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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 16, 2004
Analysis of the mitochondrial encoded subunits of complex I in 20 patients with a complex I deficiencyAnn Meulemans, Willy Lissens, Rudy Van Coster, et al.
Archives of Neurology|August 16, 2006
A novel mitochondrial transfer RNA(Asn) mutation causing multiorgan failureAnn Meulemans, Sara Seneca, Lieven Lagae, et al.
Clinical Genetics|December 19, 2020
Phenotypic spectrum of the RBM10-mediated intellectual disability and congenital malformation syndrome beyond classic TARP syndrome featuresCandy Kumps, Erika D'haenens, Sarah Vergult, et al.
Motor Control|July 28, 2006
Differences in gait between children with and without developmental coordination disorderFrederik J A Deconinck, Dirk De Clercq, Geert J P Savelsbergh, et al.
Archives of Neurology|September 12, 2007
Two novel mitochondrial DNA mutations in muscle tissue of a patient with limb-girdle myopathyAnn Meulemans, Boel De Paepe, Jan De Bleecker, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|September 9, 2020
Mild myopathic phenotype in a patient with homozygous c.416C > T mutation in <i>TK2</i> geneGeorge K Papadimas, Efthimia Vargiami, Pinelopi Dragoumi, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 28, 2014
Lambert-Eaton myasthenic syndrome in a 13-year-old girl with Xp11.22-p11.23 duplicationSabine Verbeek, Olivier Vanakker, Rudy Mercelis, et al.
Mitochondrion|June 29, 2010
Characterization of complex III deficiency and liver dysfunction in GRACILE syndrome caused by a BCS1L mutationHeike Kotarsky, Riitta Karikoski, Matthias Mörgelin, et al.
Mitochondrion|June 24, 2014
Mitochondrial encephalomyopathy with cytochrome c oxidase deficiency caused by a novel mutation in the MTCO1 geneFrançois-Guillaume Debray, Sara Seneca, Michel Gonce, et al.
Muscle & Nerve|July 19, 2012
Proteomic analysis in giant axonal neuropathy: new insights into disease mechanismsSilke Mussche, Boel De Paepe, Joél Smet, et al.
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