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Issue Date | Title | Author(s) |
---|---|---|
2017 | Establishing core outcome sets for phenylketonuria (PKU) and medium-chain Acyl-CoA dehydrogenase (MCAD) deficiency in children: study protocol for systematic reviews and Delphi surveys. | Potter, BK; Hutton, B; Clifford, TJ; Pallone, N; Smith, M; Stockler, S; Chakraborty, P; Barbeau, P; Garritty, CM; Pugliese, M; Rahman, A; Skidmore, B; Tessier, L; Tingley, K; Coyle, D; Greenberg, CR; Korngut, L; MacKenzie, A; Mitchell, JJ; Nicholls, S; Offringa, M; Schulze, A; Taljaard, M; Canadian Inherited Metabolic Diseases Research Network |