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Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 11/2015, Volume 125, Issue 11, pp. 4196 - 4211
Journal Article
Arthritis & Rheumatology, ISSN 2326-5191, 08/2016, Volume 68, Issue 8, pp. 2044 - 2049
Objective To investigate the molecular cause of persistent fevers in a patient returning from working overseas, in whom investigations for tropical diseases... 
Sequence Deletion | Humans | Fever - genetics | Adult | Male | Mosaicism | Receptors, Tumor Necrosis Factor, Type I - genetics | Hereditary Autoinflammatory Diseases - genetics | Gangrene | Tumor necrosis factor-TNF | Sperm | Rodents
Journal Article
Annals of the Rheumatic Diseases, ISSN 0003-4967, 04/2019, Volume 78, Issue 4, pp. 571 - 573
Correspondence to Dr Despina Eleftheriou, Infection, Inflammation and Rheumatology Section, UCL Great Ormond Street Institute of Child Health, London, UK;... 
autoinflammation | hypereosinophilia | MEFV | pyrin | PROTEIN | RHEUMATOLOGY | PYRIN | Phosphorylation | Serine | Childrens health | Leukocytes (mononuclear) | Leukocytes (neutrophilic) | Heredity | Grants | Patients | Fever | Lipopolysaccharides | Proteins | 14-3-3 protein | Hospitals | Transfection | Pyrin protein | Biopsy | Cell lines | Peripheral blood mononuclear cells | Skin diseases | Ligands | Mutation | Chemokines | Binding sites | Letter | 2311 | 1506
Journal Article
PLoS ONE, ISSN 1932-6203, 07/2017, Volume 12, Issue 7, p. e0181874
Journal Article
Pediatrics, ISSN 0031-4005, 01/2017, Volume 139, Issue 1, pp. e1 - e1
Juvenile systemic lupus erythematosus (jSLE) is rare before 5 years of age. Monogenic causes are suspected in cases of very early onset jSLE particularly in... 
Journal Article
Pediatrics, ISSN 0031-4005, 01/2017, Volume 139, Issue 1, p. e1
  Juvenile systemic lupus erythematosus (jSLE) is rare before 5 years of age. Monogenic causes are suspected in cases of very early onset jSLE particularly in... 
Lupus | Proteins | Medical treatment | Mutation | Medical diagnosis
Journal Article
Brain, ISSN 0006-8950, 03/2019, Volume 142, Issue 3, pp. e8 - e8
Journal Article
Rheumatology (Oxford, England), ISSN 1462-0324, 08/2019
Hereditary systemic autoinflammatory diseases are rare genetic disorders, which if untreated, can be complicated by AA amyloidosis leading to renal failure and... 
Journal Article
PEDIATRIC RHEUMATOLOGY, ISSN 1546-0096, 07/2019, Volume 17, Issue 1, pp. 39 - 7
BackgroundDeficiency of adenosine deaminase 2 (DADA2) is a rare autosomal recessive autoinflammatory condition. Recognised features include vasculitis... 
DIAGNOSIS | Aspirin | Biomarker | MANAGEMENT | DADA2 | PHENOTYPE | RHEUMATOLOGY | MICROPARTICLES | STROKE | Testicular infarction | ENDOTHELIAL INJURY | REPAIR | Vasculitis | PEDIATRICS | Anti-tumour necrosis factor alpha | POLYARTERITIS-NODOSA | MUTATIONS | Deficiency of adenosine deaminase 2 | Child | Case studies | Genetic disorders | Diagnosis | Ischemia | Pediatric research
Journal Article
Journal Article
JCR: Journal of Clinical Rheumatology, ISSN 1076-1608, 10/2018, p. 1
Journal Article
JCR: Journal of Clinical Rheumatology, ISSN 1076-1608, 10/2018, p. 1
Journal Article
PLoS ONE, ISSN 1932-6203, 10/2012, Volume 7, Issue 10, p. e47673
Journal Article