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index medicus (14) 14
rheumatology (12) 12
pediatrics (11) 11
children (10) 10
familial mediterranean fever (10) 10
arthritis (8) 8
diagnosis (8) 8
humans (7) 7
child (6) 6
patients (6) 6
adolescent (5) 5
vasculitis (5) 5
classification (4) 4
criteria (4) 4
fever (4) 4
inflammation (4) 4
male (4) 4
medicine & public health (4) 4
analysis (3) 3
colchicine (3) 3
disease (3) 3
female (3) 3
juvenile idiopathic arthritis (3) 3
management (3) 3
mutation (3) 3
rheumatoid-arthritis (3) 3
age (2) 2
anakinra (2) 2
antigens (2) 2
association (2) 2
autoimmune diseases (2) 2
behcet syndrome - drug therapy (2) 2
care and treatment (2) 2
child, preschool (2) 2
children & youth (2) 2
classification criteria (2) 2
colchicine - therapeutic use (2) 2
cytokines (2) 2
familial mediterranean fever - diagnosis (2) 2
familial mediterranean fever - drug therapy (2) 2
gastric carcinoma (2) 2
henoch-schonlein purpura (2) 2
interferon (2) 2
interleukin 1 (2) 2
kawasaki disease (2) 2
krukenberg tumour (2) 2
medical research (2) 2
medicine (2) 2
medicine, experimental (2) 2
nodular lesions on the skin (2) 2
outcome survey (2) 2
pain (2) 2
psoriasis (2) 2
research (2) 2
retrospective studies (2) 2
treatment (2) 2
treatment outcome (2) 2
validation (2) 2
abdomen (1) 1
abo (1) 1
abo system (1) 1
abridged index medicus (1) 1
acquired immune deficiency syndrome--aids (1) 1
adenosine (1) 1
adenosine deaminase (1) 1
adherence (1) 1
adherence to colchicine (1) 1
adolescent mothers (1) 1
adolescents (1) 1
adults (1) 1
age factors (1) 1
age groups (1) 1
allergic rhinitis (1) 1
amyloidosis (1) 1
aneurysms (1) 1
anti-il-1 treatment (1) 1
antibodies, monoclonal - therapeutic use (1) 1
anxiety (1) 1
armenian patients (1) 1
artery aneurysms (1) 1
arthritis, juvenile - complications (1) 1
arthritis, juvenile - diagnosis (1) 1
arthritis, juvenile - drug therapy (1) 1
articles (1) 1
auto-inflammatory syndromes (1) 1
autoimmunity (1) 1
autoinflammatory diseases (1) 1
azathioprine (1) 1
behcet disease (1) 1
behcet syndrome - complications (1) 1
behcet syndrome - diagnosis (1) 1
behcet syndrome - diagnostic imaging (1) 1
behcet's disease (1) 1
behcet's syndrome (1) 1
behcets-disease (1) 1
biologic drugs (1) 1
biopsy (1) 1
biopsychosocial (1) 1
blends:polymer (1) 1
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1. Full Text Development of Novel Nano-ZnO Enhanced Polymeric Membranes for Water Purification
by Taha, Attallah K. T and Amir, Md and Demir Korkmaz, Ayse and Al-Messiere, Munirah Abdullah and Baykal, Abdulhadi and Karakuş, Selcan and Kilislioglu, Ayben
Journal of Inorganic and Organometallic Polymers and Materials, ISSN 1574-1443, 2018, Volume 29, Issue 3, pp. 979 - 988
ZnO nanoparticles (NPs) were treated using three different polymers: polysulfone (PSF), polyvinylpyrrolidone (PVP), and polyvinylidene fluoride (PVDF). 10wt%... 
