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Epileptic Disorders : International Epilepsy Journal with Videotape|September 14, 2016
Myoclonus epilepsy in mitochondrial disordersCostanza Lamperti, Massimo ZevianiNeuromuscular Disorders : NMD|January 10, 2012
Partial tandem duplication of mtDNA-tRNA(Phe) impairs mtDNA translation in late-onset mitochondrial myopathyPaola Arzuffi, Costanza Lamperti, Erika Fernandez-Vizarra, et al.EMBO Molecular Medicine|August 21, 2012
Effective AAV-mediated gene therapy in a mouse model of ethylmalonic encephalopathyIvano Di Meo, Alberto Auricchio, Costanza Lamperti, et al.Neuromuscular Disorders : NMD|July 27, 2012
MELAS-like encephalomyopathy caused by a new pathogenic mutation in the mitochondrial DNA encoded cytochrome c oxidase subunit ICostanza Lamperti, Daria Diodato, Eleonora Lamantea, et al.Nature Medicine|July 27, 2010
Combined treatment with oral metronidazole and N-acetylcysteine is effective in ethylmalonic encephalopathyCarlo Viscomi, Alberto B Burlina, Imad Dweikat, et al.Human Mutation|September 10, 2013
A homozygous mutation in LYRM7/MZM1L associated with early onset encephalopathy, lactic acidosis, and severe reduction of mitochondrial complex III activityFederica Invernizzi, Marco Tigano, Cristina Dallabona, et al.EMBO Molecular Medicine|October 13, 2018
Rapamycin rescues mitochondrial myopathy via coordinated activation of autophagy and lysosomal biogenesisGabriele Civiletto, Sukru Anil Dogan, Raffaele Cerutti, et al.Cell Metabolism|July 5, 2011
In vivo correction of COX deficiency by activation of the AMPK/PGC-1α axisCarlo Viscomi, Emanuela Bottani, Gabriele Civiletto, et al.Cell Metabolism|June 4, 2015
Opa1 overexpression ameliorates the phenotype of two mitochondrial disease mouse modelsGabriele Civiletto, Tatiana Varanita, Raffaele Cerutti, et al.American Journal of Human Genetics|April 6, 2010
Severe X-linked mitochondrial encephalomyopathy associated with a mutation in apoptosis-inducing factorDaniele Ghezzi, Irina Sevrioukova, Federica Invernizzi, et al.Pageof 36