Adding patient-reported outcomes to a multisite registry to quantify quality of life and experiences of disease and treatment for youth with juvenile idiopathic arthritis
Crossref DOI link:
Update policy: https://doi.org/10.1007/SPRINGER_CROSSMARK_POLICY
Weitzman, Elissa R.
Wisk, Lauren E.
Salimian, Parissa K.
Magane, Kara M.
Hersh, Aimee O.
Mandl, Kenneth D.
Funding for this research was provided by:
U.S. National Library of Medicine (R01LM011185)
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