Sonication | Polyvinylidene fluoride | Polysulfones | ZnO nanoparticles | Water purification | Nanocomposite membrane | ROOM-TEMPERATURE | POLYMER SCIENCE | PERFORMANCE | PVP | PVDF | NANOPARTICLES | GAS PERMEATION | REMOVAL | FTIR | FABRICATION | NANOCOMPOSITE | Povidone | Water | Purification | Analysis | Resveratrol | Zinc oxide | Fluorine compounds | Polymer industry
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2. Monogenic Periodic Fever Syndromes: Treatment Options for the Pediatric Patient
by Ozen, Seza and Demir, Selcan
Pediatric Drugs, ISSN 1174-5878, 08/2017, Volume 19, Issue 4, pp. 303 - 311
Autoinflammatory diseases are disorders of the innate immune system characterized by uncontrolled inflammation. The most commonly encountered autoinflammatory... 
FAMILIAL MEDITERRANEAN FEVER | SYNDROME TRAPS | BONE-MARROW-TRANSPLANTATION | TNF-RECEPTOR | PEDIATRICS | PHARMACOLOGY & PHARMACY | MUCKLE-WELLS-SYNDROME | OPEN-LABEL | COLD AUTOINFLAMMATORY SYNDROME | HYPERIMMUNOGLOBULINEMIA D SYNDROME | OF-THE-LITERATURE | LONG-TERM EFFICACY
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3. Monogenic Periodic Fever Syndromes: Treatment Options for the Pediatric Patient
by Ozen, Seza and Demir, Selcan
Paediatric drugs, 08/2017, Volume 19, Issue 4, p. 303
Autoinflammatory diseases are disorders of the innate immune system characterized by uncontrolled inflammation. The most commonly encountered autoinflammatory... 
Colchicine - therapeutic use | Humans | Fever - diagnosis | Antibodies, Monoclonal - therapeutic use | Treatment Outcome | Familial Mediterranean Fever - drug therapy | Hereditary Autoinflammatory Diseases - diagnosis | Cryopyrin-Associated Periodic Syndromes - drug therapy | Mevalonate Kinase Deficiency - drug therapy | Hereditary Autoinflammatory Diseases - drug therapy | Mevalonate Kinase Deficiency - diagnosis | Cryopyrin-Associated Periodic Syndromes - diagnosis | Interleukin-1 - immunology | Familial Mediterranean Fever - diagnosis | Interleukin-1 - antagonists & inhibitors | Child | Fever - drug therapy
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4. Full Text Anakinra treatment in macrophage activation syndrome: a single center experience and systemic review of literature
by Sönmez, Hafize Emine and Demir, Selcan and Bilginer, Yelda and Özen, Seza
Clinical Rheumatology, ISSN 0770-3198, 12/2018, Volume 37, Issue 12, pp. 3329 - 3335
Our aim was to report our experiences of pediatric macrophage activation syndrome (MAS) patients treated with anakinra and to review previous studies reporting... 
Medicine & Public Health | Anakinra | Rheumatology | Auto-inflammatory syndromes | Juvenile idiopathic arthritis | Macrophage activation syndrome | RHEUMATOID-ARTHRITIS | DIAGNOSIS | MULTICENTER | MUTATION | DISEASE | RHEUMATOLOGY | HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS | FEVER | Autoimmunity | Macrophage Activation Syndrome - drug therapy | Humans | Child, Preschool | Infant | Macrophage Activation Syndrome - complications | Male | Treatment Outcome | Inflammation | Remission Induction | Arthritis, Juvenile - drug therapy | Interleukin 1 Receptor Antagonist Protein - therapeutic use | Adolescent | Arthritis, Juvenile - complications | Patient Safety | Female | Child | Medicine, Experimental | Medical research | Arthritis | Macrophages | Literature reviews | Pediatrics | Cell activation | Acquired immune deficiency syndrome--AIDS | Interleukin 1 receptor antagonist | Interleukin 1 | Remission | Patients
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5. Full Text The Challenge of Treating Pulmonary Vasculitis in Behcet Disease: Two Pediatric Cases
by Demir, S and Sag, E and Akca, UK and Hazirolan, T and Bilginer, Y and Ozen, S
PEDIATRICS, ISSN 0031-4005, 08/2019, Volume 144, Issue 2, p. e20190162
Behcet disease (BD) is a multisystemic autoinflammatory disorder characterized by recurrent mucocutaneous, ocular, musculoskeletal, gastrointestinal, central... 
