarkers of IgA vasculitis with nephritis by metabolomic analysis
Seminars in Arthritis and Rheumatism
, cilt.50, sa.6, ss.1238-1244, 2020 (SCI-Expanded)
How the COVID-19 pandemic has influenced pediatric rheumatology practice: Results of a global, cross-sectional, online survey.
Seminars in arthritis and rheumatism
, cilt.50, ss.1262-1268, 2020 (SCI-Expanded)
PlumX Metrics
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- Policy Citations: 1
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Analysis of polymorphisms in the colchicine binding site of tubulin in colchicine-resistant familial Mediterranean fever patients.
Anti-IL1 treatment in colchicine-resistant paediatric FMF patients: real life data from the HELIOS registry.
Vasculitis as a Major Morbidity Factor in Patients With Partial RAG Deficiency
Long-term efficacy and safety of canakinumab in patients with colchicine-resistant familial Mediterranean fever: results from the randomised phase III CLUSTER trial
ASAH1pathogenic variants associated with acid ceramidase deficiency: Farber disease and spinal muscular atrophy with progressive myoclonic epilepsy
Takayasu arteritis presenting with spontaneous pneumothorax
Ancient familial Mediterranean fever mutations in human pyrin and resistance to Yersinia pestis.
Nature immunology
, cilt.21, sa.8, ss.857-867, 2020 (SCI-Expanded)
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- News Mentions: 17
Implications of COVID-19 in pediatric rheumatology
Epigenetics for Clinicians from the Perspective of Pediatric Rheumatic Diseases.
Comorbidities in familial Mediterranean fever: analysis of 2000 genetically confirmed patients.
Characteristics of pediatric Behcet's disease in Turkey and Israel: A cross-sectional cohort comparison
Common genetic susceptibility loci link PFAPA syndrome, Behcet's disease, and recurrent aphthous stomatitis
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
, cilt.117, sa.25, ss.14405-14411, 2020 (SCI-Expanded)
Childhood vasculitis
Autoinflammation in addition to combined immunodeficiency: SLC29A3 gene defect
The Initial Treatment of Systemic Juvenile Idiopathic Arthritis: An International Collaboration Among 10 Registries
ARTHRITIS & RHEUMATOLOGY
, cilt.72, ss.162-165, 2020 (SCI-Expanded)
Clusters in Pediatric Rheumatic Diseases
ISSAID/EMQN Best Practice Guidelines for the Genetic Diagnosis of Monogenic Autoinflammatory Diseases in the Next-Generation Sequencing Era
CLINICAL CHEMISTRY
, cilt.66, sa.4, ss.525-536, 2020 (SCI-Expanded)
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A rare cause of steroid-resistant nephrotic syndrome in a child: Answers
Distinct interferon signatures and cytokine patterns define additional systemic autoinflammatory diseases
A rare cause of steroid resistant nephrotic syndrome in a child: Questions
A clinical score to guide in decision making for monogenic type I IFNopathies.
Performance of the new 'Eurofever/PRINTO classification criteria' in FMF patients.
Rheumatological manifestations in inborn errors of immunity
A Monogenic Disease with a Variety of Phenotypes: Deficiency of Adenosine Deaminase 2
What's new in autoinflammation?
Toward the elimination of bias in Pediatric Research
Emergent high fatality lung disease in systemic juvenile arthritis
Systemic onset juvenile idiopathic arthritis: a single center experience
Testing the Model for Predicting Effectiveness of Anakinra in Systemic Juvenile Idiopathic Arthritis
Target Organ Associations in Polyarteritis Nodosa (PAN): Results of a Worldwide Collaboration Study
ARTHRITIS & RHEUMATOLOGY
, cilt.71, 2019 (SCI-Expanded)
European consensus-based recommendations for diagnosis and treatment of immunoglobulin A vasculitis-the SHARE initiative
RHEUMATOLOGY
, cilt.58, sa.9, ss.1607-1616, 2019 (SCI-Expanded)
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Classification criteria for autoinflammatory recurrent fevers
ANNALS OF THE RHEUMATIC DISEASES
, cilt.78, sa.8, ss.1025-1032, 2019 (SCI-Expanded)
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- Citation Indexes: 354
- Policy Citations: 1
- Clinical Citations: 1
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The European network for care of children with paediatric rheumatic diseases: care across borders
Cancer incidence in familial Mediterranean fever patients: a retrospective analysis from central Anatolia
Clinical and histopathological prognostic factors affecting the renal outcomes in childhood ANCA-associated vasculitis
Deficiency of adenosine deaminase 2; special focus on central nervous system imaging
European consensus-based recommendations for the diagnosis and treatment of rare paediatric vasculitides - the SHARE initiative
An International Delphi Survey for the Definition of New Classification Criteria for Familial Mediterranean Fever, Mevalonate Kinase Deficiency, TNF Receptor-associated Periodic Fever Syndromes, and Cryopyrin-associated Periodic Syndrome
European consensus-based recommendations for the diagnosis and treatment of Kawasaki disease - the SHARE initiative
RHEUMATOLOGY
, cilt.58, sa.4, ss.672-682, 2019 (SCI-Expanded)
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Tocilizumab treatment in juvenile idiopathic arthritis patients: A single center experience
Alternative Therapies for Cytokine Storm Syndromes
Is age associated with disease severity and compliance to treatment in children with familial Mediterranean fever?
Chronic recurrent multifocal osteomyelitis in children: a single center experience over five years.
Concurrence of juvenile idiopathic arthritis and primary demyelinating disease in a young child
Vasculitis in Systemic Autoinflammatory Diseases
Anakinra treatment in macrophage activation syndrome: a single center experience and systemic review of literature
Genetic testing for DADA2: How can we avoid missing patients?
