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Mitochondrion|April 19, 2011
Polar body mutation load analysis in a patient with A3243G tRNALeu(UUR) point mutationMado Vandewoestyne, Björn Heindryckx, Trees Lepez, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 10, 2010
Anti-NMDA-receptor encephalitis in a 3 year old patient with chromosome 6p21.32 microdeletion including the HLA clusterHelene Verhelst, Patrick Verloo, Karlien Dhondt, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 12, 2018
Recurrent arterial ischemic stroke with good response to mycophenolate mofetilBenedikte Van Driessche, Patrick Verloo, Nele Herregods, et al.Acta Neurologica Belgica|December 13, 2007
The aerobic forearm exercise test, a non-invasive tool to screen for mitochondrial disordersAnn Meulemans, Erik Gerlo, Sara Seneca, et al.Radiation Research|March 8, 2013
Unraveling the mechanisms behind the enhanced MTT conversion by irradiated breast cancer cellsStéphanie Blockhuys, Barbara Vanhoecke, Joél Smet, et al.European Journal of Pediatrics|July 11, 2014
Extremely high mutation load of the mitochondrial 8993 T>G mutation in a newborn: implications for prognosis and family planning decisionsClaudine De Praeter, Arnaud Vanlander, Piet Vanhaesebrouck, et al.European Journal of Medical Genetics|September 22, 2009
Challenges for CNV interpretation in clinical molecular karyotyping: lessons learned from a 1001 sample experienceKaren Buysse, Barbara Delle Chiaie, Rudy Van Coster, et al.Journal of Inherited Metabolic Disease|January 19, 2010
Aberrant synthesis of ATP synthase resulting from a novel deletion in mitochondrial DNA in an African patient with progressive external ophthalmoplegiaFrancois H van der Westhuizen, Joél Smet, Oksana Levanets, et al.Journal of Inherited Metabolic Disease|April 13, 2011
Complex III staining in blue native polyacrylamide gelsJoél Smet, Boel De Paepe, Sara Seneca, et al.American Journal of Medical Genetics. Part A|October 16, 2010
Giant axonal neuropathy caused by compound heterozygosity for a maternally inherited microdeletion and a paternal mutation within the GAN geneKaren Buysse, Sarah Vergult, Silke Mussche, et al.Pageof 13