| Q40347278 | A 21 year-old woman with fever, arthralgia and leucocitosis |
| Q40640510 | A case of hyperimmunoglobulinemia d syndrome successfully treated with canakinumab |
| Q40579117 | A case of periodic fever... |
| Q40424602 | A case of periodic-fever-syndrome-like disorder with lipodystrophy, myositis, and autoimmune abnormalities. |
| Q81597429 | A case of recurrent pancreatitis due to hyperlipidemia misdiagnosed as familial Mediterranean fever |
| Q48261335 | A comparison of neurodegeneration linked with neuroinflammation in different brain areas of rats after intracerebroventricular colchicine injection |
| Q35638094 | A decision tree for genetic diagnosis of hereditary periodic fever in unselected patients |
| Q62658646 | A fatal turkish case of CINCA-NOMID syndrome due to the novel Val-351-Leu CIAS1 gene mutation |
| Q40565375 | A founder effect in the hyperimmunoglobulinemia D and periodic fever syndrome |
| Q35823352 | A novel tumour necrosis factor receptor mutation in a Finnish family with periodic fever syndrome |
| Q40537418 | A patient with hyper-IgD syndrome in Antalya, Turkey |
| Q27687429 | A preliminary score for the assessment of disease activity in hereditary recurrent fevers: results from the AIDAI (Auto-Inflammatory Diseases Activity Index) Consensus Conference. |
| Q35612400 | Abdominal and digestive system associations of familial Mediterranean fever |
| Q36017329 | Abdominal pain, arthritis, and nephrotic syndrome in a Syrian patient |
| Q37380279 | Abnormal IgD and IgA1 O-glycosylation in hyperimmunoglobulinaemia D and periodic fever syndrome |
| Q40376443 | Adult-onset Still's disease, Schnitzler syndrome, and autoinflammatory syndromes in adulthood |
| Q40215842 | Amyloid A amyloidosis in a Japanese patient with familial Mediterranean fever associated with homozygosity for the pyrin variant M694I/M694I. |
| Q28277791 | Approach to genetic analysis in the diagnosis of hereditary autoinflammatory syndromes |
| Q42375802 | Approach to recurrent fever in childhood |
| Q40573796 | Association of mutations in the NALP3/CIAS1/PYPAF1 gene with a broad phenotype including recurrent fever, cold sensitivity, sensorineural deafness, and AA amyloidosis |
| Q38085854 | Autoinflammation: From monogenic syndromes to common skin diseases |
| Q37128189 | Autoinflammatory diseases: an update of clinical and genetic aspects |
| Q36922302 | Autoinflammatory syndromes with a dermatological perspective |
| Q40407800 | B cell cytopenia in two brothers with hyper-IgD and periodic fever syndrome |
| Q40563606 | Carrier frequency of the V377I (1129G>A) MVK mutation, associated with Hyper-IgD and periodic fever syndrome, in the Netherlands |
| Q39751626 | Colchicinoids from Colchicum crocifolium Boiss. (Colchicaceae). |
| Q39806185 | Common Familial Mediterranean Fever gene mutations in a Turkish cohort |
| Q24337040 | De novo CIAS1 mutations, cytokine activation, and evidence for genetic heterogeneity in patients with neonatal-onset multisystem inflammatory disease (NOMID): a new member of the expanding family of pyrin-associated autoinflammatory diseases |
| Q40480551 | Diagnostic challenge of hyper-IgD syndrome in four children with inflammatory gastrointestinal complaints. |
| Q38046118 | Differential diagnosis and management of Behçet syndrome |
| Q40471156 | Dramatic etanercept-induced remission of relapsing febrile sciatic neuralgia related to p46l mutation of the tnfrsf1a gene. |
| Q40527538 | Effect of inflammatory attacks in the classical type hyper-IgD syndrome on immunoglobulin D, cholesterol and parameters of the acute phase response |
| Q57301721 | Endoscopic findings in patients with familial Mediterranean fever and dyspeptic symptoms |
| Q40289364 | Establishment of a transgenic mouse model with liver-specific expression of secretory immunoglobulin D. |
| Q40110286 | Evaluation of IL-1β, IL-1ra, and IL-10 levels and outcome of periodontal therapy in chronic periodontitis with familial Mediterranean fever |
| Q40261345 | Evaluation of hearing in patients with familial Mediterranean fever |
| Q36112547 | Evaluation of the Mean Platelet Volume and Red Cell Distribution Width in FMF: Are They Related to Subclinical Inflammation or Not? |
| Q34657952 | Falling into TRAPS--receptor misfolding in the TNF receptor 1-associated periodic fever syndrome |
| Q33622298 | Familial Mediterranean Fever developing in a Japanese kidney transplant recipient |
| Q40499439 | Familial Mediterranean fever among the autoimmune diseases |
