Dutch juvenile idiopathic arthritis patients, carers and clinicians create a research agenda together following the James Lind Alliance method: a study protocol

• Egile Nagusiak: Casper G. Schoemaker (Egilea), Wineke Armbrust (Egilea), Joost F. Swart (Egilea), Sebastiaan J. Vastert (Egilea), Jorg van Loosdregt (Egilea), Anouk Verwoerd (Egilea), Caroline Whiting (Egilea), Katherine Cowan (Egilea), Wendy Olsder (Egilea), Els Versluis (Egilea), Rens van Vliet (Egilea), Marlous J. Fernhout (Egilea), Sanne L. Bookelman (Egilea), Jeannette Cappon (Egilea), J. Merlijn van den Berg (Egilea), Ellen Schatorjé (Egilea), Petra C. E. Hissink Muller (Egilea), Sylvia Kamphuis (Egilea), Joke de Boer (Egilea), Otto T. H. M. Lelieveld (Egilea), Janjaap van der Net (Egilea), Karin R. Jongsma (Egilea), Annemiek van Rensen (Egilea), Christine Dedding (Egilea), Nico M. Wulffraat (Egilea)
• Formatua: Liburua
• Argitaratua: BMC, 2018-09-01T00:00:00Z.
• Gaiak: article
• Sarrera elektronikoa: Connect to this object online.

Abstract Background Research on Juvenile Idiopathic Arthritis (JIA) should support patients, caregivers/parents (carers) and clinicians to make important decisions in the consulting room and eventually to improve the lives of patients with JIA. Thus far these end-users of JIA-research have rarely be...