Articles

Search Articles

Advanced search
Help

Catalogue

Articles

Databases

X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (1749) 1749
Book / eBook (201) 201
Publication (138) 138
Newsletter (58) 58
Book Review (46) 46
Newspaper Article (25) 25
Book Chapter (23) 23
Magazine Article (7) 7
Conference Proceeding (5) 5
Government Document (5) 5
Reference (2) 2
Journal / eJournal (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (1102) 1102
index medicus (746) 746
male (469) 469
female (442) 442
familial mediterranean fever (408) 408
periodic fever (398) 398
rheumatology (359) 359
child (311) 311
mutation (301) 301
adult (300) 300
fever (265) 265
pediatrics (247) 247
periodic fever syndrome (217) 217
diagnosis (214) 214
child, preschool (206) 206
immunology (206) 206
adolescent (203) 203
syndrome (202) 202
hyperimmunoglobulinemia-d (195) 195
inflammation (181) 181
mutations (180) 180
children (176) 176
periodicals (168) 168
aphthous stomatitis (165) 165
middle aged (162) 162
anakinra (161) 161
research (158) 158
diagnosis, differential (148) 148
familial mediterranean fever - genetics (144) 144
medicine & public health (138) 138
pharyngitis (137) 137
disease (136) 136
autoinflammatory diseases (134) 134
medicine, general & internal (134) 134
amyloidosis (127) 127
treatment outcome (127) 127
phenotype (126) 126
infant (123) 123
periodic syndrome (123) 123
cryopyrin-associated periodic syndromes - genetics (121) 121
medicine (121) 121
animals (120) 120
analysis (118) 118
care and treatment (118) 118
muckle-wells-syndrome (118) 118
nlr family, pyrin domain-containing 3 protein (114) 114
young adult (114) 114
genetic aspects (109) 109
inflammasome (107) 107
carrier proteins - genetics (105) 105
abridged index medicus (104) 104
familial mediterranean fever - diagnosis (103) 103
pfapa syndrome (102) 102
canakinumab (101) 101
gene (98) 98
autoinflammatory syndromes (97) 97
cryopyrin-associated periodic syndromes - drug therapy (96) 96
hereditary autoinflammatory diseases - genetics (95) 95
receptors, tumor necrosis factor, type i - genetics (94) 94
cryopyrin-associated periodic syndromes (93) 93
internal medicine (92) 92
periodic syndrome traps (91) 91
periodical publishing (91) 91
encoding mevalonate kinase (89) 89
diseases (88) 88
mevalonate kinase-deficiency (88) 88
patients (87) 87
tnf receptor (87) 87
arthritis (85) 85
interleukin-1 (85) 85
hyper-igd syndrome (84) 84
cryopyrin-associated periodic syndromes - diagnosis (83) 83
pyrin (83) 83
risk factors (82) 82
hereditary autoinflammatory diseases - diagnosis (79) 79
health aspects (78) 78
interleukin 1 receptor antagonist protein - therapeutic use (76) 76
dermatology (75) 75
antibodies, monoclonal - therapeutic use (71) 71
cytokines (71) 71
periodic health examinations (71) 71
mevalonate kinase (70) 70
aged (69) 69
clinical neurology (69) 69
colchicine (69) 69
activation (68) 68
cold autoinflammatory syndrome (68) 68
genetics (68) 68
medical research (68) 68
physical diagnosis (68) 68
traps (68) 68
hyper-igd (67) 67
familial mediterranean fever - drug therapy (66) 66
juvenile idiopathic arthritis (66) 66
medicine, research & experimental (65) 65
phosphotransferases - genetics (65) 65
autoinflammatory disease (64) 64
genetics & heredity (64) 64
interleukin-1 receptor antagonist (64) 64
periodicals as topic (64) 64
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (70) 70
Robarts - Stacks (44) 44
UTL at Downsview - May be requested (37) 37
UofT at Mississauga - Stacks (17) 17
St. Michael's College (John M. Kelly) - 2nd Floor (9) 9
UofT at Scarborough - Stacks (9) 9
Collection Dvlpm't (Acquisitions) - Closed Orders (7) 7
Collection Dvlpm't (Acquisitions) - Vendor file (7) 7