EUROPEAN JOURNAL OF HUMAN GENETICS
, cilt.26, sa.11, ss.1563-1564, 2018 (SCI-Expanded)
A patient heterozygous for R92Q mutation with periodic fever and aphthous stomatitis, pharyngitis, and adenitis (PFAPA) syndrome-like phenotype
In silico validation of the Autoinflammatory Disease Damage Index
ANNALS OF THE RHEUMATIC DISEASES
, cilt.77, sa.11, ss.1599-1605, 2018 (SCI-Expanded)
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Familial Mediterranean fever patients homozygous for E148Q variant may have milder disease
INTERNATIONAL JOURNAL OF RHEUMATIC DISEASES
, cilt.21, sa.10, ss.1857-1862, 2018 (SCI-Expanded)
Towards a new set of classification criteria for PFAPA syndrome
Clinical Features and Outcome of Patients with Polyarteritis Nodosa - a Global Collaborative Study
ARTHRITIS & RHEUMATOLOGY
, cilt.70, 2018 (SCI-Expanded)
Vasculitis Pathogenesis: Can We Talk About Precision Medicine?
IL1RN Variation Influences Both Disease Susceptibility and Response to Recombinant Human Interleukin-1 Receptor Antagonist Therapy in Systemic Juvenile Idiopathic Arthritis
Consensus Treatment Plans for Chronic Nonbacterial Osteomyelitis Refractory to Nonsteroidal Antiinflammatory Drugs and/or With Active Spinal Lesions
JAK1/2 inhibition with baricitinib in the treatment of autoinflammatory interferonopathies
JOURNAL OF CLINICAL INVESTIGATION
, cilt.128, sa.7, ss.3041-3052, 2018 (SCI-Expanded)
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A20 haploinsufficiency (HA20): clinical phenotypes and disease course of patients with a newly recognised NF-kB-mediated autoinflammatory disease
Update on the epidemiology and disease outcome of Familial Mediterranean fever
BEST PRACTICE & RESEARCH IN CLINICAL RHEUMATOLOGY
, cilt.32, sa.2, ss.254-260, 2018 (SCI-Expanded)
The Turkish version of the Juvenile Arthritis Multidimensional Assessment Report (JAMAR)
Blau Syndrome-Associated Uveitis: Preliminary Results From an International Prospective Interventional Case Series
Pediatric forms of vasculitis
BEST PRACTICE & RESEARCH IN CLINICAL RHEUMATOLOGY
, cilt.32, sa.1, ss.137-147, 2018 (SCI-Expanded)
Acceptability and Practicality of the Turkish Translation of Pediatric Gait Arm Legs and Spine in Turkish Children
European evidence-based recommendations for the diagnosis and treatment of childhood-onset lupus nephritis: the SHARE initiative
ANNALS OF THE RHEUMATIC DISEASES
, cilt.76, sa.12, ss.1965-1973, 2017 (SCI-Expanded)
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Assessment of autonomic functions in children with familial Mediterranean fever by using heart rate variability measurements
INTERNATIONAL JOURNAL OF RHEUMATIC DISEASES
, cilt.20, sa.12, ss.2086-2092, 2017 (SCI-Expanded)
A clinical update on inflammasomopathies.
European evidence-based recommendations for diagnosis and treatment of childhood-onset systemic lupus erythematosus: the SHARE initiative.
Annals of the rheumatic diseases
, cilt.76, ss.1788-1796, 2017 (SCI-Expanded)
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- Citation Indexes: 155
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Multi-National Observational Patient Diary Study to Assess Disease Burden of Periodic Fever Syndromes (PFS), Including Colchicine-Resistant Familial Mediterranean Fever (crFMF), TNF-Receptor Associated Periodic Syndrome (TRAPS) and Mevalonate Kinase Deficiency (MKD)
ARTHRITIS & RHEUMATOLOGY
, cilt.69, 2017 (SCI-Expanded)
European evidence-based recommendations for diagnosis and treatment of paediatric antiphospholipid syndrome: the SHARE initiative
Interferon Signature in Childhood Rheumatic Diseases
ARTHRITIS & RHEUMATOLOGY
, cilt.69, 2017 (SCI-Expanded)
Unusual Presentations of Childhood Systemic Lupus Erythematosus to the Emergency Department.
Recent advances in childhood vasculitis.
Colchicine resistance and intolerance in familial mediterranean fever: Definition, causes, and alternative treatments
Comparing polyarteritis nodosa in children and adults: a single center study
INTERNATIONAL JOURNAL OF RHEUMATIC DISEASES
, cilt.20, sa.8, ss.1016-1022, 2017 (SCI-Expanded)
Monogenic Periodic Fever Syndromes: Treatment Options for the Pediatric Patient.
Childhood systemic vasculitis
BEST PRACTICE & RESEARCH IN CLINICAL RHEUMATOLOGY
, cilt.31, sa.4, ss.558-575, 2017 (SCI-Expanded)
Gastrointestinal system manifestations in juvenile systemic lupus erythematosus
Autoinflammatory Diseases with Periodic Fevers.
Diagnostic criteria for cryopyrin-associated periodic syndrome (CAPS)
Kuemmerle-Deschner J. B., ÖZEN S., Tyrrell P. N., Kone-Paut I., Goldbach-Mansky R., Lachmann H., et al.
ANNALS OF THE RHEUMATIC DISEASES
, cilt.76, sa.6, ss.942-947, 2017 (SCI-Expanded)
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- Clinical Citations: 3
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The changing face of polyarteritis nodosa and necrotizing vasculitis.
Development of the autoinflammatory disease damage index (ADDI)
ANNALS OF THE RHEUMATIC DISEASES
, cilt.76, sa.5, 2017 (SCI-Expanded)
PlumX Metrics
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- Citation Indexes: 68
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Genetic architecture distinguishes systemic juvenile idiopathic arthritis from other forms of juvenile idiopathic arthritis: clinical and therapeutic implications
ANNALS OF THE RHEUMATIC DISEASES
, cilt.76, sa.5, 2017 (SCI-Expanded)
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Correlation and Responsiveness of Cutaneous Lupus Disease Area and Severity Index and Skindex-29 with Cutaneous Childhood Lupus Erythematous
ARTHRITIS & RHEUMATOLOGY
, cilt.69, ss.144-145, 2017 (SCI-Expanded)
EULAR/PReS standards and recommendations for the transitional care of young people with juvenile-onset rheumatic diseases
ANNALS OF THE RHEUMATIC DISEASES
, cilt.76, sa.4, 2017 (SCI-Expanded)
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International Retrospective Chart Review of Treatment Patterns in Severe Familial Mediterranean Fever, Tumor Necrosis Factor Receptor-Associated Periodic Syndrome, and Mevalonate Kinase Deficiency/Hyperimmunoglobulinemia D Syndrome
Familial Mediterranean Fever: Recent Developments in Pathogenesis and New Recommendations for Management.
