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American Journal of Medical Genetics. Part A|June 10, 2003
Homozygous Gly555Glu mutation in the nuclear-encoded 70 kDa flavoprotein gene causes instability of the respiratory chain complex IIRudy Van Coster, S Seneca, J Smet, et al.Neuropediatrics|August 23, 2007
Ethylmalonic encephalopathy: clinical and biochemical observationsD I Zafeiriou, P Augoustides-Savvopoulou, D Haas, et al.Pediatric Research|October 20, 2001
Blue native polyacrylamide gel electrophoresis: a powerful tool in diagnosis of oxidative phosphorylation defectsR Van Coster, J Smet, E George, et al.Neuromuscular Disorders : NMD|October 21, 2006
Deficiency of mitochondrial ATP synthase of nuclear genetic originW Sperl, P Jesina, J Zeman, et al.Genetic Counseling (Geneva, Switzerland)|February 28, 2018
Mitochondrial Neurogastrointestinal Encephalopathy: Clinical, Biochemical and Molecular Study in Three Egyptian PatientsL Selim, R Van Coster, D Mehaney, et al.Acta Anaesthesiologica Scandinavica|January 21, 2012
Inborn oxidative phosphorylation defect as risk factor for propofol infusion syndromeA V Vanlander, P G Jorens, J Smet, et al.Journal of Neurology, Neurosurgery, and Psychiatry|December 19, 2009
Progressive myoclonic epilepsy as an adult-onset manifestation of Leigh syndrome due to m.14487T>CB Dermaut, S Seneca, L Dom, et al.Pageof 3