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Acta Clinica Belgica|November 10, 2006
Streptococcus cristatus isolated from a resected heart valve and blood cultures: case reports and application of phenotypic and genotypic techniques for identificationCharlotte Matthys, Geert Claeys, Gerda Verschraegen, et al.
Neurology. Genetics|December 21, 2018
Leigh syndrome followed by parkinsonism in an adult with homozygous c.626C>T mutation in <i>MTFMT</i>Dimitri M Hemelsoet, Arnaud V Vanlander, Joél Smet, et al.
Cell Reports|November 10, 2015
Cellular Heterogeneity in the Level of mtDNA Heteroplasmy in Mouse Embryonic Stem CellsJitesh Neupane, Sabitri Ghimire, Mado Vandewoestyne, et al.
Phytotherapy Research : PTR|April 27, 2013
Effect of resveratrol on cultured skin fibroblasts from patients with oxidative phosphorylation defectsBoel De Paepe, Katrien Vandemeulebroecke, Joél Smet, et al.
Annals of Neurology|August 10, 2010
Mutations in PEX10 are a cause of autosomal recessive ataxiaLuc Régal, Merel S Ebberink, Nathalie Goemans, et al.
Mitochondrion|September 18, 2014
Assessment of nuclear transfer techniques to prevent the transmission of heritable mitochondrial disorders without compromising embryonic development competence in miceJitesh Neupane, Mado Vandewoestyne, Sabitri Ghimire, et al.
Mitochondrion|August 28, 2014
Mutation-free baby born from a mitochondrial encephalopathy, lactic acidosis and stroke-like syndrome carrier after blastocyst trophectoderm preimplantation genetic diagnosisBjörn Heindryckx, Jitesh Neupane, Mado Vandewoestyne, et al.
Human Gene Therapy|January 16, 2013
Restoration of cytoskeleton homeostasis after gigaxonin gene transfer for giant axonal neuropathySilke Mussche, Bart Devreese, Sahana Nagabhushan Kalburgi, et al.
Pediatric Research|June 26, 2012
Fluorescence imaging of mitochondria in cultured skin fibroblasts: a useful method for the detection of oxidative phosphorylation defectsBoel De Paepe, Joél Smet, Arnaud Vanlander, et al.
American Journal of Medical Genetics. Part A|August 12, 2003
Clinical and diagnostic characteristics of complex III deficiency due to mutations in the BCS1L geneLinda De Meirleir, Sara Seneca, Eliane Damis, et al.
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