IgA vasculitis (Henoch-Schonlein): Case definition andguidelines for data collection, analysis, and presentation of immunisation safety data
Final diagnosis of children and adolescents with musculoskeletal complaints
Consensus-based recommendations for the management of juvenile dermatomyositis
ANNALS OF THE RHEUMATIC DISEASES
, cilt.76, sa.2, ss.329-340, 2017 (SCI-Expanded)
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Discontinuing colchicine in symptomatic carriers for MEFV (Mediterranean FeVer) variants
Tocilizumab treatment in childhood Takayasu arteritis: Case series of four patients and systematic review of the literature
IgA vasculitis (Henoch-Schonlein purpura) in children
Assessment of the HScore for reactive haemophagocytic syndrome in patients with rheumatic diseases
Periodic Fever, Aphthosis, Pharyngitis, and Adenitis Syndrome: Analysis of Patients From Two Geographic Areas.
Spontaneous reports of vasculitis as an adverse event following immunization: A descriptive analysis across three international databases
Vasculitis as an adverse event following immunization - Systematic literature review
VACCINE
, cilt.34, sa.51, ss.6641-6651, 2016 (SCI-Expanded)
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BehcEt's Disease in Children: Eastern Mediterranean Experience
ARTHRITIS & RHEUMATOLOGY
, cilt.68, 2016 (SCI-Expanded)
The Characteristic Features of the Patients with Deficiency of Adenosine Deaminase 2 (DADA2)
ARTHRITIS & RHEUMATOLOGY
, cilt.68, 2016 (SCI-Expanded)
Macrophage activation syndrome in children with systemic juvenile idiopathic arthritis and systemic lupus erythematosus
Whole Exome Sequencing in Early Onset Systemic Lupus Erythematosus
ARTHRITIS & RHEUMATOLOGY
, cilt.68, 2016 (SCI-Expanded)
Efficacy and Safety of Canakinumab in Patients with Colchicine-Resistant Familial Mediterranean Fever, Hyper-Immunoglobulin D Syndrome/Mevalonate Kinase Deficiency and TNF Receptor-Associated Periodic Syndrome: 40 Week Results from the Pivotal Phase 3 Umbrella Cluster Trial
ARTHRITIS & RHEUMATOLOGY
, cilt.68, 2016 (SCI-Expanded)
Biallelic hypomorphic mutations in a linear deubiquitinase define otulipenia, an early-onset autoinflammatory disease
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
, cilt.113, sa.36, ss.10127-10132, 2016 (SCI-Expanded)
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Consensus classification criteria for paediatric Behcet's disease from a prospective observational cohort: PEDBD
Development and initial validation of international severity scoring system for familial Mediterranean fever (ISSF)
What is the best acute phase reactant for familial Mediterranean fever follow-up and its role in the prediction of complications? A systematic review
EULAR recommendations for the management of familial Mediterranean fever
ANNALS OF THE RHEUMATIC DISEASES
, cilt.75, sa.4, ss.644-651, 2016 (SCI-Expanded)
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2016 Classification Criteria for Macrophage Activation Syndrome Complicating Systemic Juvenile Idiopathic Arthritis A European League Against Rheumatism/American College of Rheumatology/Paediatric Rheumatology International Trials Organisation Collaborative Initiative
ANNALS OF THE RHEUMATIC DISEASES
, cilt.75, sa.3, ss.481-489, 2016 (SCI-Expanded)
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Efficacy and safety of treatments in Familial Mediterranean fever: a systematic review
A comprehensive evaluation of sedimentary zeolites from Turkey as pozzolanic addition of cement- and lime-based binders
Failure to thrive, interstitial lung disease, and progressive digital necrosis with onset in infancy
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY
, cilt.74, sa.1, ss.186-189, 2016 (SCI-Expanded)
Performance of Different Diagnostic Criteria for Familial Mediterranean Fever in Children with Periodic Fevers: Results from a Multicenter International Registry
Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory disease
NATURE GENETICS
, cilt.48, sa.1, ss.67-75, 2016 (SCI-Expanded)
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Rate and Clinical Presentation of Macrophage Activation Syndrome in Patients With Systemic Juvenile Idiopathic Arthritis Treated With Canakinumab
HLA-DRB1*11 and variants of the MHC class II locus are strong risk factors for systemic juvenile idiopathic arthritis
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
, cilt.112, sa.52, ss.15970-15975, 2015 (SCI-Expanded)
Etanercept treatment in five cases of refractory chronic recurrent multifocal osteomyelitis (CRMO)
DECADE IN REVIEW- PAEDIATRIC RHEUMATOLOGY A field on the move
Phenotypic and genotypic characteristics of cryopyrin-associated periodic syndrome: a series of 136 patients from the Eurofever Registry
ANNALS OF THE RHEUMATIC DISEASES
, cilt.74, sa.11, ss.2043-2049, 2015 (SCI-Expanded)
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Lupus in a patient with cystinosis: is it drug induced?
Treatment of colchicine-resistant Familial Mediterranean fever in children and adolescents
Development and Validation of Diagnostic Criteria for Cryopyrin Associated Periodic Syndromes
KUEMMERLE-DESCHNER J. B., ÖZEN S., Tyrrell P. N., KONE-PAUT I., GOLDBACH-MANSKY R., Lachmann H., et al.
