Browsing by Author Canadian Inherited Metabolic Diseases Research Network

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
or enter first few letters:  
Showing results 1 to 2 of 2
Issue DateTitleAuthor(s)
2017Establishing 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
2015Scoping review of patient- and family-oriented outcomes and measures for chronic pediatric disease.Karaceper, MD; Trakadis, Y; Mitchell, JJ; Chakraborty, P; Tingley, K; Coyle, D; Grosse, SD; Kronick, JB; Laberge, A-M; Little, J; Prasad, C; Sikora, L; Siriwardena, K; Sparkes, R; Speechley, KN; Stockler, S; Wilson, BJ; Wilson, K; Zayed, R; Potter, BK; Canadian Inherited Metabolic Diseases Research Network