| Q46555625 | Familial Mediterranean fever protracted febrile myalgia in children: report of two cases |
| Q53649569 | Familial Mediterranean fever. |
| Q33785849 | Familial Mediterranean fever: An unusual disease enlightening the inflammation biology |
| Q38151758 | Familial mediterranean fever: a fascinating model of inherited autoinflammatory disorder |
| Q33186164 | Fever of unknown origin in adults: 40 years on. |
| Q26777200 | Fever tree revisited: From malaria to autoinflammatory diseases |
| Q40499431 | From familial Mediterranean fever to amyloidosis |
| Q95591345 | Gastrointestinal pain |
| Q40062818 | Genetic Analysis of Southwestern Iranian Patients with Familial Mediterranean Fever |
| Q35019675 | Genetic clues to understanding periodic fevers, and possible therapies |
| Q36958310 | Genetics and new treatment modalities for familial Mediterranean fever |
| Q30436426 | Henoch-Schönlein purpura in a child with hyperimmunoglobulinemia D and periodic fever syndrome |
| Q40521835 | Hereditary intermittant fever |
| Q40530243 | Hereditary periodic fever |
| Q24329184 | Heterogeneity among patients with tumor necrosis factor receptor-associated periodic syndrome phenotypes |
| Q40078299 | Hyper-IgD and periodic fever syndrome (HIDS) due to compound heterozygosity for G336S and V377I in a 44-year-old patient with a 27-year history of fever |
| Q37738109 | Hyperimmunoglobulin D syndrome in childhood |
| Q30311123 | Hyperimmunoglobulinemia D and periodic fever syndrome (HIDS) in a child with normal serum IgD, but increased serum IgA concentration |
| Q45240653 | Hyperimmunoglobulinemia D syndrome in an Arab child |
| Q39790268 | INFEVERS: the Registry for FMF and hereditary inflammatory disorders mutations |
| Q42428341 | Identification and functional characterization of a presqualene diphosphate phosphatase |
| Q40516800 | Identification of a novel mevalonate kinase gene mutation in combination with the common MVK V377I substitution and the low-penetrance TNFRSF1A R92Q mutation |
| Q34994477 | Immunodeficiency and genetic conditions that cause arthritis in childhood |
| Q39270778 | In vitro analysis of the functional effects of an NLRP3 G809S variant with the co-existence of MEFV haplotype variants in atypical autoinflammatory syndrome |
| Q41457693 | Inflammatory arthritis in caspase 1 gene-deficient mice: contribution of proteinase 3 to caspase 1-independent production of bioactive interleukin-1beta |
| Q57369432 | Inherited disorders of cholesterol biosynthesis |
| Q26771260 | Innovative Target Therapies Are Able to Block the Inflammation Associated with Dysfunction of the Cholesterol Biosynthesis Pathway |
| Q40229798 | Intermittent neutropenia as an early feature of mild mevalonate kinase deficiency |
| Q55031386 | Is triglyceride/HDL ratio a reliable screening test for assessment of atherosclerotic risk in patients with chronic inflammatory disease? |
| Q78374003 | Juvenile rheumatoid arthritis |
| Q40572763 | Lack of isoprenoid products raises ex vivo interleukin-1beta secretion in hyperimmunoglobulinemia D and periodic fever syndrome |
| Q40579122 | Long live springtime! My mother...it is not a trap... |
| Q40426715 | Lovastatin inhibits formation of AA amyloid |
| Q34567791 | Mevalonate kinase deficiencies: from mevalonic aciduria to hyperimmunoglobulinemia D syndrome |
| Q54385298 | Mevalonate kinase gene mutations and their clinical correlations in Behçet's disease. |
| Q46592108 | Mevalonate metabolism governs cancer immune surveillance. |
| Q58030608 | Molecular Mechanisms of Amyloidosis |
| Q40414781 | Molecular analysis of MEFV gene mutations among Palestinian patients with Behcet's disease |
| Q27687277 | New insights into the enigma of immunoglobulin D. |
| Q24613164 | New mutations of CIAS1 that are responsible for Muckle-Wells syndrome and familial cold urticaria: a novel mutation underlies both syndromes |
| Q40277829 | Novel mutations causing hyperimmunoglobulin D and periodic fever syndrome |
| Q43080349 | Novel polyisoprenyl phosphates block phospholipase D and human neutrophil activation in vitro and murine peritoneal inflammation in vivo |
| Q38122566 | Novel therapeutics for the treatment of familial Mediterranean fever: from colchicine to biologics |
| Q37572943 | Nummular keratopathy in a patient with Hyper-IgD Syndrome |
| Q36822703 | Observational Study of a French and Belgian Multicenter Cohort of 23 Patients Diagnosed in Adulthood With Mevalonate Kinase Deficiency |
