Health services use by children identified as heterozygous hemoglobinopathy mutation carriers via newborn screening von Khangura, Sara D., Potter, Beth K., Davies, Christine, Ducharme, Robin, Bota, A. Brianne, Hawken, Steven, Wilson, Kumanan, Karaceper, Maria D., Klaassen, Robert J., Little, Julian, Simpson, Ewurabena, Chakraborty, Pranesh

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Health services use among children diagnosed with medium-chain acyl-CoA dehydrogenase deficiency through newborn screening: a cohort study in Ontario, Canada von Karaceper, Maria D, Khangura, Sara D, Wilson, Kumanan, Coyle, Doug, Brownell, Marni, Davies, Christine, Dodds, Linda, Feigenbaum, Annette, Fell, Deshayne B, Grosse, Scott D, Guttmann, Astrid, Hawken, Steven, Hayeems, Robin Z, Kronick, Jonathan B, Laberge, Anne-Marie, Little, Julian, Mhanni, Aizeddin, Mitchell, John J, Nakhla, Meranda, Potter, Murray, Prasad, Chitra, Rockman-Greenberg, Cheryl, Sparkes, Rebecca, Stockler, Sylvia, Ueda, Keiko, Vallance, Hilary, Wilson, Brenda J, Chakraborty, Pranesh, Potter, Beth K

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The health system impact of false positive newborn screening results for medium-chain acyl-CoA dehydrogenase deficiency: a cohort study von Karaceper, Maria D, Chakraborty, Pranesh, Coyle, Doug, Wilson, Kumanan, Kronick, Jonathan B, Hawken, Steven, Davies, Christine, Brownell, Marni, Dodds, Linda, Feigenbaum, Annette, Fell, Deshayne B, Grosse, Scott D, Guttmann, Astrid, Laberge, Anne-Marie, Mhanni, Aizeddin, Miller, Fiona A, Mitchell, John J, Nakhla, Meranda, Prasad, Chitra, Rockman-Greenberg, Cheryl, Sparkes, Rebecca, Wilson, Brenda J, Potter, Beth K

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Achieving the “triple aim” for inborn errors of metabolism: a review of challenges to outcomes research and presentation of a new practice-based evidence framework von Potter, Beth K., Chakraborty, Pranesh, Kronick, Jonathan B., Wilson, Kumanan, Coyle, Doug, Feigenbaum, Annette, Geraghty, Michael T., Karaceper, Maria D., Little, Julian, Mhanni, Aizeddin, Mitchell, John J., Siriwardena, Komudi, Wilson, Brenda J., Syrowatka, Ania

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Scoping review of patient- and family-oriented outcomes and measures for chronic pediatric disease von Khangura, Sara D, Karaceper, Maria D, Trakadis, Yannis, Mitchell, John J, Chakraborty, Pranesh, Tingley, Kylie, Coyle, Doug, Grosse, Scott D, Kronick, Jonathan B, Laberge, Anne-Marie, Little, Julian, Prasad, Chitra, Sikora, Lindsey, Siriwardena, Komudi, Sparkes, Rebecca, Speechley, Kathy N, Stockler, Sylvia, Wilson, Brenda J, Wilson, Kumanan, Zayed, Reem, Potter, Beth K

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THE EPIDEMIOLOGY AND HEALTH SYSTEM IMPACT OF MEDIUM-CHAIN ACYL-COA DEHYDROGENASE DEFICIENCY AMONG AFFECTED CHILDREN AND THOSE WITH FALSE POSITIVE NEWBORN SCREENING RESULTS IN ONTAR... von Karaceper, Maria D, Chakraborty, Pranesh, Coyle, Doug, Wilson, Kumanan, Potter, Beth K

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Patient- and family-oriented outcomes for inborn errors of metabolism: A scoping review von Khangura, Sara D., Chakraborty, Pranesh, Coyle, Doug, Karaceper, Maria D., Kronick, Jonathan B., Laberge, Anne-Marie, Little, Julian, Miller, Fiona, Mitchell, John J., Prasad, Chitra, Siriwardena, Komudi, Sparkes, Rebecca, Speechley, Kathy N., Stockler, Sylvia, Tingley, Kylie, Trakadis, Yannis, Wilson, Brenda, Wilson, Kumanan, Zayed, Reem, Potter, Beth K.

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The epidemiology and health service impact of medium-chain acyl-CoA dehydrogenase deficiency among affected children and those with false positive newborn screening results in Onta... von Karaceper, Maria D., Brownell, Marni, Casey, Robin, Chakraborty, Pranesh, Coyle, Doug, Dodds, Linda, Feigenbaum, Annette, Fell, Deshayne, Grosse, Scott, Guttmann, Astrid, Laberge, Anne-Marie, Mhanni, Aziz, Miller, Fiona, Nakhla, Meranda, Rockman-Greenberg, Cheryl, Sparkes, Rebecca, Vallance, Hilary, Wilson, Brenda, Wilson, Kumanan, Potter, Beth K.

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An examination of sex differences in associations between cord blood adipokines and childhood adiposity von Ashley‐Martin, Jillian, Karaceper, Maria, Dodds, Linda, Arbuckle, Tye E., Ettinger, Adrienne S., Fraser, William D., Muckle, Gina, Monnier, Patricia, Fisher, Mandy, Kuhle, Stefan

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Building a pan-Canadian practice-based research network for inherited metabolic diseases: The first two years of the Canadian Inherited Metabolic Diseases Research Network (CIMDRN) von Potter, Beth K., Chakraborty, Pranesh, Coyle, Doug, Kronick, Jonathan B., Wilson, Kumanan, Brownell, Marni, Chan, Alicia, Dodd, Linda, Dyack, Sarah, Feigenbaum, Annette, Fell, Deshayne, Geraghty, Michael T., Gillis, Jane, Rockman-Greenberg, Cheryl, Guttmann, Astrid, Hernandez, Monica, Karaceper, Maria, Khan, Aneal, Khangura, Sara D., Laberge, Anne-Marie, Little, Julian, MacKenzie, Jennifer, Maranda, Bruno, Mhanni, Aizeddin, Miller, Fiona A., Mitchell, John J., Mitchell, Grant, Nakhla, Meranda, Potter, Murray, Prasad, Chitra, Siriwardena, Komudi, Sparkes, Rebecca, Speechley, Kathy N., Stockler, Sylvia, Tingley, Kylie, Trakadis, Yannis, Turner, Lesley, Vallance, Hilary, van Karnebeek, Clara, Wilson, Brenda J., Yuskiv, Nataliya

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