How to routinely collect data on patient-reported outcome and experience measures in renal registries in Europe: an expert consensus meeting.
Breckenridge K, Abbott D, Bekker H, Briançon S, Cullen R, Garneata L, Gibbons E, Jager KJ, Lønning K, Metcalfe W, Morton RL, Murtagh FM, Prutz K, Robertson S, Rychlik I, Sharp L, Schon S, Speyer E, Tentori F, van der Veer SN, Caskey FJ
DOI: 10.1093/ndt/gfv209