C. Haglind

Increased and early lipolysis in children with long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency during fast

A. Nordenström, U. Döbeln, J. Gustafsson, 2015, Journal of Inherited Metabolic Disease.

Ocular characteristics in 10 children with long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency: a cross‐sectional study with long‐term follow‐up

A. Nordenström, G. Holmström, A. Németh, 2007, Acta ophthalmologica.

Energy metabolism and clinical symptoms in beta-oxidation defects, especially long-chain 3-hydroxyacyl-coenzyme a dehydrogenase deficiency

C. Haglind, 2016 .

Growth in Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency.

A. Nordenström, A. Németh, J. Alm, 2013, JIMD reports.

Altered mitochondrial metabolism in peripheral blood cells from patients with inborn errors of β‐oxidation

A. Nordenström, H. Manell, P. Bergsten, 2021, Clinical and translational science.

Neuropsychological Development in Patients with Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase (LCHAD) Deficiency.

A. Nordenström, A. Németh, R. Zetterström, 2015, JIMD reports.

Very long‐chain acyl‐CoA dehydrogenase deficiency in a Swedish cohort: Clinical symptoms, newborn screening, enzyme activity, and genetics

A. Nordenström, S. Lajic, M. Barbaro, 2022, JIMD reports.