| Q48277726 | One novel and two uncommon MEFV mutations in Japanese patients with familial Mediterranean fever: a clinicogenetic study |
| Q36762550 | Oscillations in the immune system |
| Q35188632 | PFAPA syndrome: with regard to a case |
| Q46705719 | PReS-FINAL-2330: Canakinumab treatment in patients with HIDS. |
| Q40530190 | Periodic fever, mild arthralgias, and reversible moderate and severe organ inflammation associated with the V198M mutation in the CIAS1 gene in three German patients--expanding phenotype of CIAS1 related autoinflammatory syndrome |
| Q40556454 | Periodic fevers: from genetics to clinical medicine |
| Q38954801 | Periodontal and other oral manifestations of immunodeficiency diseases |
| Q38866091 | Phenotype-genotype updates from familial Mediterranean fever database registry of Mansoura University Children' Hospital, Mansoura, Egypt |
| Q40256653 | Phytochemical studies and cytotoxicity evaluations of Colchicum tunicatum Feinbr and Colchicum hierosolymitanum Feinbr (Colchicaceae): two native Jordanian meadow saffrons. |
| Q40527582 | Recurrent bouts of fever accompanied by abdominal pain and emesis |
| Q37468460 | Recurrent febrile syndromes: what a rheumatologist needs to know |
| Q37407556 | Recurrent fever and rash. |
| Q36228479 | Regulation of phosphatidylinositol 3-kinase by polyisoprenyl phosphates in neutrophil-mediated tissue injury. |
| Q33773150 | Relationship between serum interleukin-1beta levels and acute phase response proteins in patients with familial Mediterranean fever |
| Q37187378 | S100A12 is a novel molecular marker differentiating systemic-onset juvenile idiopathic arthritis from other causes of fever of unknown origin |
| Q40436133 | Schnitzler's syndrome with urticaria vasculitis |
| Q34559225 | Serum amyloid A serum concentrations and genotype do not explain low incidence of amyloidosis in Hyper-IgD syndrome. |
| Q57420160 | Serum amyloid A: production by human white adipocyte and regulation by obesity and nutrition |
| Q40199201 | Serum galectin-3 levels were associated with proteinuria in patients with Familial Mediterranean Fever |
| Q38116809 | Sterol metabolism disorders and neurodevelopment-an update. |
| Q40556439 | TNF receptor-associated periodic syndrome (TRAPS): clinical aspects and physiopathology of a rare familial disease |
| Q40562330 | Targeted disruption of pyrin, the FMF protein, causes heightened sensitivity to endotoxin and a defect in macrophage apoptosis |
| Q40512944 | Tendonitis in variant hyperimmunoglobulinaemia D and periodic fever syndrome--a rare disease with a new symptom |
| Q53621350 | The CYP4502D6 *4 and *6 alleles are the molecular genetic markers for drug response: implications in colchicine non-responder FMF patients. |
| Q28383855 | The PYRIN domain in signal transduction |
| Q28070297 | The challenge of autoinflammatory syndromes: with an emphasis on hyper-IgD syndrome |
| Q24312686 | The estrogen-responsive B box protein: a novel enhancer of interleukin-1beta secretion |
| Q40267982 | The scintigraphic evaluation and genetic correlation of joint involvements in pediatric patients with familial Mediterranean fever |
| Q37208960 | The spectrum of monogenic autoinflammatory syndromes: understanding disease mechanisms and use of targeted therapies |
| Q35640323 | The systemic amyloidoses: clearer understanding of the molecular mechanisms offers hope for more effective therapies |
| Q40316862 | Trace element levels in patients with familial mediterranean Fever |
| Q40544623 | Tumor necrosis factor receptor superfamily 1A-associated periodic syndrome (TRAPS) |
| Q40552828 | Tumor necrosis factor receptor-associated periodic syndrome characterized by a mutation affecting the cleavage site of the receptor: implications for pathogenesis |
| Q40510589 | Tumour necrosis factor receptor-associated periodic syndrome. A rare differential diagnosis of multiple sclerosis |
| Q40551844 | Two German CINCA (NOMID) patients with different clinical severity and response to anti-inflammatory treatment |
| Q40459571 | Urticaria as a cutaneous sign of adult-onset Still's disease. |
| Q83811771 | [Autoinflammatory syndromes] |
| Q54770315 | [Hot and cold in periodic fever]. |
| Q40376766 | [Molecular diagnostics of hereditary fever syndromes. Familial Mediterranean fever (FMF), hyperimmunoglobulin D syndrome (HIDS), tumor necrosis factor receptor-associated periodic syndrome (TRAPS), cryopyrin-associated periodic syndrome (CAPS: FCAS, |
| Q40466032 | [Periodic fever syndromes]. |
| Q42375820 | Approche à la fièvre récurrente de l’enfant |