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Systematic Reviews|January 13, 2021
Screening for depression in children and adolescents: a protocol for a systematic review updateAndrew Beck, John C LeBlanc, Kate Morissette, et al.
The Patient|July 20, 2021
Family Experiences with Care for Children with Inherited Metabolic Diseases in Canada: A Cross-Sectional SurveyAndrea J Chow, Michael Pugliese, Laure A Tessier, et al.
Orphanet Journal of Rare Diseases|December 9, 2016
Experiences of caregivers of children with inherited metabolic diseases: a qualitative studyShabnaz Siddiq, Brenda J Wilson, Ian D Graham, et al.
JIMD Reports|February 27, 2015
Metabolic Clinic Atlas: Organization of Care for Children with Inherited Metabolic Disease in CanadaMonica F Lamoureux, Kylie Tingley, Jonathan B Kronick, et al.
Orphanet Journal of Rare Diseases|March 24, 2019
Health services use among children diagnosed with medium-chain acyl-CoA dehydrogenase deficiency through newborn screening: a cohort study in Ontario, CanadaMaria D Karaceper, Sara D Khangura, Kumanan Wilson, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|August 8, 2019
Health Care for Mitochondrial Disorders in Canada: A Survey of PhysiciansKaren Paik, Matthew A Lines, Pranesh Chakraborty, et al.
Orphanet Journal of Rare Diseases|June 11, 2026
The impacts of caring for children with inherited metabolic diseases for families: a cross-sectional studyAndrea J Chow, Isabel Jordan, Nicole Pallone, et al.
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