OISE - Stacks (6) 6
Sunnybrook Health Sciences Centre - Sunnybrook Stacks (6) 6
Toronto East General Hospital - Stacks (6) 6
Victoria University E.J. Pratt - Reference (5) 5
Victoria University E.J. Pratt - Stacks (5) 5
Credit Valley Hospital - Stacks (4) 4
Faculty of Information - Stacks (4) 4
Gerstein Science - Reference (4) 4
Lakeridge Health Sciences - Oshawa (4) 4
Providence Healthcare - Stacks (4) 4
Robarts - Reference (4) 4
Scarborough Hospital - General (4) 4
St. Michael's Hospital - Stacks (4) 4
Trinity College (John W Graham) - Stacks (4) 4
Humber River Regional Hospital - Finch Stacks (3) 3
Royal Ontario Museum - Stacks (3) 3
Humber River Regional Hospital - Church Stacks (2) 2
Massey College (Robertson Davies) - Rare Book (2) 2
Music - Stacks (2) 2
University College (Laidlaw) - Stacks (2) 2
UofT Schools - Stacks (2) 2
UofT at Mississauga - Reference (2) 2
UofT at Scarborough - Withdrawn (2) 2
Art - Library use only (1) 1
Baycrest Hospital - Stacks (1) 1
Chemistry (A D Allen) - Stacks (1) 1
Credit Valley Hospital - Missing (1) 1
Credit Valley Hospital - Reference (1) 1
Credit Valley Hospital - Special Collections (1) 1
Dentistry (Harry R Abbott) - Stacks (1) 1
Dentistry (Harry R Abbott) - Withdrawn (1) 1
Earth Sciences (Noranda) - Reference (1) 1
Earth Sciences (Noranda) - Stacks (1) 1
Faculty of Information - Subject Analysis Systems (1) 1
Gerstein Science - Course Reserves (1) 1
Gerstein Science - May be requested (1) 1
Gerstein Science - Missing (1) 1
Humber River Regional Hospital - Church Reference (1) 1
Humber River Regional Hospital - Finch Reference (1) 1
Innis College - Reference (1) 1
Knox College (Caven) - Stacks (1) 1
Media Commons - Storage (1) 1
New College (Ivey) - Stacks (1) 1
Not Returned (1) 1
OISE - Curriculum Resources (1) 1
OISE - Reference (1) 1
OISE - Storage (1) 1
Pontifical Inst. Mediaeval Studies - Library use only (1) 1
Pontifical Inst. Mediaeval Studies - Reference (1) 1
Providence Healthcare - Reference (1) 1
Providence Healthcare - Reserve desk (1) 1
Robarts - Government Pubs (1) 1
Robarts - Storage (1) 1
Royal Ontario Museum - Reference (1) 1
Scarborough Hospital - Birchmount (1) 1
Scarborough Hospital - Hospital Department (1) 1
Scarborough Hospital - Stacks (1) 1
St Josephs Health Centre - Stacks (1) 1
St. Michael's College (John M. Kelly) - 3rd Floor (1) 1
St. Michael's Hospital - Sunnybrook Stacks (1) 1
Stacks (1) 1
Sunnybrook Health Sciences Centre - Holland Stacks (1) 1
Sunnybrook Health Sciences Centre - Pharmacy (1) 1
Thomas Fisher Rare Book - Rare Book (1) 1
Toronto East General Hospital - Online (1) 1
Toronto East General Hospital - Reference (1) 1
Trillium Health Centre - Reserve desk (1) 1
Trinity College (John W Graham) - Storage (1) 1
University College (Laidlaw) - Purdy (1) 1
Victoria University CRRS - Library use only (1) 1
Victoria University Emmanuel College - Birge Storage (1) 1
West Park Healthcare Centre - Stacks (1) 1
Women's College Hospital - Stacks (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (1841) 1841
German (73) 73
French (57) 57
Spanish (53) 53
Japanese (15) 15
Russian (11) 11
Portuguese (8) 8
Turkish (8) 8
Italian (7) 7
Korean (4) 4
Arabic (3) 3
Czech (3) 3
Danish (3) 3
Polish (3) 3
Chinese (1) 1
Dutch (1) 1
Estonian (1) 1
Greek (1) 1
Hungarian (1) 1
Slovak (1) 1
Slovenian (1) 1
Swedish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


1. Full Text Periodic fever syndromes
by Lachmann, Helen J
Best Practice and Research: Clinical Rheumatology, ISSN 1521-6942, 08/2017, Volume 31, Issue 4, pp. 596 - 609
Periodic fever syndromes are autoinflammatory diseases. The majority present in infancy or childhood and are characterised by recurrent episodes of fever and... 