ARTHRITIS & RHEUMATOLOGY
, cilt.67, 2015 (SCI-Expanded)
HA20: A Novel Autoinflammatory Disease Caused By Haploinsufficiency of A20, Encoded By TNFAIP3
ARTHRITIS & RHEUMATOLOGY
, cilt.67, 2015 (SCI-Expanded)
Investigation of the inflammatory cell migration process in familial Mediterranean fever
Recommendations for the management of autoinflammatory diseases
ANNALS OF THE RHEUMATIC DISEASES
, cilt.74, sa.9, ss.1636-1644, 2015 (SCI-Expanded)
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CHARACTERISTICS OF RENAL TRANSPLANT CHILDREN WITH CHRONIC ALLOGRAFT NEPHROPATHY: EXPERIENCE OF A TERTIARY REFERRAL CENTER
PEDIATRIC NEPHROLOGY
, cilt.30, sa.9, ss.1721, 2015 (SCI-Expanded)
ANTI- INTERLEUKIN 1 TREATMENT IN SECONDARY RENAL AMYLOIDOSIS ASSOCIATED WITH AUTOINFLAMMATORY DISEASES
RITUXIMAB EXPERIENCE OF A TERTIARY REFERRAL CENTER FOR DIFFICULT-TO-TREAT NEPHROTIC SYNDROME
PEDIATRIC NEPHROLOGY
, cilt.30, sa.9, ss.1692, 2015 (SCI-Expanded)
Cochlear functions in children with familial Mediterranean fever: Any role of the severity of the disease?
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY
, cilt.79, sa.9, ss.1566-1570, 2015 (SCI-Expanded)
Vasculitis: do we know more to classify better?
Studying cytokines of T helper cells in the kidney disease of IgA vasculitis (Henoch-Schonlein purpura)
A Case Series of Adenosine Deaminase 2-deficient Patients Emphasizing Treatment and Genotype-phenotype Correlations
The myths we believed in familial Mediterranean fever: what have we learned in the past years?
Evidence-based provisional clinical classification criteria for autoinflammatory periodic fevers
ANNALS OF THE RHEUMATIC DISEASES
, cilt.74, sa.5, ss.799-805, 2015 (SCI-Expanded)
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Vasculitis in children
Evidence-based recommendations for genetic diagnosis of familial Mediterranean fever
ANNALS OF THE RHEUMATIC DISEASES
, cilt.74, sa.4, ss.635-641, 2015 (SCI-Expanded)
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Reviewing the Recommendations for Lupus in Children
Current therapeutic options for managing familial Mediterranean fever
Special Aspects of Familial Mediterranean Fever in Childhood
Validation of the Auto-Inflammatory Diseases Activity Index (AIDAI) for hereditary recurrent fever syndromes
ANNALS OF THE RHEUMATIC DISEASES
, cilt.73, sa.12, ss.2168-2173, 2014 (SCI-Expanded)
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Endothelial function in patients with familial Mediterranean fever-related amyloidosis and association with cardiovascular events
Clinical Features, Treatment, and Outcome of Macrophage Activation Syndrome Complicating Systemic Juvenile Idiopathic Arthritis A Multinational, Multicenter Study of 362 Patients
ARTHRITIS & RHEUMATOLOGY
, cilt.66, sa.11, ss.3160-3169, 2014 (SCI-Expanded)
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Evidence Based Recommendations for Genetic Diagnosis of Familial Mediterranean Fever.
ARTHRITIS & RHEUMATOLOGY
, cilt.66, 2014 (SCI-Expanded)
In vitro evaluation of effects of sustained anti-TNF release from MPEG-PCL-MPEG and PCL microspheres on human rheumatoid arthritis synoviocytes
Evidence Based Recommendations for the Management of Cryopyrin Associated Periodic Syndromes (CAPS)
ARTHRITIS & RHEUMATOLOGY
, cilt.66, 2014 (SCI-Expanded)
Evidence Based Recommendatinos for Diagnosis and Management of Mevalonate Kinase Deficiency (MKD)
ARTHRITIS & RHEUMATOLOGY
, cilt.66, 2014 (SCI-Expanded)
Thrombophilic Risk Factors And The Efficiency Of Prophylactic Anticoagulation Therapy In Children Who Underwent Renal Transplantation
PEDIATRIC NEPHROLOGY
, cilt.29, sa.9, ss.1694, 2014 (SCI-Expanded)
Studying Cytokines Of T Helper Cells In The Kidney Disease Of Iga Vasculitis (henoch-schonlein Purpura)
PEDIATRIC NEPHROLOGY
, cilt.29, sa.9, ss.1689, 2014 (SCI-Expanded)
Effects Of Eculizumab On Long-term Clinical Outcome Of Ahus Patients
PEDIATRIC NEPHROLOGY
, cilt.29, sa.9, ss.1818-1819, 2014 (SCI-Expanded)
Characterization and Evaluation of Triamcinolone, Raloxifene, and Their Dual-Loaded Microspheres as Prospective Local Treatment System in Rheumatic Rat Joints
JOURNAL OF PHARMACEUTICAL SCIENCES
, cilt.103, sa.8, ss.2396-2405, 2014 (SCI-Expanded)
Diagnostic validity of colchicine in patients with Familial Mediterranean fever
Human Procaspase-1 Variants with Decreased Enzymatic Activity Are Associated with Febrile Episodes and May Contribute to Inflammation via RIP2 and NF-kB Signaling
Studying IFN-gamma, IL-17 and FOXP3 in pediatric lupus nephritis
FMF50: a score for assessing outcome in familial Mediterranean fever
Clinical features of childhood granulomatosis with polyangiitis (wegener's granulomatosis)
Results from a multicentre international registry of familial Mediterranean fever: impact of environment on the expression of a monogenic disease in children
Early- Onset Stroke and Vasculopathy Associated with Mutations in ADA2
NEW ENGLAND JOURNAL OF MEDICINE
, cilt.370, sa.10, ss.911-920, 2014 (SCI-Expanded)
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A clinical guide to autoinflammatory diseases: familial Mediterranean fever and next-of-kin
Pediatric Onset of Behcet Syndrome
BEHCET'S SYNDROME: FROM PATHOGENESIS TO TREATMENT
, ss.165-176, 2014 (SCI-Expanded)
Rheumatic Inflammatory Eye Diseases of Childhood
RHEUMATIC DISEASE CLINICS OF NORTH AMERICA
, cilt.39, sa.4, ss.801-833, 2013 (SCI-Expanded)
Disease activity assessment in childhood vasculitis: development and preliminary validation of the Paediatric Vasculitis Activity Score (PVAS)
Therapeutic approaches for the treatment of renal disease in juvenile systemic lupus erythematosus: an international multicentre PRINTO study
Pediatric-onset Behçet disease.
