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1. Full Text Mean platelet volume in children with familial Mediterranean fever
by Makay, Balahan and Türkyilmaz, Zeynep and Ünsal, Erbil
Clinical Rheumatology, ISSN 0770-3198, 2009, Volume 28, Issue 8, pp. 975 - 978
Familial Mediterranean fever (FMF) is the most common inherited periodic fever syndrome characterized by recurrent episodes of serositis. Recently, a few... 
Mean platelet volume | Familial Mediterranean fever | Children | Atherosclerosis | INTIMA-MEDIA THICKNESS | ACTIVATION | COLCHICINE | MARKERS | RHEUMATOLOGY | INTERLEUKIN-6 | Severity of Illness Index | Colchicine - therapeutic use | Humans | Male | Blood Platelets - physiology | Familial Mediterranean Fever - drug therapy | Case-Control Studies | Tubulin Modulators - therapeutic use | Familial Mediterranean Fever - blood | Platelet Count | Platelet Activation | Female | C-Reactive Protein - analysis | Child | Genetic aspects | Medical examination | Colchicine | Blood | Drug therapy
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2. Full Text The relationship of neutrophil-to-lymphocyte ratio with gastrointestinal bleeding in Henoch–Schonlein purpura
by Makay, Balahan and Gücenmez, Özge Altuğ and Duman, Murat and Ünsal, Erbil
Rheumatology International, ISSN 0172-8172, 9/2014, Volume 34, Issue 9, pp. 1323 - 1327
Henoch–Schönlein purpura (HSP) is the most common systemic vasculitis of childhood. Gastrointestinal (GI) bleeding is one of the major complications of HSP.... 
Medicine & Public Health | Neutrophil-to-lymphocyte ratio | Gastrointestinal bleeding | Rheumatology | Henoch–Schönlein purpura | Henoch-Schönlein purpura | Henoch-Schonlein purpura | OUTCOMES | RHEUMATOLOGY | ASSOCIATION | CHILDHOOD | CHILDREN | Lymphocyte Count | Mean Platelet Volume | Leukocyte Count | Purpura, Schoenlein-Henoch - physiopathology | Humans | Purpura (Pathology) | Hemoglobin | Heat shock proteins | Lymphocytes | Analysis
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3. Current information about vaccination practice in pediatric rheumatic diseases and recommendations for future applications
by Açarı, Ceyhun and Ünsal, Erbil
Turkish Journal of Pediatrics, ISSN 0041-4301, 2017, Volume 59, Issue 4, pp. 357 - 368
Pediatric patients with autoinflammatory or rheumatic diseases are at increased risk of infections; therefore, safe and effective immunizations are crucial in... 
Live-atenuated vaccine | Pediatric rheumatic disease | Vaccination | Biologicals | SYSTEMIC-LUPUS-ERYTHEMATOSUS | ANTI-TNF | IMMUNIZATION PRACTICES ACIP | JUVENILE IDIOPATHIC ARTHRITIS | pediatric rheumatic disease | biologicals | ADVISORY-COMMITTEE | INFLAMMATORY-BOWEL-DISEASE | PNEUMOCOCCAL POLYSACCHARIDE VACCINE | HEPATITIS-B VACCINATION | IMMUNE-RESPONSES | PEDIATRICS | live-atenuated vaccine | CLINICAL-PRACTICE | vaccination | Immunocompromised Host - immunology | Rheumatic Diseases - drug therapy | Vaccination - methods | Humans | Immunosuppressive Agents - therapeutic use | Immunosuppressive Agents - adverse effects | Vaccination - adverse effects | Child | Practice Guidelines as Topic | Rheumatic Diseases - immunology
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4. Full Text Cardiac autonomic functions in children with familial Mediterranean fever
by Şahin, Murat and Şahin, Murat and Kır, Mustafa and Kır, Mustafa and Makay, Balahan and Makay, Balahan and Keskinoğlu, Pembe and Keskinoğlu, Pembe and Bora, Elçin and Bora, Elçin and Ünsal, Erbil and Ünsal, Erbil and Ünal, Nurettin and Ünal, Nurettin
Clinical Rheumatology, ISSN 0770-3198, 5/2016, Volume 35, Issue 5, pp. 1237 - 1244
Familial Mediterranean fever (FMF) is the most common inherited autoinflammatory disease in the world. The long-term effects of subclinical inflammation in FMF... 