Aphthous stomatitis | Pharyngitis and cervical adenitis (PFAPA) | Deficiency of adenosine deaminase 2 (DADA2) | Tumour necrosis factor (TNF) receptor-associated periodic syndrome (TRAPS) | Blau syndrome | Deficiency of IL-1 receptor antagonist (DIRA) | Familial Mediterranean fever (FMF) | Mevalonate kinase deficiency (MKD) | Cryopyrin-associated periodic syndromes (CAPS) | Deficiency of IL-36 receptor antagonist (DITRA) | Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature syndrome (CANDLE) | RECURRENT MULTIFOCAL OSTEOMYELITIS | TNF RECEPTOR | OPEN-LABEL | RHEUMATOLOGY | CONGENITAL DYSERYTHROPOIETIC ANEMIA | FAMILIAL MEDITERRANEAN FEVER | HYPERIMMUNOGLOBULINEMIA-D | CANAKINUMAB TREATMENT | AUTOINFLAMMATORY DISEASES | COLCHICINE-RESISTANT | Colchicine - therapeutic use | Humans | Child, Preschool | Fever - diagnosis | Infant | Familial Mediterranean Fever - drug therapy | Hereditary Autoinflammatory Diseases - diagnosis | Cryopyrin-Associated Periodic Syndromes - drug therapy | Immunity, Innate | Hereditary Autoinflammatory Diseases - drug therapy | Syndrome | Tumor Necrosis Factor-alpha - therapeutic use | Cryopyrin-Associated Periodic Syndromes - diagnosis | Familial Mediterranean Fever - diagnosis | Child | Fever - drug therapy | Autoimmunity | Amyloidosis | Autoantibodies | Colchicine | Biological response modifiers
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
2. Full Text Canakinumab for the Treatment of Autoinflammatory Recurrent Fever Syndromes
by De Benedetti, Fabrizio and Gattorno, Marco and Anton, Jordi and Ben-Chetrit, Eldad and Frenkel, Joost and Hoffman, Hal M and Koné-Paut, Isabelle and Lachmann, Helen J and Ozen, Seza and Simon, Anna and Zeft, Andrew and Calvo Penades, Inmaculada and Moutschen, Michel and Quartier, Pierre and Kasapcopur, Ozgur and Shcherbina, Anna and Hofer, Michael and Hashkes, Philip J and Van der Hilst, Jeroen and Hara, Ryoki and Bujan-Rivas, Segundo and Constantin, Tamas and Gul, Ahmet and Livneh, Avi and Brogan, Paul and Cattalini, Marco and Obici, Laura and Lheritier, Karine and Speziale, Antonio and Junge, Guido
The New England Journal of Medicine, ISSN 0028-4793, 05/2018, Volume 378, Issue 20, pp. 1908 - 1919
The anti–interleukin-1 antibody canakinumab was effective at controlling and preventing recurrence of flares in autoimmune inflammatory diseases: familial... 
