A5065451290- Inflammasome and immune disorders
- Autoimmune and Inflammatory Disorders Research
- Adolescent and Pediatric Healthcare
- Gout, Hyperuricemia, Uric Acid
- Eosinophilic Esophagitis
- Systemic Lupus Erythematosus Research
- Osteomyelitis and Bone Disorders Research
- Renal Diseases and Glomerulopathies
- Rheumatoid Arthritis Research and Therapies
- Myasthenia Gravis and Thymoma
- Venous Thromboembolism Diagnosis and Management
- IL-33, ST2, and ILC Pathways
- Streptococcal Infections and Treatments
- Pulmonary Hypertension Research and Treatments
- Cholesterol and Lipid Metabolism
- Omental and Epiploic Conditions
- Children's Physical and Motor Development
- Salivary Gland Tumors Diagnosis and Treatment
- Dermatological and COVID-19 studies
- Poisoning and overdose treatments
- Vascular Malformations and Hemangiomas
- Elbow and Forearm Trauma Treatment
- interferon and immune responses
- Nuclear Issues and Defense
- Kawasaki Disease and Coronary Complications
Gazi University
2021-2025
Mersin Üniversitesi
2025
Abstract Juvenile idiopathic arthritis (JIA) presents with diverse phenotypes and can lead to significant morbidity. Obesity, affecting 5 23% of JIA patients, may exacerbate disease activity complicate management. This study evaluates the impact body mass index (BMI) on influence joint involvement BMI in patients. Between January 2012 June 2024, 225 patients were reviewed, 173 ultimately included based specific inclusion exclusion criteria. Treatments followed American College Rheumatology...
Abstract Background Juvenile idiopathic arthritis (JIA) is a prevalent childhood chronic arthritis, often persisting into adulthood. Effective transitional care becomes crucial as these patients transition from pediatric to adult healthcare systems. Despite the concept of being recognized, its real-world implementation remains inadequately explored. This study aims evaluate thoughts and practices providers regarding for JIA patients. Methods A cross-sectional survey was conducted among...
The exact effects of MEFV variants on inflammation are still under investigation, and reports unknown significance, particularly the E148Q variant, have been conflicting. Therefore, this study aims to investigate patients exhibiting heterozygosity, focusing diagnoses disease courses assist physicians in interpreting variant.
Persistent inflammation is an insidious feature of familial Mediterranean fever (FMF) that may cause chronic complications. This study aimed to investigate the predictors persistent in children with FMF.The medical charts 1077 paediatric FMF patients were retrospectively collected. The divided into two groups: and without subclinical inflammation.A total 133 (12%) had inflammation. M694V homozygosity, colchicine resistance, positive family history for FMF, erysipelas-like erythema, leg pain,...
Familial Mediterranean fever (FMF) is an autoinflammatory disease which may cause endothelial dysfunction and arterial stiffness. In this study, we evaluated patients with FMF in terms of stiffness indicators investigated whether there was any difference according to colchicine response. This a single-center, prospective, case-control study conducted on pediatric FMF. Patients were categorized into 2 groups: monotherapy (group 1) who used anti-interleukin-1 (IL-1) plus 2). Patient age,...
Background. Familial Mediterranean fever (FMF) is the most common and autosomal recessive inherited autoinflammatory disease. The signs symptoms are fever, abdominal pain, chest arthritis. aim of this study was to describe clinical, laboratory genetic differences between pediatric FMF patients with without pain. Methods. Between January 2006 2022, 1134 were analyzed retrospectively. Patients divided into two groups including those recurrent These compared in demographic, treatment, MEFV gene...
Abstract Thymic tumors are very rare neoplasms in children and account for less than 1% of mediastinal pediatric patients. One‐third the patients present with symptoms related to compression tumor mass on surrounding anatomic structures, paraneoplastic syndromes such as myasthenia gravis, pure red cell aplasia, acquired hypogammaglobulinemia, connective tissue disorders, which rarely occur thymic tumors. Herein, we report a case carcinoma mimicking disease symmetrical polyarthritis...
Juvenile idiopathic arthritis (JIA) is a common chronic rheumatic disease in children, requiring careful management to reduce both short- and long-term morbidity. In this study, our objective was assess the clinical features of patients diagnosed with JIA who received intra-articular corticosteroid injections (IACI).
The field of transitional care for chronic conditions in adolescents, notably juvenile idiopathic arthritis (JIA), is rapidly growing. Transitioning these patients to adult healthcare systems presents significant challenges practical implementation. Consequently, it would be appropriate each country develop a transition program tailored its specific infrastructure. To pursue this goal, Delphi study was conducted identify the key components JIA. Three panels and two rounds were held...
Journal Article Corrected proof Giant thymic cyst overclouding the diagnosis of fibrodysplasia ossificans progressiva: an inconvenient coincidence Get access Batuhan Küçükali, Küçükali Department Pediatric Rheumatology, Gazi University Faculty Medicine, Ankara, Turkey Correspondence to: Emniyet, Mevlana Blv. No: 29, Besevler, Ankara 06500, Turkey. E-mail: batuhankucukali@gmail.com https://orcid.org/0000-0002-4268-8603 Search for other works by this author on: Oxford Academic PubMed Google...
OBJECTIVES: The aim of the study was to compare hippocampus sizes healthy medical faculty students, who were exposed an intense data input and underwent serious learning activity those sport students did sports regularly by using MR images examine relationship between a size intelligence.METHODS: We made with 58 young males (27 sciences 31 students).R. B. Cattell 3A Culture Fair Intelligence Test administered volunteers.Following this, we got our volunteers.RESULTS: could not fi nd...
Giriş: Tularemi, gram-negatif Francisella tularensis'ten kaynaklanan oldukça bulaşıcı bakteriyel zoonotik bir hastalıktır.Hastalık klinisyenler için zordur ve nadir görülmesi nedeniyle tanı yüksek düzeyde şüphe gerekir.Bu çalışmanın amacı, kliniğimizde tedavi edilen pediatrik
InvestigationÖz Giriş: Tularemi, gram-negatif Francisella tularensis'ten kaynaklanan oldukça bulaşıcı bakteriyel zoonotik bir hastalıktır.Hastalık klinisyenler için zordur ve nadir görülmesi nedeniyle tanı yüksek düzeyde şüphe gerekir.Bu çalışmanın amacı, kliniğimizde tedavi edilen pediatrik