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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.
JIMD Reports|September 3, 2025
Metabolic Control and Frequency of Clinical Monitoring Among Canadian Children With Phenylalanine Hydroxylase Deficiency: A Retrospective Cohort StudyNataliya Yuskiv, Ammar Saad, Beth K Potter, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 17, 2024
Implementing evidence-based assertions of clinical actionability in the context of secondary findings: Updates from the ClinGen Actionability Working GroupChristine M Pak, Marian J Gilmore, Joanna E Bulkley, 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.
Chest|October 26, 2017
Clinical Course of Sarcoidosis in World Trade Center-Exposed FirefightersKerry M Hena, Jennifer Yip, Nadia Jaber, et al.
JAMA Oncology|May 1, 2018
Multiple Myeloma and Its Precursor Disease Among Firefighters Exposed to the World Trade Center DisasterOla Landgren, Rachel Zeig-Owens, Orsolya Giricz, et al.
Health Expectations : an International Journal of Public Participation in Health Care and Health Policy|August 5, 2024
Family-centred care interventions for children with chronic conditions: A scoping reviewAndrea J Chow, Ammar Saad, Zobaida Al-Baldawi, et al.
Orphanet Journal of Rare Diseases|January 16, 2020
Outcomes in pediatric studies of medium-chain acyl-coA dehydrogenase (MCAD) deficiency and phenylketonuria (PKU): a reviewMichael Pugliese, Kylie Tingley, Andrea Chow, et al.
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