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Journal of the American Heart Association|December 21, 2018
Elevated Inflammatory Plasma Biomarkers in Patients With Fabry Disease: A Critical Link to Heart Failure With Preserved Ejection FractionHaran Yogasundaram, Anish Nikhanj, Brendan N Putko, et al.
American Journal of Medical Genetics. Part A|November 19, 2022
Diagnostic yield of clinical exome sequencing in adulthood in medical genetics clinicsApurba Mainali, Taryn Athey, Shalini Bahl, 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.
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.
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.
Pediatrics|July 16, 2021
Core Outcome Sets for Medium-Chain Acyl-CoA Dehydrogenase Deficiency and PhenylketonuriaMichael Pugliese, Kylie Tingley, Andrea Chow, 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.
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