Browsing by Author Stockler, S

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Showing results 1 to 5 of 5
Issue DateTitleAuthor(s)
2016Child and family experiences with inborn errors of metabolism: a qualitative interview study with representatives of patient groupsTingley, K; Chakraborty, P; Coyle, D; Kronick, JB; Laberge, A-M; Little, J; Miller, FA; Mitchell, JJ; Prasad, C; Siddiq, S; Siriwardena, K; Sparkes, R; Speechley, KN; Stockler, S; Trakadis, Y; Wilson, BJ; Wilson, K; Potter, BK
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
2016Experiences of caregivers of children with inherited metabolic diseases: A qualitative studySiddiq, S; Wilson, BJ; Graham, ID; Lamoureux, M; Khangura, SD; Tingley, K; Tessier, L; Chakraborty, P; Coyle, D; Dyack, S; Gillis, J; Greenberg, C; Hayeems, RZ; Jain-Ghai, S; Kronick, JB; Laberge, A-M; Little, J; Mitchell, JJ; Prasad, C; Siriwardena, K; Sparkes, R; Speechley, KN; Stockler, S; Trakadis, Y; Wafa, S; Walia, J; Wilson, K; Yuskiv, N; Potter, BK
22-Mar-2019Health services use among children diagnosed with medium-chain acyl-CoA dehydrogenase deficiency through newborn screening: A cohort study in Ontario, CanadaKaraceper, MD; Khangura, SD; Wilson, K; Coyle, D; Brownell, M; Davies, C; Dodds, L; Feigenbaum, A; Fell, DB; Grosse, SD; Guttmann, A; Hawken, S; Hayeems, RZ; Kronick, JB; Laberge, AM; Little, J; Mhanni, A; Mitchell, JJ; Nakhla, M; Potter, M; Prasad, C; Rockman-Greenberg, C; Sparkes, R; Stockler, S; Ueda, K; Vallance, H; Wilson, BJ; Chakraborty, P; Potter, BK
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