| review article | Q7318358 |
| scholarly article | Q13442814 |
| P2093 | author name string | Raphaela Goldbach-Mansky | |
| John G Ryan | |||
| P2860 | cites work | A proposed classification of the immunological diseases | Q21144701 |
| A pilot study of IL-1 inhibition by anakinra in acute gout | Q21195421 | ||
| 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 | Q24337040 | ||
| AA amyloidosis complicating hyperimmunoglobulinemia D with periodic fever syndrome: a report of two cases | Q24338312 | ||
| Structural and functional insights into the B30.2/SPRY domain. | Q24541987 | ||
| Pyrin binds the PSTPIP1/CD2BP1 protein, defining familial Mediterranean fever and PAPA syndrome as disorders in the same pathway | Q24655872 | ||
| Autoinflammatory gene mutations in Behçet's disease | Q24674998 | ||
| Beneficial response to anakinra and thalidomide in Schnitzler's syndrome | Q24675386 | ||
| Structural basis for PRYSPRY-mediated tripartite motif (TRIM) protein function | Q24684586 | ||
| A human homologue of the Drosophila Toll protein signals activation of adaptive immunity | Q28131769 | ||
| Gout-associated uric acid crystals activate the NALP3 inflammasome | Q28131797 | ||
| Interferon-alpha/beta-mediated innate immune mechanisms in dermatomyositis | Q28246912 | ||
| Approach to genetic analysis in the diagnosis of hereditary autoinflammatory syndromes | Q28277791 | ||
| Cryopyrin activates the inflammasome in response to toxins and ATP | Q28291313 | ||
| The family of five: TIR-domain-containing adaptors in Toll-like receptor signalling | Q29615457 | ||
| Bacterial RNA and small antiviral compounds activate caspase-1 through cryopyrin/Nalp3 | Q29615598 | ||
| The expanding spectrum of systemic autoinflammatory disorders and their rheumatic manifestations | Q30757410 | ||
| CARD15 single nucleotide polymorphisms 8, 12 and 13 are not increased in ethnic Danes with sarcoidosis | Q47659047 | ||
| Clinical and genetic characterization of Italian patients affected by CINCA syndrome. | Q51913494 | ||
| Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromes. | Q54806502 | ||
| Structural, functional and immunologic characterization of folded subdomains in the Ro52 protein targeted in Sjögren's syndrome | Q60548207 | ||
| Antimalarial agents: closing the gate on Toll-like receptors? | Q79158393 | ||
| Pediatric granulomatous arthritis: an international registry | Q79158593 | ||
| A role for geranylgeranylation in interleukin-1beta secretion | Q79318151 | ||
| Diagnostics and therapeutic insights in a severe case of mevalonate kinase deficiency | Q79685433 | ||
| Classification of non-bacterial osteitis: retrospective study of clinical, immunological and genetic aspects in 89 patients | Q79748605 | ||
| Response to IL-1-receptor antagonist in a child with familial cold autoinflammatory syndrome | Q79774748 | ||
| Interstitial pneumonitis in Blau syndrome with documented mutation in CARD15 | Q80060015 | ||
| Treatment of patients with neonatal-onset multisystem inflammatory disease/chronic infantile neurologic, cutaneous, articular syndrome: comment on the article by Matsubara et al | Q80388352 | ||
| Behçet's disease and other autoinflammatory conditions: what's in a name? | Q81450913 | ||
| Intrafamilial variable phenotypic expression of a CIAS1 mutation: from Muckle-Wells to chronic infantile neurological cutaneous and articular syndrome | Q81597330 | ||
| Identification of small heat shock protein B8 (HSP22) as a novel TLR4 ligand and potential involvement in the pathogenesis of rheumatoid arthritis | Q83367358 | ||
| The inflammasome: first line of the immune response to cell stress | Q33998873 | ||
| Neonatal-onset multisystem inflammatory disease responsive to interleukin-1beta inhibition | Q34262569 | ||
| A severe case of chronic infantile neurologic, cutaneous, articular syndrome treated with biologic agents | Q34542129 | ||
| Gout: new insights into an old disease. | Q34569614 | ||
| Toll-like receptors in systemic autoimmune disease | Q34576448 | ||
| Innate recognition of intracellular bacteria. | Q34584530 | ||
| Natural history and outcome in systemic AA amyloidosis | Q34635240 | ||
| The B30.2 domain of pyrin, the familial Mediterranean fever protein, interacts directly with caspase-1 to modulate IL-1beta production | Q34684433 | ||
| MyD88-dependent IL-1 receptor signaling is essential for gouty inflammation stimulated by monosodium urate crystals | Q34872946 | ||
| A promoter haplotype of the interleukin-18 gene is associated with juvenile idiopathic arthritis in the Japanese population | Q34897164 | ||
| The clinical continuum of cryopyrinopathies: novel CIAS1 mutations in North American patients and a new cryopyrin model | Q35064730 | ||
| Monocytes from familial cold autoinflammatory syndrome patients are activated by mild hypothermia | Q35064754 | ||
| "Periodic fever" without fever: two cases of non-febrile TRAPS with mutations in the TNFRSF1A gene presenting with episodes of inflammation or monosymptomatic amyloidosis | Q35637417 | ||
| Clinical significance of P46L and R92Q substitutions in the tumour necrosis factor superfamily 1A gene | Q35637824 | ||
| Intrafamilial segregation analysis of the p.E148Q MEFV allele in familial Mediterranean fever | Q35637910 | ||
| A decision tree for genetic diagnosis of hereditary periodic fever in unselected patients | Q35638094 | ||
| Abnormal disulfide-linked oligomerization results in ER retention and altered signaling by TNFR1 mutants in TNFR1-associated periodic fever syndrome (TRAPS) | Q35849941 | ||
