Jonathan B. Kronick

555 University Avenue
Toronto, ON, Canada

Last Updated: 09/26/2026

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Found 24 publications

Metabolic Control and Frequency of Clinical Monitoring Among Canadian Children With Phenylalanine Hydroxylase Deficiency: A Retrospective Cohort Study.

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

Assessing the quality and value of metabolic chart data for capturing core outcomes for pediatric medium-chain acyl-CoA dehydrogenase (MCAD) deficiency.

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

Organic Acidemias.

Organic Acidemias.

Journal: Pediatrics in review

Published: March 01, 2022

Family Experiences with Care for Children with Inherited Metabolic Diseases in Canada: A Cross-Sectional Survey.

Family Experiences with Care for Children with Inherited Metabolic Diseases in Canada: A Cross-Sectional Survey.

Journal: The patient

Published: June 29, 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

Development of infantile tremor syndrome after initiation of hydroxycobalamin treatment in an infant with a late diagnosis of cobalamin C disorder.

Development of infantile tremor syndrome after initiation of hydroxycobalamin treatment in an infant with a late diagnosis of cobalamin C disorder.

Journal: JIMD reports

Published: February 03, 2020

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.

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

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

Health Care for Mitochondrial Disorders in Canada: A Survey of Physicians.

Health Care for Mitochondrial Disorders in Canada: A Survey of Physicians.

Journal: The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques

Published: August 08, 2019

Excellence in clinical care is the most important thing, but not the only thing.

Excellence in clinical care is the most important thing, but not the only thing.

Journal: Paediatrics & child health

Published: February 23, 2019

Health services use among children diagnosed with medium-chain acyl-CoA dehydrogenase deficiency through newborn screening: a cohort study in Ontario, Canada.

Health services use among children diagnosed with medium-chain acyl-CoA dehydrogenase deficiency through newborn screening: a cohort study in Ontario, Canada.

Journal: Orphanet journal of rare diseases

Published: April 10, 2018

Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test.

Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: March 18, 2017

Showing 1-12 of 24

Last Updated: 09/26/2026