David Gustav Erik Olsson

Artiklar

Article: JIMD REPORTS. 2022;63(2):181-190
Very long-chain acyl-CoA dehydrogenase deficiency in a Swedish cohort: Clinical symptoms, newborn screening, enzyme activity, and genetics.
Olsson D; Barbaro M; Haglind C; Halldin M; Lajic S; Tucci S; Zetterström RH; Nordenström A
Article: CLINICAL AND TRANSLATIONAL SCIENCE. 2022;15(1):182-194
Altered mitochondrial metabolism in peripheral blood cells from patients with inborn errors of β-oxidation
Stenlid R; Olsson D; Cen J; Manell H; Haglind C; Chowdhury AI; Bergsten P; Nordenstrom A; Halldin M
Article: ACTA PAEDIATRICA, INTERNATIONAL JOURNAL OF PAEDIATRICS. 2016;105(12):1451-1460
Most patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency develop pathological or subnormal retinal function
Fahnehjelm KT; Liu Y; Olsson D; Amren U; Haglind CB; Holmstrom G; Halldin M; Andreasson S; Nordenstrom A