UVEITIS | EMBOLISM | PEDIATRICS | ARTERY ANEURYSMS | OUTCOME SURVEY | INVOLVEMENT | Cyclophosphamide - administration & dosage | Behcet Syndrome - diagnostic imaging | Humans | Behcet Syndrome - drug therapy | Male | Lung Diseases - diagnostic imaging | Lung Diseases - drug therapy | Vasculitis - drug therapy | Adolescent | Vasculitis - diagnostic imaging | Drug Therapy, Combination | Immunosuppressive Agents - administration & dosage | Methylprednisolone - administration & dosage | Behcet's syndrome | Pediatrics | Intravenous administration | Mortality | Lung diseases | Central nervous system | Methylprednisolone | Patients | Morbidity | Immunosuppressive agents | Hemoptysis | Cyclophosphamide | Vasculitis | Interferon | Diagnostic systems | Autoimmune diseases | Prednisolone
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6. Full Text Testing the Model for Predicting Effectiveness of Anakinra in Systemic Juvenile Idiopathic Arthritis
by Ozen, S and Demir, S and Batu, ED
JOURNAL OF RHEUMATOLOGY, ISSN 0315-162X, 10/2019, Volume 46, Issue 10, pp. 1422 - 1423
We read the article by Saccomanno, , "Predictors of effectiveness of anakinra in systemic juvenile idiopathic arthritis," with great interest They reported... 
INTERLEUKIN-1 RECEPTOR ANTAGONIST | RHEUMATOLOGY
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7. Full Text Pleural effusion as an atypical presentation of Kawasaki disease: a case report and review of the literature
by Arslanoglu Aydin, Elif and Demir, Selcan and Aydin, Orkun and Bilginer, Yelda and Ozen, Seza
Journal of Medical Case Reports, ISSN 1752-1947, 12/2019, Volume 13, Issue 1, pp. 1 - 6
Abstract Background Kawasaki disease is an acute, febrile vasculitis of childhood that affects medium-sized arteries, predominantly the coronary arteries. It... 
Pleural effusion | Kawasaki disease | Pulmonary involvement
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8. Full Text Performance of the new 'Eurofever/PRINTO classification criteria' in FMF patients
by Sag, Erdal and Demirel, Dilara and Demir, Selcan and Atalay, Erdal and Akca, Ummusen and Bilginer, Yelda and Ozen, Seza
Seminars in arthritis and rheumatism, ISSN 0049-0172, 08/2019
Recently a new set of criteria proposed for the classification of auto inflammatory recurrent fevers including familial Mediterranean Fever (FMF). We aimed to... 
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9. Full Text Familial mediterranean fever: Recent developments in pathogenesis and new recommendations for management
by Özen, Seza and Batu, Ezgi Deniz and Demir, Selcan
Frontiers in Immunology, ISSN 1664-3224, 03/2017, Volume 8, p. 253
Familial Mediterranean fever (FMF) is the most common monogenic autoinflammatory disease (AID) affecting mainly the ethnic groups originating from... 