The performance of the new SLICC criteria for the classification of SLE in children
PEDIATRIC NEPHROLOGY
, cilt.28, sa.8, ss.1548, 2013 (SCI-Expanded)
The Effect Of Fibroblast Growth Factor 23 On Left Ventricular Function In Peritoneal Dialysis Children
PEDIATRIC NEPHROLOGY
, cilt.28, sa.8, ss.1643, 2013 (SCI-Expanded)
CONTRIBUTORY RISK FACTORS FOR DEVELOPMENT OF THROMBOSIS IN CHILDRENWITH NEPHROTIC SYNDROME
PEDIATRIC NEPHROLOGY
, cilt.28, sa.8, ss.1584, 2013 (SCI-Expanded)
Treatment of autoinflammatory diseases: results from the Eurofever Registry and a literature review
ANNALS OF THE RHEUMATIC DISEASES
, cilt.72, sa.5, ss.678-685, 2013 (SCI-Expanded)
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The specificities of pediatric vasculitis classification
2012 Revised International Chapel Hill Consensus Conference Nomenclature of Vasculitides
ARTHRITIS AND RHEUMATISM
, cilt.65, sa.1, ss.1-11, 2013 (SCI-Expanded)
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Two Randomized Trials of Canakinumab in Systemic Juvenile Idiopathic Arthritis
NEW ENGLAND JOURNAL OF MEDICINE
, cilt.367, sa.25, ss.2396-2406, 2012 (SCI-Expanded)
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Severity scoring system for paediatric FMF
PERITONEAL DIALYSIS IN CHILDREN UNDER TWO YEARS OF AGE
PEDIATRIC NEPHROLOGY
, cilt.27, sa.9, ss.1799-1800, 2012 (SCI-Expanded)
ATYPICAL HUS AND ECULIZUMAB TREATMENT: EXPERIENCE OF A TERTIARY CENTER
PEDIATRIC NEPHROLOGY
, cilt.27, sa.9, ss.1630, 2012 (SCI-Expanded)
An International registry on Autoinflammatory diseases: the Eurofever experience
ANNALS OF THE RHEUMATIC DISEASES
, cilt.71, sa.7, ss.1177-1182, 2012 (SCI-Expanded)
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Canakinumab induces remission in a patient with resistant familial Mediterranean fever
Pediatric vasculitis.
Evaluation of the current disease severity scores in paediatric FMF: is it necessary to develop a new one?
Homozygous M694V as a risk factor for amyloidosis in Turkish FMF patients
Time to focus on outcome assessment tools for childhood vasculitis
OUTCOME OF NEPHROPATHIC CYSTINOSIS IN PEDIATRIC RENAL TRANSPLANTATION: A SINGLE CENTRE EXPERIENCE
PEDIATRIC TRANSPLANTATION
, cilt.15, ss.82, 2011 (SCI-Expanded)
Renal amyloidosis in children
COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness
JOURNAL OF CLINICAL INVESTIGATION
, cilt.121, sa.5, ss.2013-2024, 2011 (SCI-Expanded)
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Follow-Up of Patients With Juvenile Nephronophthisis After Renal Transplantation: A Single Center Experience
The Eurofever Project: towards better care for autoinflammatory diseases
Anti IL1 treatment for FMF patients resistant to colchicine: reasoning treatment from laboratory experience
CLINICAL AND EXPERIMENTAL RHEUMATOLOGY
, cilt.29, sa.2, ss.435, 2011 (SCI-Expanded)
Familial Mediterranean fever cases accompanied with central nervous system diseases
CLINICAL AND EXPERIMENTAL RHEUMATOLOGY
, cilt.29, sa.2, ss.405, 2011 (SCI-Expanded)
Macrophage Activating Syndrome complicating Wegener Granulomatosis: treatment with plasma exchange
CLINICAL AND EXPERIMENTAL RHEUMATOLOGY
, cilt.29, sa.2, ss.463, 2011 (SCI-Expanded)
Spondyloenchondrodysplasia with Systemic Lupus Erythematosus: a report of three cases
CLINICAL AND EXPERIMENTAL RHEUMATOLOGY
, cilt.29, sa.2, ss.430, 2011 (SCI-Expanded)
Anti-interleukin 1 treatment for patients with familial Mediterranean fever resistant to colchicine.
A preliminary score for the assessment of disease activity in hereditary recurrent fevers: results from the AIDAI (Auto-Inflammatory Diseases Activity Index) Consensus Conference
ANNALS OF THE RHEUMATIC DISEASES
, cilt.70, sa.2, ss.309-314, 2011 (SCI-Expanded)
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Pediatric Behcet's Disease and Thromboses
Registries in rheumatological and musculoskeletal conditions. Paediatric Behcet's disease: an international cohort study of 110 patients. One-year follow-up data
The Association of Inflammatory Bowel Disease and Mediterranean Fever Gene (MEFV) Mutations in Turkish Children
EULAR points to consider in the development of classification and diagnostic criteria in systemic vasculitis
The "other" vasculitis syndromes and kidney involvement
Pediatric onset Behcet disease
Decrease in the rate of secondary amyloidosis in Turkish children with FMF: are we doing better?
Predictors of poor response to methotrexate in polyarticular-course juvenile idiopathic arthritis: analysis of the PRINTO methotrexate trial
Stanozolol treatment for successful prevention of attacks of severe primary cryofibrinogenemia.
