Browsing by Author Potter, BK

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Issue DateTitleAuthor(s)
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
2016The health system impact of false positive newborn screening results for medium-chain acyl-CoA dehydrogenase deficiency: A cohort studyKaraceper, MD; Chakraborty, P; Coyle, D; Wilson, K; Kronick, JB; Hawken, S; Davies, C; Brownell, M; Dodds, L; Feigenbaum, A; Fell, DB; Grosse, SD; Guttmann, A; Laberge, A-M; Mhanni, A; Miller, FA; Mitchell, JJ; Nakhla, M; Prasad, C; Rockman-Greenberg, C; Sparkes, R; Wilson, BJ; 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
2018Using a meta-narrative literature review and focus groups with key stakeholders to identify perceived challenges and solutions for generating robust evidence on the effectiveness of treatments for rare diseasesTingley, K; Coyle, D; Graham, ID; Sikora, L; Chakraborty, P; Wilson, K; Mitchell, JJ; Stockler-Ipsiroglu, S; Potter, BK