| CATERPILLERs, pyrin and hereditary immunological disorders | Q36405072 | ||
| Intracellular pattern recognition receptors in the host response | Q36528528 | ||
| Recent advances in crystal-induced acute inflammation | Q36728481 | ||
| TLR-dependent and TLR-independent pathways of type I interferon induction in systemic autoimmunity | Q36811126 | ||
| A missense mutation in pstpip2 is associated with the murine autoinflammatory disorder chronic multifocal osteomyelitis | Q37053052 | ||
| Favourable effect of TNF-alpha inhibitor (infliximab) on Blau syndrome in monozygotic twins with a de novo CARD15 mutation | Q39341447 | ||
| The SPRY domain of Pyrin, mutated in familial Mediterranean fever patients, interacts with inflammasome components and inhibits proIL-1beta processing | Q40146198 | ||
| Disease-associated mutations in CIAS1 induce cathepsin B-dependent rapid cell death of human THP-1 monocytic cells | Q40197311 | ||
| TLR7 ligands induce higher IFN-alpha production in females. | Q40247926 | ||
| The SPRY domain of SSB-2 adopts a novel fold that presents conserved Par-4-binding residues | Q40337569 | ||
| Cryopyrin and pyrin activate caspase-1, but not NF-kappaB, via ASC oligomerization. | Q40394627 | ||
| Pyrin levels in human monocytes and monocyte-derived macrophages regulate IL-1beta processing and release | Q40445201 | ||
| Allogeneic bone marrow transplantation in mevalonic aciduria | Q40446064 | ||
| Eprodisate for the treatment of renal disease in AA amyloidosis. | Q40447968 | ||
| Association between celiac sprue and cryopyrin associated autoinflammatory disorders: a case report. | Q40448119 | ||
| Country as the primary risk factor for renal amyloidosis in familial Mediterranean fever. | Q40451318 | ||
| First report of macrophage activation syndrome in hyperimmunoglobulinemia D with periodic fever syndrome. | Q40458834 | ||
| A cryopyrin-associated periodic syndrome with joint destruction. | Q40461894 | ||
| Defective apoptosis of peripheral-blood lymphocytes in hyper-IgD and periodic fever syndrome. | Q40463375 | ||
| Arthropathy of neonatal onset multisystem inflammatory disease (NOMID/CINCA). | Q40463468 | ||
| Hereditary periodic fever with systemic amyloidosis: is hyper-IgD syndrome really a benign disease? | Q40471559 | ||
| Inflammatory/demyelinating central nervous system involvement in familial Mediterranean fever (FMF): coincidence or association? | Q40484897 | ||
| Structure of the PRYSPRY-domain: implications for autoinflammatory diseases | Q40490657 | ||
| Somatic mosaicism of CIAS1 in a patient with chronic infantile neurologic, cutaneous, articular syndrome. | Q40495195 | ||
| Rapid responses to anakinra in patients with refractory adult-onset Still's disease | Q40507008 | ||
| Clinical and genetic heterogeneity among Spanish patients with recurrent autoinflammatory syndromes associated with the CIAS1/PYPAF1/NALP3 gene. | Q40519235 | ||
| Criteria for the diagnosis of familial Mediterranean fever | Q40645936 | ||
| Synovitis in familial Mediterranean fever | Q40814339 | ||
| Infantile multisystem inflammatory disease: a specific syndrome? | Q40819603 | ||
| Hyperimmunoglobulinaemia D syndrome in India: report of two siblings with a novel mutation | Q42955219 | ||
| Neutrophils from patients with TNFRSF1A mutations display resistance to tumor necrosis factor-induced apoptosis: pathogenetic and clinical implications | Q46969655 | ||
| Increased interleukin-18 expression in bone marrow of a patient with systemic juvenile idiopathic arthritis and unrecognized macrophage-activation syndrome | Q47368371 | ||
| P433 | issue | 1 | |
| P304 | page(s) | 66-75 | |
| P577 | publication date | 2008-01-01 | |
| P1433 | published in | Current Opinion in Rheumatology | Q15750473 |
| P1476 | title | The spectrum of autoinflammatory diseases: recent bench to bedside observations | |
| P478 | volume | 20 |
| Q27007734 | A clear and present danger: inflammasomes DAMPing down disorders of pregnancy |
| Q37966720 | A retrospective review of autoinflammatory diseases in Saudi children at a rheumatology clinic. |
| Q57154732 | An update on the genetic causes of hyperuricemia and gout |
| Q36753558 | Autoinflammatory gene polymorphisms and susceptibility to UK juvenile idiopathic arthritis |
| Q37279367 | Behçet's disease: recent advances in early diagnosis and effective treatment |
| Q35029382 | Chronic Proliferative Dermatitis in Mice: NFκB Activation Autoinflammatory Disease |
| Q30465378 | Cryopyrin-associated periodic syndromes: otolaryngologic and audiologic manifestations |
| Q37077793 | From the Mediterranean to the sea of Japan: the transcontinental odyssey of autoinflammatory diseases |
| Q47649630 | M-CSF induces the expression of a membrane-bound form of IL-18 in a subset of human monocytes differentiating in vitro toward macrophages |
| Q37733733 | Monogenic Autoinflammatory Diseases with Mendelian Inheritance: Genes, Mutations, and Genotype/Phenotype Correlations. |
| Q37845749 | Monogenic autoinflammatory syndromes at a dermatological level |
| Q36159273 | Multiplicative interaction of functional inflammasome genetic variants in determining the risk of gout |
| Q37395365 | Rare monogenetic syndromes in rheumatology practice |
| Q37834022 | Setting up TRAPS. |
| Q37800522 | The inflammasome regulatory pathway and infections: Role in pathophysiology and clinical implications |
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