MEDICINE, GENERAL & INTERNAL | FAMILIAL MEDITERRANEAN FEVER | INFLAMMATION | HYPERIMMUNOGLOBULINEMIA-D | INTERLEUKIN-1-BETA SECRETION | PHASE-II | OPEN-LABEL | ANAKINRA | COLCHICINE-RESISTANT | PERIODIC SYNDROME TRAPS | AA AMYLOIDOSIS | Double-Blind Method | Humans | Antibodies, Monoclonal - adverse effects | Child, Preschool | Antibodies, Monoclonal - therapeutic use | Male | Familial Mediterranean Fever - drug therapy | Mevalonate Kinase Deficiency - drug therapy | Hereditary Autoinflammatory Diseases - drug therapy | Dose-Response Relationship, Drug | Young Adult | Antibodies, Monoclonal - administration & dosage | Injections, Subcutaneous | Adolescent | Adult | Female | Child | Fever - drug therapy | Interleukin-1beta - antagonists & inhibitors | Prevention | Treatment outcome | Fever in children | Diagnosis | Analysis | Pediatrics | Writers | Cytokines | Internal medicine | Laboratories | Rheumatology | Disease control | Patients | Fever | Medicine | Mevalonate kinase | Infectious diseases | Mevalonic acid | Immunology | Hospitals | Familial Mediterranean fever | Mutation | Colchicine | Drug dosages | University colleges
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
3. Full Text Cryopyrin-associated periodic fever syndrome manifesting as Tolosa-Hunt syndrome
by Höhne, C and Schuh, E and Kümpfel, T and Straube, A
Cephalalgia, ISSN 0333-1024, 12/2016, Volume 36, Issue 14, pp. 1392 - 1396
Background Tolosa-Hunt syndrome (THS) is characterized by unilateral orbital pain, ipsilateral oculomotor paresis and a prompt response to treatment with... 
Tolosa-Hunt syndrome | older age | corticosteroid-responsive orbital pain | cryopyrin-associated periodic fever syndrome | late onset | PAINFUL OPHTHALMOPLEGIA | NEUROLOGIC MANIFESTATIONS | NEUROSCIENCES | CLINICAL NEUROLOGY | Cryopyrin-Associated Periodic Syndromes - diagnostic imaging | Ophthalmoplegia - diagnostic imaging | Diagnosis, Differential | Tolosa-Hunt Syndrome - diagnostic imaging | Fever - complications | Humans | Middle Aged | Male | Ophthalmoplegia - complications | Tolosa-Hunt Syndrome - complications | Fever - diagnostic imaging | Cryopyrin-Associated Periodic Syndromes - complications
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
4. Full Text A clinical review of 105 patients with PFAPA (a periodic fever syndrome)
by Feder, HM and Salazar, JC
Acta Pædiatrica, ISSN 0803-5253, 02/2010, Volume 99, Issue 2, pp. 178 - 184
Aims:  We describe the presentations and clinical outcomes of pediatric patients diagnosed with PFAPA (Periodic Fever, Aphthous lesions, Pharyngitis, and... 
PFAPA | periodic fever | aphthous | Aphthous | Periodic fever | CYCLIC NEUTROPENIA | CERVICAL ADENITIS | APHTHOUS STOMATITIS | RECURRENT FEVER | HEREDITARY AUTOINFLAMMATORY SYNDROMES | CHILDREN | CIMETIDINE | PHARYNGITIS | TONSILLECTOMY | DISEASE | PEDIATRICS | Cimetidine - therapeutic use | Humans | Fever - therapy | Periodicity | Child, Preschool | Male | Histamine H2 Antagonists - therapeutic use | Syndrome | Tonsillectomy | Female | Stomatitis, Aphthous | Pharyngitis | Lymphadenitis
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
5. Full Text Familial Mediterranean fever and related periodic fever syndromes/autoinflammatory diseases
by Savic, Sinisa and Dickie, Laura J and Battellino, Michele and McDermott, Michael F
Current Opinion in Rheumatology, ISSN 1040-8711, 01/2012, Volume 24, Issue 1, pp. 103 - 112
PURPOSE OF REVIEWThe spectrum of periodic fever syndromes (PFS)/autoinflammation diseases is continuously expanding. This review provides an overview of the... 
Inflammasome | Autoinflammation | IL-1 | Periodic fevers | PFAPA SYNDROME | KAPPA-B ACTIVATION | periodic fevers | MEVALONATE KINASE-DEFICIENCY | SUSTAINED RESPONSE | APHTHOUS STOMATITIS | autoinflammation | BLAU-SYNDROME | RHEUMATOLOGY | ADENITIS SYNDROME | SYNDROME TRAPS | HYPER-IGD | inflammasome | TNF-RECEPTOR | Mevalonate Kinase Deficiency - etiology | Familial Mediterranean Fever - etiology | Interleukin-1beta - metabolism | Humans | Caspase 1 - metabolism | Familial Mediterranean Fever - metabolism | Mevalonate Kinase Deficiency - metabolism | Familial Mediterranean Fever - drug therapy | Mevalonate Kinase Deficiency - drug therapy
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
6. Full Text Neurology of the cryopyrin‐associated periodic fever syndrome
by Parker, T and Keddie, S and Kidd, D and Lane, T and Maviki, M and Hawkins, P. N and Lachmann, H. J and Ginsberg, L
European Journal of Neurology, ISSN 1351-5101, 07/2016, Volume 23, Issue 7, pp. 1145 - 1151
Background and purpose The cryopyrin‐associated periodic fever syndrome (CAPS) is an autosomal dominant autoinflammatory disorder caused by mutations in the... 
