Health services use by children identified as heterozygous hemoglobinopathy mutation carriers via newborn screening

द्वारा 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
में प्रकाशित BMC Pediatr (2021)

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

द्वारा 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
प्रकाशित 2013

Scoping review of patient- and family-oriented outcomes and measures for chronic pediatric disease

द्वारा 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
में प्रकाशित BMC Pediatr (2015)

The health system impact of false positive newborn screening results for medium-chain acyl-CoA dehydrogenase deficiency: a cohort study

द्वारा 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.
में प्रकाशित Orphanet J Rare Dis (2016)

Health services use among children diagnosed with medium-chain acyl-CoA dehydrogenase deficiency through newborn screening: a cohort study in Ontario, Canada

द्वारा 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.
में प्रकाशित Orphanet J Rare Dis (2019)