EULAR/PRINTO/PRES criteria for Henoch-Schonlein purpura, childhood polyarteritis nodosa, childhood Wegener granulomatosis and childhood Takayasu arteritis: Ankara 2008. Part II: Final classification criteria
ANNALS OF THE RHEUMATIC DISEASES
, cilt.69, sa.5, ss.798-806, 2010 (SCI-Expanded)
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Risk factors in community-acquired urinary tract infections caused by ESBL-producing bacteria in children
EULAR/PRINTO/PRES criteria for Henoch-Schonlein purpura, childhood polyarteritis nodosa, childhood Wegener granulomatosis and childhood Takayasu arteritis: Ankara 2008. Part I: Overall methodology and clinical characterisation
ANNALS OF THE RHEUMATIC DISEASES
, cilt.69, sa.5, ss.790-797, 2010 (SCI-Expanded)
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Preventing tuberculosis in children receiving anti-tnf treatment
Behçet disease: treatment of vascular involvement in children.
Low cortisol levels in active juvenile idiopathic arthritis.
Clinical and radiographic findings in two brothers affected with a novel mutation in matrix metalloproteinase 2 gene
Anti-IL-1 treatment for secondary amyloidosis in an adolescent with FMF and Behcet's disease
The use of low-dose cyclophosphamide followed by AZA/MMF treatment in childhood lupus nephritis.
Childhood vasculitis: new insights into classification and therapy
SCANDINAVIAN JOURNAL OF RHEUMATOLOGY
, cilt.39, ss.14, 2010 (SCI-Expanded)
Genotoxicity of Anti-Tumor Necrosis Factor Therapy in Patients With Juvenile Idiopathic Arthritis
Macrophage Activation Syndrome in Juvenile Systemic Lupus Erythematosus A Multinational Multicenter Study of Thirty-Eight Patients
Genetic diagnosis by whole exome capture and massively parallel DNA sequencing
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
, cilt.106, sa.45, ss.19096-19101, 2009 (SCI-Expanded)
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Increased Frequency of Extremely Skewed X Chromosome Inactivation in Juvenile Idiopathic Arthritis
Update in paediatric vasculitis.
Best practice & research. Clinical rheumatology
, cilt.23, ss.679-88, 2009 (SCI-Expanded)
Ulcerative colitis associated with Takayasu's arteritis in a child
Biologic therapy in primary systemic vasculitis of the young
Changing Concepts in Familial Mediterranean Fever: Is It Possible to Have an Autosomal-Recessive Disease With Only One Mutation?
A new set of criteria for the diagnosis of familial Mediterranean fever in childhood
RHEUMATOLOGY
, cilt.48, sa.4, ss.395-398, 2009 (SCI-Expanded)
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Disease severity in children and adolescents with familial Mediterranean fever: a comparative study to explore environmental effects on a monogenic disease
Musculoskeletal sonography in juvenile systemic lupus erythematosus.
MEFV mutations in systemic onset juvenile idiopathic arthritis
Characterization of large rearrangements in autosomal dominant polycystic kidney disease and the PKD1/TSC2 contiguous gene syndrome
KIDNEY INTERNATIONAL
, cilt.74, sa.11, ss.1468-1479, 2008 (SCI-Expanded)
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A very frequent mutation and remarkable association of R761H with M694V mutations in Turkish familial Mediterranean fever patients
Eye involvement in children with primary focal segmental glomerulosclerosis
Pathogenesis-related adhesion molecules in Henoch-Schonlein vasculitis
Triple immunosuppression with tacrolimus in pediatric renal transplantation: Single-center experience
Renal transplantation in children with lower urinary tract dysfunction of different origin: A single-center experience
Henoch-Schonlein Purpura, Polyarteritis Nodosa, Wegener's Granulomatosis, and Other Vasculitides
Prevalence of the MEFV gene mutations in childhood polyarteritis nodosa
A patient with hyper-IgD syndrome responding to anti-TNF treatment
Is the CD14 C159T polymorphism effective in the development of secondary amyloidosis in Familial Mediterranean fever?
The association of inflammatory bowel disease and familial Mediterranean fever in Turkish children
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION
, cilt.44, ss.106, 2007 (SCI-Expanded)
An overlap syndrome involving autoimmune hepatitis and systemic lupus erythematosus in childhood
Colchicine use in children and adolescents with familial Mediterranean fever: Literature review and consensus statement
Childhood vasculitides in Turkey: a nationwide survey
Extranodal type T/NK-cell lymphoma with an atypical clinical presentation
A new international classification of childhood vasculitis
A multicenter study of patients with adult-onset Still's disease compared with systemic juvenile idiopathic arthritis
CLINICAL RHEUMATOLOGY
, cilt.25, sa.5, ss.639-644, 2006 (SCI-Expanded)
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Reversible posterior leukoencephalopathy syndrome: report of three cases.
