Diagnostic and management of life-threatening Adult-Onset Still Disease: a French nationwide multicenter study and systematic literature review.

scientific article

Diagnostic and management of life-threatening Adult-Onset Still Disease: a French nationwide multicenter study and systematic literature review. is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1186/S13054-018-2012-2
P932PMC publication ID5896069
P698PubMed publication ID29642928

P50authorAntoine NéelQ61651271
Anaïs WahbiQ88333297
Cécile GoujardQ88521925
P2093author name stringCédric Bretonnière
Dorothée Carpentier
Guillaume Geri
Olivier Decaux
Hervé Maisonneuve
Mohamed Hamidou
Jacques Pouchot
Laurence Fardet
Pascal Godmer
Benoit Tessoulin
Arnaud Mari
Julien Boileau
Jean-Marc Ziza
P2860cites workLymph node IL-18 expression in adult-onset Still's disease.Q51824485
The Logistic Organ Dysfunction system. A new way to assess organ dysfunction in the intensive care unit. ICU Scoring Group.Q52199824
Corticosteroid sparing effect of low dose methotrexate treatment in adult Still's disease.Q54105583
Interleukin-18 as a novel diagnostic marker and indicator of disease severity in adult-onset Still's diseaseQ74242469
Proposal for a new set of classification criteria for adult-onset still diseaseQ78069999
Clinical manifestations but not cytokine profiles differentiate adult-onset Still's disease and sepsisQ84973391
Adult-onset Still's diseaseQ26852631
Development and validation of the HScore, a score for the diagnosis of reactive hemophagocytic syndromeQ28239135
APACHE II: a severity of disease classification systemQ29547729
A new Simplified Acute Physiology Score (SAPS II) based on a European/North American multicenter studyQ29615430
Reactive haemophagocytic syndrome in adult-onset Still's disease: a report of six patients and a review of the literatureQ33370577
Life-threatening complications of adult-onset Still's diseaseQ33412732
Adult-onset still disease: manifestations, treatment, outcome, and prognostic factors in 57 patientsQ33414045
Reactive hemophagocytic syndrome in adult-onset Still disease: clinical features, predictive factors, and prognosis in 21 patientsQ33420069
Epidemiology of adult Still's disease: estimate of the incidence by a retrospective study in west FranceQ33578168
Preliminary criteria for classification of adult Still's diseaseQ34405573
Synovial tissue interleukin-18 expression and the response to treatment in patients with inflammatory arthritisQ35553556
Tumour necrosis factor alpha blocking agents in refractory adult Still's disease: an observational study of 20 casesQ35555229
Efficacy and long-term follow-up of IL-1R inhibitor anakinra in adults with Still's disease: a case-series studyQ35557906
Severe imbalance of IL-18/IL-18BP in patients with secondary hemophagocytic syndromeQ35847631
Myocarditis in adult-onset still diseaseQ36150742
Efficacy of Anakinra in Refractory Adult-Onset Still's Disease: Multicenter Study of 41 Patients and Literature Review.Q36195807
Understanding organ dysfunction in hemophagocytic lymphohistiocytosisQ37144156
Interleukin-1 Receptor Blockade Is Associated With Reduced Mortality in Sepsis Patients With Features of Macrophage Activation Syndrome: Reanalysis of a Prior Phase III TrialQ37735696
Biological treatment in adult-onset Still's diseaseQ38049762
Application of the 2016 EULAR/ACR/PRINTO Classification Criteria for Macrophage Activation Syndrome in Patients with Adult-onset Still Disease.Q40060914
Efficacy of tocilizumab in conventional treatment-refractory adult-onset Still's disease: multicenter retrospective open-label study of thirty-four patients.Q40218234
Tocilizumab in refractory adult Still's diseaseQ40350291
Reactive hemophagocytic syndrome in adult-onset Still disease: clinical features and long-term outcome: a case-control study of 8 patientsQ40368756
Adult-onset Still disease with hemophagocytic syndrome treated with cyclosporineQ40492169
Rapid responses to anakinra in patients with refractory adult-onset Still's diseaseQ40507008
Etanercept in the treatment of adult patients with Still's diseaseQ40578875
May anakinra be used earlier in adult onset Still disease?Q43080826
Infliximab in the treatment of adult Still's disease refractory to conventional therapyQ43640728
Confirmatory interleukin-1 receptor antagonist trial in severe sepsis: a phase III, randomized, double-blind, placebo-controlled, multicenter trial. The Interleukin-1 Receptor Antagonist Sepsis Investigator GroupQ44267568
Efficacy of traditional and biologic agents in different clinical phenotypes of adult-onset Still's diseaseQ44554787
P275copyright licenseCreative Commons Attribution 4.0 InternationalQ20007257
P6216copyright statuscopyrightedQ50423863
P433issue1
P304page(s)88
P577publication date2018-04-11
P1433published inCritical CareQ5186602
P1476titleDiagnostic and management of life-threatening Adult-Onset Still Disease: a French nationwide multicenter study and systematic literature review
P478volume22

Reverse relations

cites work (P2860)
Q90177179Adult-onset Still's disease revealed by a complete atrioventricular block, totally regressive under corticosteroid therapy
Q90464748Anakinra in Still's disease: a profile of its use
Q91910547Management of adult-onset Still's disease with interleukin-1 inhibitors: evidence- and consensus-based statements by a panel of Italian experts
Q64235820Managing Adult-onset Still's disease: The effectiveness of high-dosage of corticosteroids as first-line treatment in inducing the clinical remission. Results from an observational study
Q57143910Mechanisms, biomarkers and targets for adult-onset Still's disease
Q101237305Title: Cytokine release syndrome is not usually caused by secondary hemophagocytic lymphohistiocytosis in a cohort of 19 critically ill COVID-19 patients

Search more.