Head upright tilt test | Familial Mediterranean fever | Medicine & Public Health | Autonomic Function | Rheumatology | RHEUMATOID-ARTHRITIS | DIAGNOSIS | SYSTEMIC-LUPUS-ERYTHEMATOSUS | RHEUMATOLOGY | IMPAIRMENT | COLCHICINE | FIBROMYALGIA | AMYLOIDOSIS | QT DISPERSION | DYSFUNCTION | PITUITARY-ADRENAL AXIS | Heart - physiopathology | Cross-Sectional Studies | Humans | Familial Mediterranean Fever - complications | Male | Primary Dysautonomias - physiopathology | Autonomic Nervous System - physiopathology | Primary Dysautonomias - complications | Familial Mediterranean Fever - physiopathology | Adolescent | Electrocardiography | Heart Rate - physiology | Female | Blood Pressure - physiology | Child | Electrocardiography, Ambulatory | Genetic aspects | Heart beat | Electrocardiogram
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5. Full Text Response to: Mean platelet volume and neutrophil-to-lymphocyte ratio in patients with Henoch–Schonlein purpura
by Makay, Balahan and Gücenmez, Özge Altuğ and Duman, Murat and Ünsal, Erbil
Rheumatology International, ISSN 0172-8172, 9/2014, Volume 34, Issue 9, pp. 1337 - 1337
Medicine & Public Health | Rheumatology | RHEUMATOLOGY | Lymphocyte Count | Mean Platelet Volume | Leukocyte Count | Purpura, Schoenlein-Henoch - physiopathology | Humans | Lymphocytes | Emergency medicine
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6. Full Text Performance of Current Guidelines for Diagnosis of Macrophage Activation Syndrome Complicating Systemic Juvenile Idiopathic Arthritis
by Davì, Sergio and Minoia, Francesca and Pistorio, Angela and Horne, AnnaCarin and Consolaro, Alessandro and Rosina, Silvia and Bovis, Francesca and Cimaz, Rolando and Gamir, Maria Luz and Ilowite, Norman T and Kone‐Paut, Isabelle and Feitosa de Oliveira, Sheila Knupp and McCurdy, Deborah and Silva, Clovis Artur and Sztajnbok, Flavio and Tsitsami, Elena and Unsal, Erbil and Weiss, Jennifer E and Wulffraat, Nico and Abinun, Mario and Aggarwal, Amita and Apaz, Maria Teresa and Astigarraga, Itziar and Corona, Fabrizia and Cuttica, Ruben and D'Angelo, Gianfranco and Eisenstein, Eli M and Hashad, Soad and Lepore, Loredana and Mulaosmanovic, Velma and Nielsen, Susan and Prahalad, Sampath and Rigante, Donato and Stanevicha, Valda and Sterba, Gary and Susic, Gordana and Takei, Syuji and Trauzeddel, Ralf and Zletni, Mabruka and Ruperto, Nicolino and Martini, Alberto and Cron, Randy Q and Ravelli, Angelo and Pediat Rheumatology Collaborative and Childhood Arthritis Rheumatology R and Paediat Rheumatology Int Trials Or and Histiocyte Soc and Paediatric Rheumatology International Trials Organisation, the Childhood Arthritis and Rheumatology Research Alliance, the Pediatric Rheumatology Collaborative Study Group, and the Histiocyte Society
Arthritis & Rheumatology, ISSN 2326-5191, 10/2014, Volume 66, Issue 10, pp. 2871 - 2880
Objective To compare the capacity of the 2004 diagnostic guidelines for hemophagocytic lymphohistiocytosis (HLH‐2004) with the capacity of the preliminary... 
