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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 13, 2006
A new family with the mitochondrial tRNAGLU gene mutation m.14709T>C presenting with hydrops fetalisAnn Meulemans, Sara Seneca, Joel Smet, et al.Molecular Genetics and Metabolism|May 29, 2016
Evidence of a wide spectrum of cardiac involvement due to ACAD9 mutations: Report on nine patientsJoseph P Dewulf, Catherine Barrea, Marie-Françoise Vincent, et al.Electrophoresis|October 29, 2009
Subcomplexes of mitochondrial complex V reveal mutations in mitochondrial DNAJoél Smet, Sara Seneca, Boel De Paepe, et al.American Journal of Medical Genetics. Part A|August 2, 2005
A mitochondrial tRNA aspartate mutation causing isolated mitochondrial myopathySara Seneca, Nathalie Goemans, Rudy Van Coster, et al.Journal of Child Neurology|July 19, 2013
Uncommon Leber "plus" disease associated with mitochondrial mutation m.11778G>A in a premature childStéphanie Paquay, Valérie Benoit, Catherine Wetzburger, et al.Adapted Physical Activity Quarterly : APAQ|January 23, 2008
Sensory contributions to balance in boys with developmental coordination disorderFrederik J A Deconinck, Dirk De Clercq, Rudy Van Coster, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 1, 2008
Vagus nerve stimulation for refractory status epilepticusVeerle De Herdt, Liesbeth Waterschoot, Kristl Vonck, et al.Respiratory Physiology & Neurobiology|September 28, 2013
Forearm muscle oxygenation responses during and following arterial occlusion in patients with mitochondrial myopathyJan Boone, Bert Celie, Jasmien Dumortier, et al.Orphanet Journal of Rare Diseases|May 23, 2018
Severe hepatopathy and neurological deterioration after start of valproate treatment in a 6-year-old child with mitochondrial tryptophanyl-tRNA synthetase deficiencyElise Vantroys, Joél Smet, Arnaud V Vanlander, et al.European Journal of Human Genetics : EJHG|March 27, 2014
Analysis of the whole mitochondrial genome: translation of the Ion Torrent Personal Genome Machine system to the diagnostic bench?Sara Seneca, Kim Vancampenhout, Rudy Van Coster, et al.Pageof 13