Mei 2016
30
7 Literatuurlijst
Ahn MS, Sims KB, Frazier JA. 2005. Risperidone-induced psychosis and depression in a child with a
mitochondrial disorder. J Child Adolesc Psychopharmacol 15: 520-5.
Barkovich J, Raybaud C. Pediatric Neuroimaging. 2012. 5th Edition.
Brunmair B, Staniek K, Gras F, Scharf N, Althaym A, Clara R, Roden M, Gnaiger E, Nohl H, Waldhäusl
W, Fürnsinn C. 2004. Thiazolidinediones, like metformin, inhibit respiratory complex I: a common
mechanism contributing to their antidiabetic actions? Diabetes 53: 1052-9.
Carvalho C, Correia S, Santos MS, Seiça R, Oliveira CR, Moreira PI. 2008. Metformin promotes
isolated rat liver mitochondria impairment. Mol Cell Biochem 308: 75-83.
Casademont J, Garrabou G, Miró O, López S, Pons A, Bernardo M, Cardellach F. 2007. Neuroleptic
treatment effect on mitochondrial electron transport chain: peripheral blood mononuclear cells
analysis in psychotic patients. J Clin Psychipharmacol 27: 284-8.
Clarke C, Xiao R, Place E, Zhang Z, Sondheimer N, Bennett M, Yudkoff M, Falk MJ.
Mitochondrial respiratory chain disease discrimination by retrospective cohort analysis of blood
metabolites. 2013. Mol Genet Metab 110:145-52.
De Stefano N, Matthews PM, Ford B, Genge A, Karpati G, Arnold DL. Short-term dichloroacetate
treatment improves indices of cerebral metabolism in patients with mitochondrial disorders. 1995.
Neurology 45:1193-1198
Distelmaier F, Huppke P, Pieperhoff P, Amunts K, Schaper J, Morava E, Mayatepek E, Kohlhase J,
Karenfort M. 2013. Biotin-Responsive Basal Ganglia Disease: A Treatable Differential Diagnosis of
Leigh Syndrome. Case Res Rep 13: 53-57
Elisa Fassone, Shamina Rahman. 2012. Complex I deficiency: clinical features, biochemistry and
molecular genetics. J Med Genet 49:578-590
Finsterer J, Segall L. 2010. Drugs interfering with mitochondrial disorders. Drug Chem Toxicol
33:138-51
Fraser JL, Vanderver A, Yang S, Chang T, Cramp L, Vezinae G. 2014. Thiamine pyrophosphokinase
deficiency causes a Leigh Disease like phenotype in a sibling pair: identification through whole
exome sequencing and management strategies
Mol Gen Metabol Rep: 66–70
Fromenty B, Pessayre D. 1995 Inhibition of mitochondrial beta-oxidation as a mechanism of
hepatotoxicity. Pharmacol Ther 67:101-54.
Gerards M, Kamps R, van Oevelen J, Boesten I, Jongen E, de Koning B, Scholte HR, de Angst I,
Schoonderwoerd K, Sefiani A, Ratbi I, Coppieters W, Karim L, de Coo R, van den Bosch B, Smeets H.
Exome sequencing reveals a novel Moroccan founder mutation in SLC19A3 as a new cause of early-
childhood fatal Leigh syndrome. Brain. 2013;136(Pt 3):882-90.
