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Alette Giezen

University of British Columbia

11

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79

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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.

2020 Orphanet Journal of Rare Diseases
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Nutritional management of phenylalanine hydroxylase (PAH) deficiency in pediatric patients in Canada: a survey of dietitians’ current practices

2019 Orphanet Journal of Rare Diseases
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The Indicator Amino Acid Oxidation Method with the Use of L-[1-13C]Leucine Suggests a Higher than Currently Recommended Protein Requirement in Children with Phenylketonuria

2017 Journal of Nutrition
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Minimally invasive 13C-breath test to examine phenylalanine metabolism in children with phenylketonuria

2015 Molecular Genetics and Metabolism
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Individualized long-term outcomes in blood phenylalanine concentrations and dietary phenylalanine tolerance in 11 patients with primary phenylalanine hydroxylase (PAH) deficiency treated with Sapropterin-dihydrochloride

2015 Molecular Genetics and Metabolism
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Long-term outcomes of blood phenylalanine concentrations in children with classical phenylketonuria

2013 Molecular Genetics and Metabolism
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