DISEASE | INDICATOR | DISORDERS | RATIO | AGREEMENT | RHEUMATOLOGY | HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS | CHILDREN | Macrophage Activation Syndrome - diagnosis | Diagnosis, Differential | Humans | Child, Preschool | Lymphohistiocytosis, Hemophagocytic - diagnosis | Infant | Macrophage Activation Syndrome - complications | Male | Arthritis, Juvenile - complications | Female | Retrospective Studies | In Vitro Techniques | Child | Practice Guidelines as Topic
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7. Full Text Response to: Predictive role of neutrophil-to-lymphocyte ratio in Henoch–Schonlein purpura-related gastrointestinal bleeding
by Makay, Balahan and Gücenmez, Özge Altuğ and Duman, Murat and Ünsal, Erbil
Rheumatology International, ISSN 0172-8172, 9/2014, Volume 34, Issue 9, pp. 1333 - 1333
Medicine & Public Health | Rheumatology | RHEUMATOLOGY | Gastrointestinal Hemorrhage - immunology | Lymphocytes - immunology | Humans | Neutrophils - immunology | Female | Male | Purpura, Schoenlein-Henoch - immunology | Lymphocytes | Emergency medicine
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8. Using biologic agents in pediatric rheumatologic diseases
by Unsal, Erbil
Anti-Inflammatory and Anti-Allergy Agents in Medicinal Chemistry, ISSN 1871-5230, 03/2010, Volume 9, Issue 1, pp. 41 - 45
Juvenile Idiopathic Arthritis (JIA) is an 'umbrella' term which is used to cover Juvenile Rheumatoid Arthritis (JRA) and Juvenile Chronic Arthritis (JCA).... 
Treatment | Biologic agents | Juvenile idiopathic arthritis
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9. Full Text Depression and anxiety in children and adolescents with familial Mediterranean fever
by Makay, Balahan and Makay, Balahan and Emiroğlu, Neslihan and Emiroğlu, Neslihan and Ünsal, Erbil and Ünsal, Erbil
Clinical Rheumatology, ISSN 0770-3198, 4/2010, Volume 29, Issue 4, pp. 375 - 379
Familial Mediterranean fever (FMF) is the most common autoinflammatory disease which requires a lifelong treatment. The aim of this study was to evaluate the... 
Medicine & Public Health | Rheumatology | Depression | Anxiety | Familial Mediterranean fever | Children | Adolescents | COLCHICINE | AMYLOIDOSIS | RISK | QUALITY-OF-LIFE | HEALTH | EPILEPSY | RHEUMATOLOGY | Depression - etiology | Humans | Adolescent | Familial Mediterranean Fever - psychology | Familial Mediterranean Fever - complications | Female | Male | Child | Anxiety - etiology | Case-Control Studies | Psychological aspects | Depression, Mental | Genetic aspects | Child psychopathology
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10. Evaluation of restless legs syndrome and growing pains in children with familial mediterranean fever
by Altuğ-Gücenmez, Özge and Makay, Balahan and Kaçar, Ayla and Ünsal, Erbil
Turkish Journal of Pediatrics, ISSN 0041-4301, 2018, Volume 60, Issue 2, pp. 159 - 164
Growing pains (GP) and restless leg syndrome (RLS) are one of the frequently seen pain syndromes of childhood. These two pain syndromes -GP and RLS-may be... 
Restless legs syndrome | Exertional leg pain | Growing pains | Familial mediterranean fever | CRITERIA | DIAGNOSIS | DISEASES | growing pains | restless legs syndrome | PEDIATRICS | familial Mediterranean fever
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11. Full Text Phagocyte-specific S100 proteins and high-sensitivity C reactive protein as biomarkers for a risk-adapted treatment to maintain remission in juvenile idiopathic arthritis: a comparative study
by Gerss, Joachim and Roth, Johannes and Holzinger, Dirk and Ruperto, Nicolino and Wittkowski, Helmut and Frosch, Michael and Wulffraat, Nico and Wedderburn, Lucy and Stanevicha, Valda and Mihaylova, Dimitrina and Harjacek, Miroslav and Len, Claudio and Toppino, Claudia and Masi, Massimo and Minden, Kirsten and Saurenmann, Traudel and Uziel, Yosef and Vesely, Richard and Apaz, Maria Teresa and Kuester, Rolf-Michael and Elorduy, Maria Jesus Rua and Burgos-Vargas, Ruben and Ioseliani, Maka and Magni-Manzoni, Silvia and Unsal, Erbil and Anton, Jordi and Balogh, Zsolt and Hagelberg, Stefan and Mazur-Zielinska, Henryka and Tauber, Tsivia and Martini, Alberto and Foell, Dirk and Paediat Rheumatology Int Trials and Paediatric Rheumatology International Trials Organization (PRINTO) and for the Paediatric Rheumatology International Trials Organization (PRINTO)
Annals of the Rheumatic Diseases, ISSN 0003-4967, 12/2012, Volume 71, Issue 12, pp. 1991 - 1997
Objectives Juvenile idiopathic arthritis (JIA) is a chronic inflammatory joint disease affecting children. Even if remission is successfully induced, about... 