Familial Mediterranean fever | Rho GTPases | Colchicine | MEFV | Pyrin | DIAGNOSTIC-VALUE | RECEIVING COLCHICINE | PROTRACTED FEBRILE MYALGIA | INFLAMMASOME ACTIVATION | colchicine | ANTI-IL-1 TREATMENT | IMMUNOLOGY | pyrin | MEFV-GENE ANALYSIS | ARMENIAN PATIENTS | familial Mediterranean fever | COLCHICINE-RESISTANT | JAPANESE PATIENTS | GENOTYPE-PHENOTYPE | Care and treatment | Usage | Inflammation | Analysis
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10. Full Text 317. PEDIATRIC TO ADULT RHEUMATOLOGY CARE TRANSITION PROGRAMME OF HACETTEPE UNIVERSITY: VASCULITIDES PERSPECTIVE
by Bolek, Ertugrul Cagri and Demir, Selcan and Sari, Alper and Akca, Ummusen Kaya and Kilic, Levent and Akdogan, Ali and Kiraz, Sedat and Ozen, Seza and Karadag, Omer
Rheumatology, ISSN 1462-0324, 03/2019, Volume 58, Issue Supplement_2
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11. Full Text 146. ARE CHILDHOOD-ONSET AND ADULT-ONSET TAKAYASU ARTERITIS SIMILAR IN TERMS OF CLINICAL FEATURES AND DISEASE COURSE?
by Cagri, Ertugrul and Demir, Bolek Selcan and Sari, Alper and Akca, Ummusen Kaya and Kilic, Levent and Akdogan, Ali and Kiraz, Sedat and Karadag, Omer and Özen, Seza
Rheumatology, ISSN 1462-0324, 03/2019, Volume 58, Issue Supplement_2
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12. Full Text Is age associated with disease severity and compliance to treatment in children with familial Mediterranean fever?
by Sönmez, Hafize Emine and Sönmez, Hafize Emine and Esmeray, Pelin and Esmeray, Pelin and Batu, Ezgi Deniz and Batu, Ezgi Deniz and Arıcı, Zehra Serap and Arıcı, Zehra Serap and Demir, Selcan and Demir, Selcan and Sağ, Erdal and Sağ, Erdal and Özen, Seza and Özen, Seza and Bilginer, Yelda and Bilginer, Yelda
Rheumatology International, ISSN 0172-8172, 1/2019, Volume 39, Issue 1, pp. 83 - 87
Familial Mediterranean Fever (FMF) is the most common monogenic autoinflammatory disease in the world. The disease characteristics may vary in different age... 
Familial Mediterranean fever | Severity | Medicine & Public Health | Adherence to colchicine | Rheumatology | DRUG | VALIDATION | RHEUMATOLOGY | ADHERENCE | Severity of Illness Index | Age Factors | Cross-Sectional Studies | Colchicine - therapeutic use | Humans | Child, Preschool | Male | Familial Mediterranean Fever - drug therapy | Tubulin Modulators - therapeutic use | Medication Adherence | Adolescent | Female | Familial Mediterranean Fever - diagnosis | Child
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13. Full Text The factors affecting the disease course in Kawasaki disease
by Arslanoglu Aydin, Elif and Ertugrul, Ilker and Bilginer, Yelda and Batu, Ezgi Deniz and Sonmez, Hafize Emine and Demir, Selcan and Arici, Zehra Serap and Sag, Erdal and Alehan, Dursun and Ozen, Seza
Rheumatology International, ISSN 0172-8172, 08/2019, Volume 39, Issue 8, pp. 1343 - 1349
The aim of this study was to review the characteristics of patients with Kawasaki disease (KD) from Turkey and to assess the performance of the Kobayashi score... 
Echocardiography | Kawasaki disease | IVIG resistance | Coronary artery aneurysm | Predictive score | DIAGNOSIS | RISK-FACTORS | RESISTANCE | RHEUMATOLOGY | CHILDREN | Medical research | Analysis | Medicine, Experimental | Aneurysms | Study and teaching | College teachers | Cardiology | Blood cell count
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14. Full Text Vasculitis in systemic autoinflammatory diseases
by Demir, Selcan and Sag, Erdal and Dedeoglu, Fatma and Ozen, Seza
Frontiers in Pediatrics, ISSN 2296-2360, 2018, Volume 6, p. 377
Autoinflammatory diseases (AID) are diseases of the innate immune system, characterized by recurrent episodes of localized or systemic inflammation. Vasculitis... 