Problems in classifying vasculitis in children
Women in Academic Rheumatology
Four-month-old infant with focal segmental glomerulosclerosis and mitochondrial DNA deletion
Beneficial role of intravenous calcitriol on bone mineral density in children with severe secondary hyperparathyroidism
Pyrin Q148 mutation and familial Mediterranean fever
QJM-AN INTERNATIONAL JOURNAL OF MEDICINE
, cilt.95, sa.5, ss.332-333, 2002 (SCI-Expanded)
Diğer Dergilerde Yayınlanan Makaleler
Differentiating Multisystem Inflammatory Syndrome in Children from Kawasaki Disease During the Pandemic
The Comparison of Pediatric Patients with Familial Mediterranean Fever Originated from Turkey and Crimea
Rare Autoinflammatory Diseases
Measuring Vasculitis with Numbers: Outcome Scores
Behcet's disease in children: single-center experience
TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS
, cilt.54, sa.3, ss.179-184, 2019 (ESCI)
Vasculitis: Decade in Review
Traitement par étanercept de cinq cas d'ostéomyélite multifocale chronique récurrente (OMCR) réfractaires
Familial Mediterranean fever: current perspectives
Familial Mediterranean Fever, Polyarteritis Nodosa and Mefv Mutations
TURKISH NEPHROLOGY DIALYSIS AND TRANSPLANTATION JOURNAL
, cilt.22, sa.1, ss.68-71, 2013 (ESCI)
Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar
The role of DNA methylation for disease severity in patients with heterozygous mutations in the Mediterranean Fever Gene MEFV
56th Annual Conference of the European-Society-of-Human-Genetics (ESHG), Glasgow, İngiltere, 10 - 13 Haziran 2023, ss.613-614
INVESTIGATION OF THE EFFECTS OF HEALTH LITERACY LEVELS OF PATIENTS WITH JUVENILE IDIOPATHIC ARTHRITIS AND THEIR FAMILIES ON THE GENERAL HEALTH STATUS, QUALITY OF LIFE AND PHYSICAL FUNCTION CAPACITY OF THE PATIENTS
EULAR 2023, Milan, İtalya, 31 Mayıs 2023, cilt.82, ss.1936
THE NAILFOLD VIDEOCAPILLAROSCOPY IN PEDIATRIC BEHCET'S DISEASE: A MULTI-CENTER STUDY
2nd PAFLAR Congress on Paediatric Rheumatology in Africa - Challenge, Innovate and Grow, ELECTR NETWORK, 29 Haziran - 01 Temmuz 2022, cilt.61
Validation of the Eular/ACR 2017 idiopathic inflammatory myopathy classification criteria in JDM patients
Pediatric Rheumatology European Society (PReS) e-Congress-2020, BİLİNMEYEN ÜLKELER (DİĞER), 23 - 26 Eylül 2020, cilt.18, ss.54
A PILOT PROTEOMIC ANALYSIS OF PLASMA BIOMARKERS IN IGA VASCULITIS
Annual European Congress of Rheumatology (EULAR), ELECTR NETWORK, 03 Haziran 2020, cilt.79, ss.1200-1201
Farber disease (acid ceramidase deficiency) natural history study: Prospective and retrospective clinical data
16th Annual Research Meeting of the WORLDSymposium(TM), Florida, Amerika Birleşik Devletleri, 10 - 14 Şubat 2020, cilt.129
AB0574 A MONOGENIC DISEASE WITH WIDE RANGE OF SYMPTOMS: DEFICIENCY OF ADENOSINE DEAMINASE 2
Annual European Congress of Rheumatology (EULAR), Madrid, İspanya, 12 - 15 Haziran 2019, cilt.78, ss.1748
OLIGOARTICULAR JUVENILE IDIOPATHIC ARTHRITIS DOES NOT SHOW SIGNS OF T-CELL EXHAUSTION, IN SPITE OF INCREASED EXPRESSION OF CO-INHIBITORY RECEPTORS
Annual European Congress of Rheumatology (EULAR), Madrid, İspanya, 12 - 15 Haziran 2019, cilt.78, ss.151
THE INVESTIGATION OF THE RELATIONSHIP BETWEEN PSYCHOSOCIAL AND FUNCTIONAL STATUS OF CHILDREN WITH JIA
Annual European Congress of Rheumatology (EULAR), Madrid, İspanya, 12 - 15 Haziran 2019, cilt.78, ss.1059-1060
IMPAIRED PLATELET FUNCTIONS IN PATIENTS TREATED WITH COLCHICINE
Annual European Congress of Rheumatology (EULAR), Madrid, İspanya, 12 - 15 Haziran 2019, cilt.78, ss.557-558
IDENTIFYING CANDIDATE ITEMS TOWARDS THE DEVELOPMENT OF CLASSIFICATION CRITERIA FOR CHRONIC NONBACTERIAL OSTEOMYELITIS (CNO) AND CHRONIC RECURRENT MULTIFOCAL OSTEOMYELITIS (CRMO)
Annual European Congress of Rheumatology (EULAR), Madrid, İspanya, 12 - 15 Haziran 2019, cilt.78, ss.254
VALIDATION OF A NOVEL DISEASE CLASSIFICATION IN HACETTEPE TAKAYASU ARTERITIS COHORT
Annual European Congress of Rheumatology (EULAR), Madrid, İspanya, 12 - 15 Haziran 2019, cilt.78, ss.1192
THE CHARACTERISTICS OF PEDIATRIC BEHCET'S DISEASE IN TURKEY VERSUS ISRAEL
Annual European Congress of Rheumatology (EULAR), Madrid, İspanya, 12 - 15 Haziran 2019, cilt.78, ss.424
PEDIATRIC BEHCET'S DISEASE WITH SINUS VENOUS THROMBOSIS: THREE CENTER EXPERIENCE FROM TURKEY
Annual European Congress of Rheumatology (EULAR), Madrid, İspanya, 12 - 15 Haziran 2019, cilt.78, ss.1945-1946
CHOROIDAL EVALUATION IN PATIENTS WITH CHILDHOOD POLYARTERITIS NODOSA (PAN) ANDADENOSINE DEAMINASE-2 DEFICIENCY (DADA-2)
Annual European Congress of Rheumatology (EULAR), Madrid, İspanya, 12 - 15 Haziran 2019, cilt.78, ss.1199
MAY CANCER RISK BE DECREASED IN A LARGE COHORT OF CHILD AND ADULT FAMILIAL MEDITERRANEAN FEVER PATIENTS?
Annual European Congress of Rheumatology (EULAR), Madrid, İspanya, 12 - 15 Haziran 2019, cilt.78, ss.993
THE CHALLENGE OF TREATING PULMONARY VASCULITIS IN BEHCET'S DISEASE: TWO PEDIATRIC CASES
Annual European Congress of Rheumatology (EULAR), Madrid, İspanya, 12 - 15 Haziran 2019, cilt.78, ss.1335-1336
COMORBIDITIES IN FAMILIAL MEDITERRANEAN FEVER
Annual European Congress of Rheumatology (EULAR), Madrid, İspanya, 12 - 15 Haziran 2019, cilt.78, ss.1963
COMPARISON OF THE REASONS FOR NOT GOING TO SCHOOL BETWEEN CHILDREN WITH JUVENILE IDIOPATHIC ARTHRITIS AND THEIR FAMILIES
Annual European Congress of Rheumatology (EULAR), Madrid, İspanya, 12 - 15 Haziran 2019, cilt.78, ss.216-217
SECONDARY VASCULITIS DUE TO SINGLE GENE DEFECTS
19th International Vasculitis and ANCA Workshop, Pennsylvania, Amerika Birleşik Devletleri, 7 - 10 Nisan 2019, cilt.58
PEDIATRIC TO ADULT RHEUMATOLOGY CARE TRANSITION PROGRAMME OF HACETTEPE UNIVERSITY: VASCULITIDES PERSPECTIVE
19th International Vasculitis and ANCA Workshop, Pennsylvania, Amerika Birleşik Devletleri, 7 - 10 Nisan 2019, cilt.58
ARE CHILDHOOD-ONSET AND ADULT-ONSET TAKAYASU ARTERITIS SIMILAR IN TERMS OF CLINICAL FEATURES AND DISEASE COURSE?
