Nicole Pallone

Toronto, 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.

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

Youth and family involvement in the development of a plain language trial results communication tool: CommuniKIDS.

Youth and family involvement in the development of a plain language trial results communication tool: CommuniKIDS.

Journal: Research involvement and engagement

Published: June 08, 2023

Patient Engagement in a Multi-Stakeholder Workshop to Plan the Collection of Patient-Oriented Outcomes for Children with Inherited Metabolic Diseases.

Patient Engagement in a Multi-Stakeholder Workshop to Plan the Collection of Patient-Oriented Outcomes for Children with Inherited Metabolic Diseases.

Journal: Healthcare quarterly (Toronto, Ont.)

Published: April 25, 2022

Families' healthcare experiences for children with inherited metabolic diseases: protocol for a mixed methods cohort study.

Families' healthcare experiences for children with inherited metabolic diseases: protocol for a mixed methods cohort study.

Journal: BMJ open

Published: February 23, 2022

Patient and family engagement in the development of core outcome sets for two rare chronic diseases in children.

Patient and family engagement in the development of core outcome sets for two rare chronic diseases in children.

Journal: Research involvement and engagement

Published: May 11, 2021

Core Outcome Sets for Medium-Chain Acyl-CoA Dehydrogenase Deficiency and Phenylketonuria.

Core Outcome Sets for Medium-Chain Acyl-CoA Dehydrogenase Deficiency and Phenylketonuria.

Journal: Pediatrics

Published: March 22, 2021

Outcomes in pediatric studies of medium-chain acyl-coA dehydrogenase (MCAD) deficiency and phenylketonuria (PKU): a review.

Outcomes in pediatric studies of medium-chain acyl-coA dehydrogenase (MCAD) deficiency and phenylketonuria (PKU): a review.

Journal: Orphanet journal of rare diseases

Published: September 16, 2019

Establishing core outcome sets for phenylketonuria (PKU) and medium-chain Acyl-CoA dehydrogenase (MCAD) deficiency in children: study protocol for systematic reviews and Delphi surveys.

Establishing core outcome sets for phenylketonuria (PKU) and medium-chain Acyl-CoA dehydrogenase (MCAD) deficiency in children: study protocol for systematic reviews and Delphi surveys.

Journal: Trials

Published: August 23, 2017

Showing 1-8 of 8

Last Updated: 09/26/2026