Autoinflammatory diseases | Relopathies | Vasculitis | Behcet disease | Interferonopathies | Inflammasomopathies | interferonopathies | vasculitis | PERIODIC SYNDROME | autoinflammatory diseases | NLRP3 INFLAMMASOME ACTIVATION | inflammasomopathies | BEHCETS-DISEASE | OUTCOME SURVEY | MEFV GENE-MUTATIONS | FAMILIAL MEDITERRANEAN FEVER | HENOCH-SCHONLEIN PURPURA | HYPERIMMUNOGLOBULINEMIA-D | PEDIATRICS | relopathies | CLASSIFICATION CRITERIA | GENOME-WIDE ASSOCIATION | Research | Autoimmune diseases | Tumor necrosis factor
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15. Vasculitis: Decade in Review
by Demir, Selcan and Sönmez, Hafize Emine and Özen, Seza
Current rheumatology reviews, ISSN 1573-3971, 2019, Volume 15, Issue 1, pp. 14 - 22
Background: In the last decade, we have come to better understand and manage the vasculitides. The classification of vasculitides has been revised. Genome-... 
pathogenesis | treatment | pathways | DADA2 | Systemic vasculitis | genetic studies | Adenosine | Genomes | Vasculitis | Adenosine deaminase | Pathogenesis | Haploinsufficiency
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16. Full Text Pediatric forms of vasculitis
by Özen, Seza and Sönmez, Hafize Emine and Demir, Selcan
Best Practice & Research Clinical Rheumatology, ISSN 1521-6942, 02/2018, Volume 32, Issue 1, pp. 137 - 147
Primary vasculitides that affect children are a challenging and complex group of disorders that may involve any system of the body and lead to significant... 
Primary vasculitides | Childhood vasculitides | Management | Classification | CHURG-STRAUSS-SYNDROME | TAKAYASU ARTERITIS | CLINICAL-FEATURES | RHEUMATOLOGY | RHEUMATOLOGY 1990 CRITERIA | CHILDHOOD WEGENER GRANULOMATOSIS | ONSET BEHCETS-DISEASE | KAWASAKI-DISEASE | HENOCH-SCHONLEIN PURPURA | POLYARTERITIS-NODOSA | CLASSIFICATION CRITERIA | Vasculitis - classification | Child | Humans | Vasculitis - pathology | Pediatrics | Vasculitis
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17. Full Text A new biopsychosocial and clinical questionnaire to assess juvenile idiopathic arthritis: JAB-Q
by Unal, Edibe and Batu, Ezgi Deniz and Sonmez, Hafize Emine and Arici, Zehra Serap and Arin, Gamze and Karaca, Nur Banu and Sag, Erdal and Demir, Selcan and Hakli, Duygu Aydin and Ozcadirci, Aykut and Oflaz, Fatma Birgul and Alpar, Reha and Bilginer, Yelda and Ozen, Seza
Rheumatology International, ISSN 0172-8172, 8/2018, Volume 38, Issue 8, pp. 1557 - 1564
To create a new multidimensional questionnaire for the assessment of juvenile idiopathic arthritis (JIA) patients in standard clinical practice and study the... 
