Amy Pender
Hamilton, ON, Canada
Last Updated: 09/26/2026
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Found 8 publications
The impacts of caring for children with inherited metabolic diseases for families: a cross-sectional study.
Journal: Orphanet journal of rare diseases
Published: December 09, 2025
Metabolic Control and Frequency of Clinical Monitoring Among Canadian Children With Phenylalanine Hydroxylase Deficiency: A Retrospective Cohort Study.
Journal: JIMD reports
Published: June 09, 2025
Family-centred care interventions for children with chronic conditions: A scoping review.
Journal: Health expectations : an international journal of public participation in health care and health policy
Published: June 30, 2023
Assessing the quality and value of metabolic chart data for capturing core outcomes for pediatric medium-chain acyl-CoA dehydrogenase (MCAD) deficiency.
Journal: BMC pediatrics
Published: May 19, 2023
Evaluation of the quality of clinical data collection for a pan-Canadian cohort of children affected by inherited metabolic diseases: lessons learned from the Canadian Inherited Metabolic Diseases Research Network.
Journal: Orphanet journal of rare diseases
Published: December 09, 2019
Nutritional management of phenylalanine hydroxylase (PAH) deficiency in pediatric patients in Canada: a survey of dietitians' current practices.
Journal: Orphanet journal of rare diseases
Published: July 09, 2018
Recommendations for the use of sapropterin in phenylketonuria.
Journal: Molecular genetics and metabolism
Published: March 09, 2012
Showing 1-8 of 8
Last Updated: 09/26/2026