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- Journal Article
- A1
- open access
Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy
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- Journal Article
- A1
- open access
Seven-year follow-up of infliximab therapy in rheumatoid arthritis patients with severe long-standing refractory disease : attrition rate and evolution of disease activity
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- Journal Article
- A1
- open access
The Belgian MIRA (MabThera In Rheumatoid Arthritis) registry: clues for the optimization of rituximab treatment strategies
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Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus
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The majority of the genetic risk for Paget's disease of bone is explained by genetic variants close to the CSF1, OPTN, TM7SF4, and TNFRSF11A genes
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Genetic variation in the TNFRSF11A gene encoding RANK is associated with susceptibility to Paget's disease of bone
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Validation of a manual ability questionnaire in patients with systemic sclerosis
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Founder effect in different European countries for the recurrent P392L SQSTM1 mutation in Paget's disease of bone