canakinumab | migraine | hearing impairment | NLRP3 | headache | aseptic meningitis | CAPS | Aseptic meningitis | Headache | Migraine | Canakinumab | Hearing impairment | DISEASES | MUCKLE-WELLS-SYNDROME | COLD AUTOINFLAMMATORY SYNDROME | NEUROSCIENCES | CLINICAL NEUROLOGY | Headache - etiology | Cryopyrin-Associated Periodic Syndromes - genetics | Humans | Middle Aged | Child, Preschool | Infant | Male | Myalgia - etiology | United Kingdom | Young Adult | Hearing Loss, Sensorineural - etiology | Adolescent | Adult | Female | Mutation | Child | Cryopyrin-Associated Periodic Syndromes - complications | Papilledema - etiology | Meningitis | Continuing medical education | Interleukins | Fever
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
7. Musculoskeletal manifestations in hereditary periodic fever syndromes
by Soliani, Martina and Soliani, Martina and Cattalini, Marco and Cattalini, Marco and Vitale, Antonio and Vitale, Antonio and Sota, Jurgen and Sota, Jurgen and Cantarini, Luca and Cantarini, Luca
Clinical and experimental rheumatology, ISSN 0392-856X, 01/2018, Volume 36, Issue 1, pp. 25 - S31
Monogenic autoinflammatory diseases (AIDs) are a group of inflammatory disorders induced by deregulation of the innate immune system and characterised by... 
Hereditary periodic fever syndromes | Autoinflammatory diseases | Arthritis | Differential diagnosis | Musculoskeletal involvement | musculoskeletal involvement | differential diagnosis | ONSET AUTOINFLAMMATORY DISORDERS | MEVALONATE KINASE-DEFICIENCY | PROTRACTED FEBRILE MYALGIA | EXPANDING SPECTRUM | autoinflammatory diseases | RECURRENT ACUTE PERICARDITIS | MUCKLE-WELLS-SYNDROME | RHEUMATOLOGY | arthritis | FAMILIAL MEDITERRANEAN FEVER | SYNDROME TRAPS | HYPERIMMUNOGLOBULINEMIA-D | hereditary periodic fever syndromes | TNFRSF1A GENE | Arthralgia - etiology | Hereditary Autoinflammatory Diseases - complications | Myalgia - physiopathology | Arthritis - physiopathology | Musculoskeletal Diseases - etiology | Humans | Hereditary Autoinflammatory Diseases - physiopathology | Musculoskeletal Diseases - physiopathology | Arthritis - etiology | Myalgia - etiology | Arthralgia - physiopathology
Journal Article
Details down arrow
8. Full Text TLR2/TLR4-dependent exaggerated cytokine production in hyperimmunoglobulinaemia D and periodic fever syndrome
by Stoffels, M and Jongekrijg, J and Remijn, T and Kok, N and Meer, J.W.M. van der and Simon, A
Rheumatology, ISSN 1462-0324, 2015, Volume 54, Issue 2, pp. 363 - 368
OBJECTIVE: The autoinflammatory hyperimmunoglobulinaemia D and periodic fever syndrome (HIDS) is characterized by recurrent episodes of fever and inflammation.... 
