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Genes and Immunity|May 4, 2012
Evidence that deletion at FCGR3B is a risk factor for systemic sclerosisC McKinney, J C A Broen, M C Vonk, et al.
Annals of the Rheumatic Diseases|July 26, 2011
Clinical prediction of 5-year survival in systemic sclerosis: validation of a simple prognostic model in EUSTAR centresJ Fransen, D Popa-Diaconu, R Hesselstrand, et al.
Annals of the Rheumatic Diseases|December 15, 2010
NLRP1 influences the systemic sclerosis phenotype: a new clue for the contribution of innate immunity in systemic sclerosis-related fibrosing alveolitis pathogenesisP Dieudé, M Guedj, J Wipff, et al.
European Journal of Internal Medicine|April 10, 2024
Clinical significance of the anti-Nucleolar Organizer Region 90 antibodies (NOR90) in systemic sclerosis: Analysis of the European Scleroderma Trials and Research (EUSTAR) cohort and a systematic literature reviewA Dima, M C Vonk, A Garaiman, et al.
Arthritis and Rheumatism|December 17, 2010
Association of the CD226 Ser(307) variant with systemic sclerosis: evidence of a contribution of costimulation pathways in systemic sclerosis pathogenesisP Dieudé, M Guedj, M E Truchetet, et al.
Arthritis and Rheumatism|June 18, 2010
Association of a KCNA5 gene polymorphism with systemic sclerosis-associated pulmonary arterial hypertension in the European Caucasian populationJ Wipff, P Dieudé, M Guedj, et al.
Annals of the Rheumatic Diseases|March 13, 2009
Prevalence and factors associated with left ventricular dysfunction in the EULAR Scleroderma Trial and Research group (EUSTAR) database of patients with systemic sclerosisY Allanore, C Meune, M C Vonk, et al.
Human Molecular Genetics|March 17, 2009
The STAT4 gene influences the genetic predisposition to systemic sclerosis phenotypeB Rueda, J Broen, C Simeon, et al.
Annals of the Rheumatic Diseases|October 10, 2009
BANK1 functional variants are associated with susceptibility to diffuse systemic sclerosis in CaucasiansB Rueda, P Gourh, J Broen, et al.
Annals of the Rheumatic Diseases|December 7, 2010
Analysis of the influence of PTPN22 gene polymorphisms in systemic sclerosisL M Diaz-Gallo, P Gourh, J Broen, et al.
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