The IN-DEEP project “INtegrating and Deriving Evidence, Experiences, Preferences”: a web information model on magnetic resonance imaging for people with multiple sclerosis

[1] Köpke S(2018)Information provision for people with multiple sclerosis Cochrane Database Syst Rev. 10 CD008757-650

[2] Solari A(2004)Decisional role preferences, risk knowledge and information interests in patients with multiple sclerosis Mult Scler 10 643-91

[3] Rahn A(2008)Participation in medical decisionmaking: attitudes of Italians with multiple sclerosis J Neurol Sci 275 86-312

[4] Khan F(2017)Shared decision making and autonomy among US participants with multiple sclerosis in the NARCOMS Registry Int J MS Care 19 303-328

[5] Heesen C(2013)Preferred sources of health information in persons with multiple sclerosis: degree of trust and information sought J Med Internet Res 15 e67-190

[6] Giordano A(2010)What constitutes evidence-based patient information? Overview of discussed criteria Patient Educ Couns 78 316-577

[7] Heesen C(2015)A summary to communicate evidence from systematic reviews to the public improved understanding and accessibility of information: a randomized controlled trial J Clin Epidemiol 68 182-96

[8] Kasper J(2010)Presenting the results of cochrane systematic reviews to a consumer audience: a qualitative study Med Decis Mak 30 566-23

[9] Segal J(2011)Communicating data about the benefits and harms of treatment: a randomized trial Ann Intern Med 155 87-119

[10] Kopke S(2011)Using alternative statistical formats for presenting risks and risk reductions Cochrane Database Syst Rev 12 13-737

[1] Köpke S(2018)Information provision for people with multiple sclerosis Cochrane Database Syst Rev. 10 CD008757-650

[2] Solari A(2004)Decisional role preferences, risk knowledge and information interests in patients with multiple sclerosis Mult Scler 10 643-91

[3] Rahn A(2008)Participation in medical decisionmaking: attitudes of Italians with multiple sclerosis J Neurol Sci 275 86-312

[4] Khan F(2017)Shared decision making and autonomy among US participants with multiple sclerosis in the NARCOMS Registry Int J MS Care 19 303-328

[5] Heesen C(2013)Preferred sources of health information in persons with multiple sclerosis: degree of trust and information sought J Med Internet Res 15 e67-190

[6] Giordano A(2010)What constitutes evidence-based patient information? Overview of discussed criteria Patient Educ Couns 78 316-577

[7] Heesen C(2015)A summary to communicate evidence from systematic reviews to the public improved understanding and accessibility of information: a randomized controlled trial J Clin Epidemiol 68 182-96

[8] Kasper J(2010)Presenting the results of cochrane systematic reviews to a consumer audience: a qualitative study Med Decis Mak 30 566-23

[9] Segal J(2011)Communicating data about the benefits and harms of treatment: a randomized trial Ann Intern Med 155 87-119

[10] Kopke S(2011)Using alternative statistical formats for presenting risks and risk reductions Cochrane Database Syst Rev 12 13-737