19th International Vasculitis and ANCA Workshop, Pennsylvania, Amerika Birleşik Devletleri, 7 - 10 Nisan 2019, cilt.58, ss.63
Farber disease (acid ceramidase deficiency): Data from an ongoing natural history study
15th Annual Research Meeting of the WORLDSymposium(TM), Florida, Amerika Birleşik Devletleri, 4 - 07 Şubat 2019, cilt.126
A REFRACTORY CLINICAL CASE OF LUPUS NEPHRITHIS WHO UNDERWENT BONE MARROW TRANSPLANTATION,
European Society for Paediatric Nephrology, 51th Annual Meeting, 3 - 06 Ekim 2018
FREQUENCY OF THORACOLUMBAR SPINE INVOLVEMENT IN PATIENTS WITH JUVENILE IDIOPATHIC ARTHRITIS
25th Pediatric Rheumatology European Society Congress/Young Investigator Meeting, 5 - 08 Eylül 2018, cilt.16
Oral Health in Children with Familial Mediterranean Fever
CED-IADR/NOF Oral Health Research Congress, Vienna, Avusturya, 21 - 23 Eylül 2017
DIFFERENCES IN PERCEPTION OF THE DISEASE CONSTRAINTS BETWEEN THE CHILD AND PARENTS IN JIA
Annual European Congress of Rheumatology, Madrid, İspanya, 14 - 17 Haziran 2017, cilt.76, ss.1515
TWO-YEAR RESULTS OF A PROSPECTIVE VASCULITIS COHORT FROM EASTERN MEDITERRANEAN: DEMOGRAPHIC CHARACTERISTICS AND DISTRIBUTION OF THE VASCULITIDES FREQUENCIES
18th International Vasculitis and ANCA Workshop, Tokyo, Japonya, 25 - 28 Mart 2017, cilt.56
Type I interferon associated immune responses In STING associated vasculopathy with onset in infancy (SAVI) patients
International Congress of Immunology (ICI), Melbourne, Avustralya, 21 - 26 Ağustos 2016, cilt.46, ss.904
INVESTIGATION OF INTERACTION BETWEEN HAND DEXTERITY AND PARENTAL ATTITUDE IN CHILDREN WITH JUVENILE IDIOPATHIC ARTHRITIS
Annual European Congress of Rheumatology (EULAR), London, Kanada, 8 - 11 Haziran 2016, cilt.75, ss.1265
Farber disease: Implications of anti-inflammatory treatment
12th Annual WORLD Symposium, California, Amerika Birleşik Devletleri, 29 Şubat - 04 Mart 2016, cilt.117
Farber disease is characterized by typical features but a broad phenotypic spectrum: Selected information from a cohort of 37 patients
12th Annual WORLD Symposium, California, Amerika Birleşik Devletleri, 29 Şubat - 04 Mart 2016, cilt.117
Inflammatory milieu of muscle biopsies and clinical features in juvenile dermatomyositis
20th International Congress of the World-Muscle-Society, Brighton, Birleşik Krallık, 30 Eylül - 04 Ekim 2015, cilt.25
Genome Wide Association Meta-Analysis Implicates HLA-DRB1, The BTNL2/HLA-DRA region, and a Novel Susceptibility Locus On Chromosome 1 In Systemic Juvenile Idiopathic Arthritis
77th Annual Meeting of the American-College-of-Rheumatology / 48th Annual Meeting of the Association-of-Rheumatology-Health-Professionals, California, Amerika Birleşik Devletleri, 25 - 30 Ekim 2013, cilt.65
CONVERSION TO SIROLIMUS IN PEDIATRIC RENAL TRANSPLANT RECIPIENTS
50th European-Renal-Association - European-Dialysis-and-Transplant-Association Congress, İstanbul, Türkiye, 18 - 21 Mayıs 2013, cilt.28, ss.294
Results From a Multicentre International Registry of Familial Mediterranean Fever: Impact of Genetic and Environment Factors On the Expression of a Monogenic Disease in Children
Annual Scientific Meeting of the American-College-of-Rheumatology (ACR) and Association-of-Rheumatology-Health-Professionals (ARHP), Washington, Kiribati, 9 - 14 Kasım 2012, cilt.64
Genome-Wide Association Meta-Analysis of Eight Independent Systemic Juvenile Idiopathic Arthritis Collections Reveals Regional Association Spanning the Major Histocompatibility Complex Class II and III Gene Cluster
Annual Scientific Meeting of the American-College-of-Rheumatology (ACR) and Association-of-Rheumatology-Health-Professionals (ARHP), Washington, Kiribati, 9 - 14 Kasım 2012, cilt.64
Major Histocompatibility Complex Class II Gene Cluster Harbors Systemic Juvenile Idiopathic Arthritis Susceptibility Locus
75th Annual Scientific Meeting of the American-College-of-Rheumatology/46th Annual Scientific Meeting of the Association-of-Rheumatology-Health-Professionals, Illinois, Amerika Birleşik Devletleri, 4 - 09 Kasım 2011, cilt.63
Eye involvement in children with primary FSGS
44th ERA-EDTA Congress, Barcelona, İspanya, 22 - 24 Haziran 2007, cilt.22, ss.292
Molecular basis of cystinosis in Turkish patients
44th ERA-EDTA Congress, Barcelona, İspanya, 22 - 24 Haziran 2007, cilt.22, ss.30-31
Influence of monocyte chemoattractant protein-1-2518A > G polymorphism on childhood focal segmental glomerulosclerosis
43rd ERA-EDTA Congress, Glasgow, Birleşik Krallık, 15 - 18 Temmuz 2006, cilt.21, ss.328
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