hyper-IgD syndrome | anakinra | tocilizumab | periodic fever | mevalonate kinase deficiency | autoinflammatory syndrome | ACTIVATION | MEVALONATE KINASE-DEFICIENCY | CASPASE-1 | RHEUMATOLOGY | INHIBITION | IL-1-BETA RELEASE | INFLAMMATORY ATTACKS | MUTATIONS | Leukocytes, Mononuclear - metabolism | Humans | Middle Aged | Male | Mevalonate Kinase Deficiency - metabolism | RNA, Messenger - metabolism | Case-Control Studies | Toll-Like Receptor 4 - physiology | Toll-Like Receptor 2 - physiology | Lipopolysaccharides - pharmacology | Nod2 Signaling Adaptor Protein - pharmacology | Adult | Female | Antirheumatic Agents - pharmacology | Interleukin 1 Receptor Antagonist Protein - pharmacology | Cytokines - biosynthesis
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
9. When to Suspect Autoinflammatory/Recurrent Fever Syndromes
by Verbsky, James W
Pediatric Clinics of North America, ISSN 0031-3955, 02/2017, Volume 64, Issue 1, pp. 111 - 125
Autoinflammatory disorders are disorders characterized by rash, arthritis, fever, and systemic inflammation. These disorders are caused by mutations in genes... 
Innate immunity | TNF-α | IL-1beta | Autoinflammatory | Fever | RECURRENT MULTIFOCAL OSTEOMYELITIS | TNF-alpha | BLAU-SYNDROME | CONGENITAL DYSERYTHROPOIETIC ANEMIA | PERIODIC SYNDROME TRAPS | RECEPTOR ANTAGONIST | ENCODING MEVALONATE KINASE | FAMILIAL MEDITERRANEAN FEVER | HYPERIMMUNOGLOBULINEMIA-D | PYODERMA-GANGRENOSUM | PEDIATRICS | GRANULOMATOUS ARTHRITIS | Rare Diseases - genetics | Recurrence | Diagnosis, Differential | Rare Diseases - immunology | Humans | Hereditary Autoinflammatory Diseases - immunology | Rare Diseases - diagnosis | Delayed Diagnosis | Hereditary Autoinflammatory Diseases - diagnosis | Immunity, Innate | Syndrome | Rare Diseases - therapy | Diagnostic Errors | Hereditary Autoinflammatory Diseases - therapy | Child | Hereditary Autoinflammatory Diseases - genetics
Journal Article
Details down arrow
10. Full Text Validation of the Auto-Inflammatory Diseases Activity Index (AIDAI) for hereditary recurrent fever syndromes
by Piram, Maryam and Koné-Paut, Isabelle and Lachmann, Helen J and Frenkel, Joost and Ozen, Seza and Kuemmerle-Deschner, Jasmin and Stojanov, Silvia and Simon, Anna and Finetti, Martina and Sormani, Maria Pia and Martini, Alberto and Gattorno, Marco and Ruperto, Nicolino and EUROTRAPS Network and Paediat Rheumatology Int Trials and EUROFEVER Network and EUROFEVER, EUROTRAPS and the Paediatric Rheumatology International Trials Organisation (PRINTO) networks
Annals of the Rheumatic Diseases, ISSN 0003-4967, 12/2014, Volume 73, Issue 12, pp. 2168 - 2173
Objectives To validate the Auto-Inflammatory Diseases Activity Index (AIDAI) in the four major hereditary recurrent fever syndromes (HRFs): familial... 
Disease Activity | Fever Syndromes | Familial Mediterranean Fever | HORIZONTAL LINE | CRITERIA | SYSTEMIC-LUPUS-ERYTHEMATOSUS | VISUAL ANALOG SCALES | IMPROVEMENT | CONSENSUS | PRELIMINARY DEFINITION | AUTOINFLAMMATORY DISEASES | RHEUMATOLOGY | ARTHRITIS | RILONACEPT | Severity of Illness Index | Reproducibility of Results | Prospective Studies | Area Under Curve | Mevalonate Kinase Deficiency - physiopathology | Humans | Male | Hereditary Autoinflammatory Diseases - diagnosis | Fever | Mevalonate Kinase Deficiency - diagnosis | Cryopyrin-Associated Periodic Syndromes - physiopathology | Young Adult | Familial Mediterranean Fever - physiopathology | Cryopyrin-Associated Periodic Syndromes - diagnosis | Adolescent | Hereditary Autoinflammatory Diseases - physiopathology | Adult | Female | ROC Curve | Familial Mediterranean Fever - diagnosis | Child | Cohort Studies | Usage | Relapse | Hereditary autoinflammatory diseases | Clinical trials | Research | Risk factors | Diseases | Diaries | Parents & parenting | Pain | Orphans | Physicians | Pathogenesis | Adults | Clinical medicine | Patients | Clinical and Epidemiological Research | 1506
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
11. Full Text 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
by Federici, Silvia and Vanoni, Federica and Ben-Chetrit, Eldad and Cantarini, Luca and Frenkel, Joost and Goldbach-Mansky, Raphaela and Gul, Ahmet and Hoffman, Hal and Koné-Paut, Isabelle and Kuemmerle-Deschner, Jasmin and Lachmann, Helen J and Martini, Alberto and Obici, Laura and Ozen, Seza and Simon, Anna and Hofer, Michael and Gattorno, Marco and Eurofever Pediat Rheumatology Int and Eurofever and the Pediatric Rheumatology International Trials Organization (PRINTO)
Journal of Rheumatology, ISSN 0315-162X, 2019, Volume 46, Issue 4, pp. 429 - 436
Objective. Provisional evidence-based classification criteria for hereditary periodic fever (HPF) have been recently developed. However, no consensus on how to... 
