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
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
Journal Article
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
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
Journal Article
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 | 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
UVEITIS | EMBOLISM | PEDIATRICS | ARTERY ANEURYSMS | OUTCOME SURVEY | INVOLVEMENT | 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
Journal Article
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
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
Journal Article
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
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
Journal Article
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
INTERLEUKIN-1 RECEPTOR ANTAGONIST | RHEUMATOLOGY
Journal Article
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
Pleural effusion | Kawasaki disease | Pulmonary involvement
Journal Article
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...
Journal Article
Current rheumatology reviews, 2019, Volume 15, Issue 1, p. 14
In the last decade, we have come to better understand and manage the vasculitides. The classification of vasculitides has been revised. Genome- wide...
Journal Article
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
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
Journal Article
Rheumatology, ISSN 1462-0324, 03/2019, Volume 58, Issue Supplement_2
Journal Article
Rheumatology, ISSN 1462-0324, 03/2019, Volume 58, Issue Supplement_2
Journal Article
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
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
Journal Article
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
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
Journal Article
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
Familial Mediterranean fever | Severity | Medicine & Public Health | Adherence to colchicine | Rheumatology | DRUG | VALIDATION | RHEUMATOLOGY | ADHERENCE
Journal Article
16.
Paediatric Behçet's disease with sinus venous thrombosis: experience from three centres from Turkey
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...
Journal Article
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
pathogenesis | treatment | pathways | DADA2 | Systemic vasculitis | genetic studies | Adenosine | Genomes | Vasculitis | Adenosine deaminase | Pathogenesis | Haploinsufficiency
Journal Article
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
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
Journal Article
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
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
Journal Article
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
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
Journal Article
No results were found for your search.
Cannot display more than 1000 results, please narrow the terms of your search.