J. McNulty

Glutaric aciduria type 1: Diagnosis, clinical features and long‐term outcome in a large cohort of 34 Irish patients

I. Knerr, E. Crushell, E. Treacy, 2022, JIMD reports.

Growth Patterns in the Irish Pyridoxine Nonresponsive Homocystinuria Population and the Influence of Metabolic Control and Protein Intake

I. Knerr, A. Coughlan, E. Crushell, 2017, Journal of nutrition and metabolism.

Guidelines for the diagnosis and management of cystathionine beta-synthase deficiency

I. T. de Almeida, H. Blom, M. Hochuli, 2016, Journal of Inherited Metabolic Disease.

Organic Aciduria Disorders in Pregnancy: An Overview of Metabolic Considerations

E. Treacy, L. Shakerdi, B. Gillman, 2023, Metabolites.

Assessment of Dietary Intake of Iodine and Risk of Iodine Deficiency in Children with Classical Galactosaemia on Dietary Treatment

I. Knerr, J. McNulty, Dearbhla Milner, 2023, Nutrients.

Management of pregnancy in a patient with long‐chain 3‐hydroxyacyl CoA dehydrogenase deficiency

E. Treacy, J. Donnelly, C. McCarthy, 2022, JIMD reports.

The challenges of pregnancy management in pyridoxine nonresponsive homocystinuria: The Irish experience

E. Crushell, M. Cotter, C. Hart, 2021, JIMD reports.