CLINICAL REMISSION | RHEUMATOID-ARTHRITIS | CRITERIA | NEUTROPHIL ACTIVATION | DISEASE | SELECT CATEGORIES | RHEUMATOLOGY | Biomarkers - metabolism | Recurrence | Calgranulin B - metabolism | Calgranulin A - metabolism | Humans | Leukocyte L1 Antigen Complex - metabolism | Risk Factors | Kaplan-Meier Estimate | Male | S100 Proteins - metabolism | Drug Monitoring - methods | Phagocytes - metabolism | Remission Induction | Arthritis, Juvenile - drug therapy | Arthritis, Juvenile - metabolism | S100A12 Protein | C-Reactive Protein - metabolism | Sensitivity and Specificity | ATP-Binding Cassette Transporters - metabolism | Female | Arthritis, Juvenile - epidemiology | Child | Antirheumatic Agents - therapeutic use | Control | Care and treatment | C-reactive protein | Juvenile arthritis | Physiological aspects | Inflammation | Research | Diagnosis | Biological markers | Health aspects | Immune system | Proteins | Immunology | Statistical analysis | Cytokines | Granulocytes | Laboratories | Bowel disease | Neutrophils | Biomarkers | Arthritis | Patients
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12. Full Text Development and initial validation of the MS score for diagnosis of macrophage activation syndrome in systemic juvenile idiopathic arthritis
by Minoia, Francesca and Bovis, Francesca and Davì, Sergio and Horne, AnnaCarin and Fischbach, Michel and Frosch, Michael and Huber, Adam and Jelusic, Marija and Sawhney, Sujata and McCurdy, Deborah K and Silva, Clóvis A and Rigante, Donato and Unsal, Erbil and Ruperto, Nicolino and Martini, Alberto and Cron, Randy Q and Ravelli, Angelo and Childhood Arthritis Rheumatolog and Histiocyte Soc and Pediat Rheumatology Int Trials Org and Pediat Rheumatology Collabora and Pediatric Rheumatology International Trials Organization, the Childhood Arthritis & Rheumatology Research Alliance, the Pediatric Rheumatology Collaborative Study Group and the Histiocyte Society
Annals of the Rheumatic Diseases, ISSN 0003-4967, 10/2019, Volume 78, Issue 10, pp. 1357 - 1362
ObjectiveTo develop and validate a diagnostic score that aids in identifying macrophage activation syndrome (MAS) in patients with systemic juvenile idiopathic... 
GUIDELINES | RHEUMATOLOGY | FEATURES
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13. Full Text Canakinumab in patients with systemic juvenile idiopathic arthritis and active systemic features: results from the 5-year long-term extension of the phase III pivotal trials
by Ruperto, Nicolino and Brunner, Hermine I and Quartier, Pierre and Constantin, Tamàs and Wulffraat, Nico M and Horneff, Gerd and Kasapcopur, Ozgur and Schneider, Rayfel and Anton, Jordi and Barash, Judith and Berner, Reinhard and Corona, Fabrizia and Cuttica, Ruben and Fouillet-desjonqueres, Marine and Fischbach, Michel and Foster, Helen E and Foell, Dirk and Radominski, Sebastião C and Ramanan, Athimalaipet V and Trauzeddel, Ralf and Unsal, Erbil and Levy, Jérémy and Vritzali, Eleni and Martini, Alberto and Lovell, Daniel J and Paediat Rheumatology Int Trials and PRCSG and Paediatric Rheumatology International Trials Organisation (PRINTO) and the Pediatric Rheumatology Collaborative Study Group (PRCSG) and On behalf of the Paediatric Rheumatology International Trials Organisation (PRINTO) and the Pediatric Rheumatology Collaborative Study Group (PRCSG)
Annals of the Rheumatic Diseases, ISSN 0003-4967, 12/2018, Volume 77, Issue 12, pp. 1710 - 1719
ObjectivesTo evaluate the long-term efficacy and safety of canakinumab in patients with active systemic juvenile idiopathic arthritis (JIA).MethodsPatients... 
