Cardiac involvement in adult-onset Still's disease: Manifestations, treatments and outcomes in a retrospective study of 28 patients

Reproducibility and diagnostic value of a new method using ratios to diagnose anterior atlanto-axial subluxation on plain radiographs

Spectrum and Prognosis of Antineutrophil Cytoplasmic Antibody-associated Vasculitis-related Bronchiectasis: Data from 61 Patients

Therapeutic innovation in adult-onset Still's disease (and other rare inflammatory disorders): how to secure evidence-based medicine?

Fibrosis Development in HOCl-Induced Systemic Sclerosis: A Multistage Process Hampered by Mesenchymal Stem Cells

Intriguing Relationships Between Cancer and Systemic Sclerosis: Role of the Immune System and Other Contributors

About the complexity of adult onset Still's disease… and advances still required for its management

[A small spleen]

The clinical spectrum and therapeutic management of hypocomplementemic urticarial vasculitis: data from a French nationwide study of fifty-seven patients

Inflammatory bowel diseases in anti-neutrophil cytoplasmic antibody-associated vasculitides: 11 retrospective cases from the French Vasculitis Study Group

Central nervous system involvement of granulomatosis with polyangiitis: clinical-radiological presentation distinguishes different outcomes

Adult onset Still's disease (AOSD) in the era of biologic therapies: dichotomous view for cytokine and clinical expressions

[Evolution and prognosis of adult onset Still's disease. A monocentric study of 17 patients]

[Headache due to temporal arteritis]

[Headache as an indicator of systemic disease]

Distribution of HLA-DRB1 alleles of patients with polymyalgia rheumatica and giant cell arteritis in a Mediterranean population

[Paraneoplastic seropositive polyarthritis]

Prevalence of anti-neutrophil cytoplasmic antibody-associated vasculitis in the south of France, using the capture-recapture method

Prevalence and predictors of atlanto-axial subluxation in rheumatoid arthritis after 12-years' follow-up (ESPOIR Cohort)

Localized versus systemic granulomatosis with polyangiitis: data from the French Vasculitis Study Group Registry

Microscopic polyangiitis: Clinical characteristics and long-term outcomes of 378 patients from the French Vasculitis Study Group Registry

Mortality in systemic necrotizing vasculitides: A retrospective analysis of the French Vasculitis Study Group registry

Brief Report: Childhood-Onset Systemic Necrotizing Vasculitides: Long-Term Data From the French Vasculitis Study Group Registry

Comparative study of granulomatosis with polyangiitis subsets according to ANCA status: data from the French Vasculitis Study Group Registry

Childhood- versus adult-onset ANCA-associated vasculitides: A nested, matched case-control study from the French Vasculitis Study Group Registry

Impact of MPO-ANCA-mediated oxidative imbalance on renal vasculitis

Eosinophilic granulomatosis with polyangiitis (Churg-Strauss): clinical characteristics and long-term followup of the 383 patients enrolled in the French Vasculitis Study Group cohort

[Incidence and presentation of the central neurological manifestations of Wegener's granulomatosis: a monocentric study of 14 cases]

Chronological interplay, clinical features, and treatments among patients with cancer and primary Sjögren's syndrome

The interplay between cognition, depression, anxiety, and sleep in primary Sjogren's syndrome patients

Mastitis associated with Sjögren's syndrome: a series of nine cases

A multicentre study of 95 biopsy-proven cases of renal disease in primary Sjögren's syndrome

[Prevention of infections in adults and adolescents with systemic lupus erythematosus: Guidelines for the clinical practice based on the literature and expert opinion]

[Screening and management of cardiovascular risk factors in systemic lupus erythematosus: Recommendations for clinical practice based on the literature and expert opinion]

Localized Cutaneous Leishmaniasis due to Leishmania infantum in a Patient Treated with Infliximab

Rituximab: Recommendations of the French Vasculitis Study Group (FVSG) for induction and maintenance treatments of adult, antineutrophil cytoplasm antibody-associated necrotizing vasculitides

Autoinflammatory gene mutations in Behçet's disease

Comment on the article entitled "Antineutrophil cytoplasmic antibody-associated vasculitides and IgG4-related disease: A new overlap syndrome" (Autoimmunity Reviews 16 (2017) 1036-1043)

Joint involvement in Noonan syndrome. A retrospective paediatric descriptive study

Biphasic Temporal Relationship between Cancers and Systemic Sclerosis: A Clinical Series from Montpellier University Hospital and Review of the Literature

[Screening and management of cardiovascular risk factors in systemic lupus erythematosus: Recommendations for clinical practice based on the literature and expert opinion]

Acute and regressive scleroderma concomitant to an acute CMV primary infection

Autoinflammatory gene mutations in Behçet's disease