Biopsychosocial | Medicine & Public Health | Outcome | Rheumatology | Juvenile idiopathic arthritis | RHEUMATOID-ARTHRITIS | PSYCHOMETRIC PROPERTIES | ANXIETY | VALIDATION | RHEUMATOLOGY | DISEASE-ACTIVITY | CHILDREN | OUTCOME MEASURES | PAIN | SCALE | HEALTH-STATUS | Reproducibility of Results | Parents - psychology | Humans | Adolescent | Arthritis, Juvenile - diagnosis | Quality of Life | Female | Male | Retrospective Studies | Child | Surveys and Questionnaires - standards | Surveys | Arthritis | Diagnosis | Validity | Parents & parenting | Questionnaires | Clinical medicine | Patients | Children & youth
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18. Full Text Severe hypersensitivity reactions to biological drugs in children with rheumatic diseases
by Soyer, Ozge and Demir, Selcan and Bilginer, Yelda and Batu, Ezgi Deniz and Sonmez, Hafize Emine and Arıcı, Zehra Serap and Şahiner, Ümit Murat and Sekerel, Bulent Enis and Ozen, Seza and Atanaskovic‐Markovic, Marina
Pediatric Allergy and Immunology, ISSN 0905-6157, 12/2019, Volume 30, Issue 8, pp. 833 - 840
Background Hypersensitivity reactions (HSR) to biologic drugs (BD) may limit their use in children with rheumatic diseases. We aimed to analyze the incidence... 
hypersensitivity | rheumatic diseases | biologic drugs | children
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19. Noninvasive models to predict liver fibrosis in patients with chronic hepatitis B: A study from Turkey
by Korkmaz, Pinar and Demirturk, Nese and Batırel, Ayse and Cem Yardimci, Ahmet and Cagir, Unal and Nemli, Salih Atakan and Korkmaz, Fatime and Akcam, Fusun Zeynep and Barut, Huseyin Sener and Bayrak, Burcu and Karakecili, Faruk and Tarakci, Huseyin and Yulugkural, Zerrin and Yuksel, Esma and Demir, Nazlım Aktug and Ural, Onur and Sumer, Sua and Harman, Rezan and Kadanali, Ayten and Ozturk, Sinan and Akhan, Sila Cetin and Tulek, Necla Eren and Keten, Derya and Sener, Alper and Aygen, Bilgehan and Celikbas, Aysel Kocagul and Karadag, Fatma Yilmaz and Aydin, Gule and Arslan, Eyup and Sacligil, Cahide and Ocal, Gulfem Akengin and Tanoglu, Alpaslan and Ulcay, Asim and Karagoz, Ergenekon and Saltoglu, Nese and Sırmatel, Fatma and Akdeniz, Hayrettin and Aynıoglu, Aynur and Ozel, Selcan Arslan and Caylak, Selmin Dirgen and Celik, Ilhami and Alpay, Yesim and Dursun, Zehra Bestepe and Bekcibasi, Muhammed and Ertem, Gunay Tuncer and Tigli, Arzu and Altunok, Elif Sargin and Avsar, Kemal and Suer, Kaya and Sayan, Murat
Hepatitis Monthly, ISSN 1735-143X, 12/2017, Volume 17, Issue 12
Background: Manynoninvasive methods, including aspartateaminotransaminase (AST)/alanineaminotransaminase (ALT) ratio (AAR), AST-to-platelet ratio index (APRI),... 
Chronic hepatitis B | Liver | Fibrosis | Noninvasive models | TESTS | Chronic Hepatitis B | NEUTROPHIL | MANAGEMENT | BIOPSY | LYMPHOCYTE RATIO | Noninvasive Models | CIRRHOSIS | C VIRUS-INFECTION | COHORT | GASTROENTEROLOGY & HEPATOLOGY | PLATELET RATIO INDEX
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20. Comparison of patients with familial Mediterranean fever accompanied with sacroiliitis and patients with juvenile spondyloarthropathy
by Sonmez, HE and Batu, ED and Demir, S and Bilginer, Y and Ozen, S
CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, ISSN 0392-856X, 2017, Volume 35, Issue 6, pp. S124 - S127
Objective. Familial Mediterranean fever (FMF) is the most common auto-inflammatory disease manifesting with self-limited recurrent febrile attacks and... 
CRITERIA | DIAGNOSIS | sacroiliitis | CLASSIFICATION | RHEUMATOLOGY | CHILDREN | juvenile spondyloarthropathy | AMYLOIDOSIS | GENE | DISEASE | IDIOPATHIC ARTHRITIS | familial Mediterranean fever | ASSOCIATION |