clinical trial | systemic juvenile idiopathic arthritis | canakinumab | long-term extension | interleukin-1β | CRITERIA | EFFICACY | SAFETY | MACROPHAGE ACTIVATION SYNDROME | DOUBLE-BLIND | PRELIMINARY DEFINITION | PLACEBO-CONTROLLED TRIAL | SELECT CATEGORIES | RHEUMATOLOGY | DISEASE-ACTIVITY | CHILDREN | Pediatrics | Glucocorticoids | Pathogenesis | Rheumatology | Clinical trials | Arthritis | Macrophages | Patients | Cell activation | Collaboration | Questionnaires | Rheumatism | TNF inhibitors | Remission | Safety | Drug dosages | Clinical and Epidemiological Research | 2311 | 1506
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14. Full Text Does breast-feeding affect severity of familial Mediterranean fever?
by Makay, Balahan and Ünsal, Erbil
Clinical Rheumatology, ISSN 0770-3198, 12/2009, Volume 28, Issue 12, pp. 1389 - 1393
Familial Mediterranean fever (FMF) is the most common inherited autoinflammatory disease, which is caused by an inborn error in innate immune system. It was... 
Disease severity | Breast-feeding | Innate immunity | Familial Mediterranean fever | PROTECTION | GUT | CHILDHOOD LEUKEMIA | RHEUMATOLOGY | MEFV-GENE | CHILDREN | HUMAN-MILK | RISK-FACTOR | AMYLOIDOSIS | DISEASE | Severity of Illness Index | Cytoskeletal Proteins - genetics | Humans | Breast Feeding | Familial Mediterranean Fever - genetics | Child, Preschool | Familial Mediterranean Fever - complications | Male | Pyrin | Young Adult | Erythema - etiology | Familial Mediterranean Fever - physiopathology | Time Factors | DNA Mutational Analysis | Adolescent | Arthritis - etiology | Female | Surveys and Questionnaires | Amyloidosis - etiology | Mutation | Child | Genetic aspects | Breast feeding | Cattle | Medical research | Breastfeeding & lactation | Immune system
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15. Full Text EULAR/PRINTO/PRES criteria for Henoch-Schönlein purpura, childhood polyarteritis nodosa, childhood Wegener granulomatosis and childhood Takayasu arteritis: Ankara 2008. Part I: Overall methodology and clinical characterisation
by Ruperto, Nicolino and Ozen, Seza and Pistorio, Angela and Dolezalova, Pavla and Brogan, Paul and Cabral, David A and Cuttica, Ruben and Khubchandani, Raju and Lovell, Daniel J and O'Neil, Kathleen M and Quartier, Pierre and Ravelli, Angelo and Iusan, Silvia M and Filocamo, Giovanni and Magalhães, Claudia Saad and Unsal, Erbil and Oliveira, Sheila and Bracaglia, Claudia and Bagga, Arvind and Stanevicha, Valda and Manzoni, Silvia Magni and Pratsidou, Polyxeni and Lepore, Loredana and Espada, Graciela and Paut, Isabelle Kone and Zulian, Francesco and Barone, Patrizia and Bircan, Zelal and Maldonado, Maria del Rocio and Russo, Ricardo and Vilca, Iris and Tullus, Kjell and Cimaz, Rolando and Horneff, Gerd and Anton, Jordi and Garay, Stella and Nielsen, Susan and Barbano, Giancarlo and Martini, Alberto and PRINTO and Paediatric Rheumatology International Trials Organisation (PRINTO) and for the Paediatric Rheumatology International Trials Organisation (PRINTO)
Annals of the Rheumatic Diseases, ISSN 0003-4967, 05/2010, Volume 69, Issue 5, pp. 790 - 797
Objectives To report methodology and overall clinical, laboratory and radiographic characteristics for Henoch–Schönlein purpura (HSP), childhood polyarteritis... 