Classification Criteria | TNF receptor-Associated periodic fever syndromes | Cryopyrinopathies | Mevalonate kinase deficiency | Familial mediterranean fever | DIAGNOSIS | FAMILIAL MEDITERRANEAN FEVER | CRYOPYRINOPATHIES | TNF RECEPTOR-ASSOCIATED PERIODIC FEVER SYNDROMES | RHEUMATOLOGY | MEVALONATE KINASE DEFICIENCY | CLASSIFICATION CRITERIA
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
12. Full Text A Comprehensive Overview of the Hereditary Periodic Fever Syndromes
by Rigante, Donato and Frediani, Bruno and Cantarini, Luca
Clinical Reviews in Allergy & Immunology, ISSN 1080-0549, 6/2018, Volume 54, Issue 3, pp. 446 - 453
Innate immunity is a critical partner in the regulation of inflammation and some mutations in genes implied in innate immunity pathways can cause genetic... 
Allergology | Hereditary periodic fever syndromes | Interleukin-1 | Immunology | Medicine & Public Health | Autoinflammation | Internal Medicine | Inflammation | MEVALONATE KINASE-DEFICIENCY | RECURRENT FEVER | CANAKINUMAB | CINCA SYNDROME | OPEN-LABEL | ANAKINRA | IMMUNOLOGY | FAMILIAL MEDITERRANEAN FEVER | GENE | ALLERGY | AUTOINFLAMMATORY DISORDERS | MUTATIONS | Proteins | Physiological aspects | Genetic aspects | B cells | Interleukins | Genes | Interleukin | Disorders | Innate immunity | Antagonists | Biosynthesis | Immunity | Mevalonate kinase | Mevalonic acid | Interleukin 1 | Familial Mediterranean fever | Differential diagnosis | Phenotypes | Cryopyrin | Heredity | Gene expression | Patients | Cholesterol | Fever | Hereditary diseases | Membrane proteins | Signaling | Pyrin protein | Cytoskeleton | Membrane trafficking | Diagnostic systems | Clinical medicine | Mutation | Metabolic disorders | Apoptosis
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
13. Full Text Cytokine signatures in hereditary fever syndromes (HFS)
by Ibrahim, José Noel and Jéru, Isabelle and Lecron, Jean-Claude and Medlej-Hashim, Myrna
Cytokine and Growth Factor Reviews, ISSN 1359-6101, 2016, Volume 33, pp. 19 - 34
Highlights • The current review presents all available data regarding the cytokines’ signatures in HFS at the transcriptional, serum and ex vivo levels. • It... 
Advanced Basic Science | Transcript | Serum | Cytokines | ex vivo | PBMC | Hereditary fever syndromes | MEVALONATE KINASE-DEFICIENCY | INTERLEUKIN-1 RECEPTOR ANTAGONIST | BIOCHEMISTRY & MOLECULAR BIOLOGY | NLRP3 INFLAMMASOME ACTIVATION | CASPASE-1 AUTOPROTEOLYSIS | PERIODIC SYNDROME TRAPS | BLOOD MONONUCLEAR-CELLS | CELL BIOLOGY | RICH REPEAT DOMAIN | FAMILIAL MEDITERRANEAN FEVER | HYPERIMMUNOGLOBULINEMIA-D | AUTOINFLAMMATORY DISEASES | Inflammation | Genetic aspects
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights