J. G. Okun

发表

Possible Pathogenic Mechanism of Propofol Infusion Syndrome Involves Coenzyme Q

G. Dacremont, P. Jorens, N. Van Regenmortel, 2015, Anesthesiology.

Inborn oxidative phosphorylation defect as risk factor for propofol infusion syndrome

S. Seneca, G. G. Van den Eynden, P. Jorens, 2012, Acta anaesthesiologica Scandinavica.

Impact of short- and medium-chain organic acids, acylcarnitines, and acyl-CoAs on mitochondrial energy metabolism.

G. Hoffmann, S. Sauer, M. Morath, 2008, Biochimica et biophysica acta.

Pathogenesis of CNS involvement in disorders of amino and organic acid metabolism

S. Kölker, S. Sauer, M. Morath, 2008, Journal of Inherited Metabolic Disease.

Methylmalonic acid — an endogenous toxin?

S. Kölker, J. G. Okun, 2005, Cellular and Molecular Life Sciences.

Neurodegeneration and chronic renal failure in methylmalonic aciduria—A pathophysiological approach

S. Kölker, J. Okun, G. Hoffmann, 2008, Journal of Inherited Metabolic Disease.

Crystal structure and interaction studies of human DHTKD1 provide insight into a mitochondrial megacomplex in lysine catabolism

G. A. Bezerra, W. Yue, J. Rutter, 2020, bioRxiv.

Coenzyme Q10 is decreased in fibroblasts of patients with methylmalonic aciduria but not in mevalonic aciduria

E. R. Baumgartner, R. Rodenburg, J. Okun, 2009, Journal of Inherited Metabolic Disease.

Erratum to: Long-term exposure of human proximal tubule cells to hydroxycobalamin[c-lactam] as a possible model to study renal disease in methylmalonic acidurias

S. Kölker, S. Sauer, S. Opp, 2009, Journal of Inherited Metabolic Disease.

Long-term exposure of human proximal tubule cells to hydroxycobalamin[c-lactam] as a possible model to study renal disease in methylmalonic acidurias

S. Kölker, S. Sauer, S. Opp, 2009, Journal of Inherited Metabolic Disease.

Animal models for glutaryl-CoA dehydrogenase deficiency

M. Wajner, S. Kölker, C. Mühlhausen, 2004, Journal of Inherited Metabolic Disease.

Excitotoxicity and bioenergetics in glutaryl-CoA dehydrogenase deficiency

S. Kölker, J. Okun, G. Hoffmann, 2004, Journal of Inherited Metabolic Disease.

Possible Pathogenic Mechanism of Propofol Infusion Syndrome Involves Coenzyme Q

G. Dacremont, P. Jorens, N. Van Regenmortel, 2015, Anesthesiology.

Newborn screening for homocystinurias: recent recommendations versus current practice

M. Baumgartner, H. Blom, A. Ribes, 2018, Journal of Inherited Metabolic Disease.