JUVENILE DERMATOMYOSITIS | SYSTEMIC-LUPUS-ERYTHEMATOSUS | PROSPECTIVE VALIDATION | COLLEGE | INTERNATIONAL CONSENSUS | PRELIMINARY DEFINITION | CLASSIFICATION | RHEUMATOLOGY | RHEUMATOLOGY 1990 CRITERIA | ACTIVITY CORE SET | DISEASE-ACTIVITY | Granulomatosis with Polyangiitis - diagnosis | Polyarteritis Nodosa - diagnosis | Takayasu Arteritis - diagnosis | Reproducibility of Results | Humans | International Cooperation | Purpura, Schoenlein-Henoch - diagnosis | Purpura, Schoenlein-Henoch - classification | Takayasu Arteritis - classification | Delphi Technique | Biopsy | Adolescent | Granulomatosis with Polyangiitis - classification | Internet | Polyarteritis Nodosa - classification | Child | Studies | Datasets | Nephrology | Kawasaki disease | Working groups | Physicians | Laboratories | Classification | Rheumatology | Data collection | Adults | Agreements
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16. Full Text Correction to: Evaluation of the effects of miRNAs in familial Mediterranean fever
by Hortu, Hacer Orsdemir and Karaca, Emin and Sozeri, Betul and Gulez, Nesrin and Makay, Balahan and Gunduz, Cumhur and Atik, Tahir and Tekin, Ismihan Merve and Unsal, Sevket Erbil and Cogulu, Ozgur
Clinical rheumatology, ISSN 0770-3198, 03/2019, Volume 38, Issue 3, pp. 645 - 645
The name of the last author of this article was incorrectly presented as "Cogulu Ozgur" this should have been "Ozgur Cogulu". 
Medicine, Experimental | Medical research | Genetic aspects | MicroRNA | Analysis | Medical genetics | Familial Mediterranean fever
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17. Paediatric Behçet's disease with sinus venous thrombosis: experience from three centres from Turkey
by Demir, Selcan and Acari, Ceyhun and Basaran, Ozge and Sağ, Erdal and Karlı Oğuz, Kader and Bilginer, Yelda and Ünsal, Sevket Erbil and Özen, Seza
Clinical and experimental rheumatology, ISSN 0392-856X, 07/2019
To report our experiences of the juvenile Behçet's disease (BD) patients with cerebral venous sinus thrombosis (CVST) and to review previous studies reporting... 
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18. Full Text Mean platelet volume in Henoch-Schönlein purpura: Relationship to gastrointestinal bleeding
by Makay, Balahan and Türkyñlmaz, Zeynep and Duman, Murat and Ünsal, Erbil
Clinical Rheumatology, ISSN 0770-3198, 2009, Volume 28, Issue 10, pp. 1225 - 1228
Henoch-Schonlein purpura (HSP) is the most common systemic vasculitis in children. Gastrointestinal (GI) bleeding is one of the major complications affecting... 
Mean platelet volume | Henoch-Schönlein purpura | Gastrointestinal bleeding | CRITERIA | MARKER | CLASSIFICATION | Henoch-Schonlein purpura | RHEUMATOLOGY | INTERLEUKIN-6 | THROMBOPOIETIN | CHILDHOOD | CHILDREN | INFLAMMATORY-BOWEL-DISEASE | THROMBOCYTOSIS | Predictive Value of Tests | Humans | Risk Factors | Child, Preschool | Male | Gastrointestinal Hemorrhage - epidemiology | Case-Control Studies | C-Reactive Protein - metabolism | Platelet Count | Purpura, Schoenlein-Henoch - complications | Female | Purpura, Schoenlein-Henoch - blood | Leukocyte Count | Retrospective Studies | Child | Purpura (Pathology) | Heat shock proteins | Medical research
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