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Massimo Zeviani

Showing results (151-160 of 289) with videos related to

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EMBO Molecular Medicine|December 15, 2012
The impairment of HCCS leads to MLS syndrome by activating a non-canonical cell death pathway in the brain and eyesAlessia Indrieri, Ivan Conte, Giancarlo Chesi, et al.
Nature Genetics|April 4, 2006
Systematic identification of human mitochondrial disease genes through integrative genomicsSarah Calvo, Mohit Jain, Xiaohui Xie, et al.
Nature Reviews. Disease Primers|October 25, 2016
Mitochondrial diseasesGráinne S Gorman, Patrick F Chinnery, Salvatore DiMauro, et al.
Molecular Genetics and Metabolism Reports|January 11, 2017
Pure myopathy with enlarged mitochondria associated to a new mutation in <i>MTND2</i> geneAlice Zanolini, Ana Potic, Franco Carrara, et al.
Nature Medicine|January 13, 2009
Loss of ETHE1, a mitochondrial dioxygenase, causes fatal sulfide toxicity in ethylmalonic encephalopathyValeria Tiranti, Carlo Viscomi, Tatjana Hildebrandt, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 29, 2020
Awareness of rare and genetic neurological diseases among italian neurologist. A national surveyMichelangelo Mancuso, Massimiliano Filosto, Costanza Lamperti, et al.
The Journal of Biological Chemistry|August 29, 2014
Leigh syndrome in Drosophila melanogaster: morphological and biochemical characterization of Surf1 post-transcriptional silencingCaterina Da-Rè, Sophia von Stockum, Alberto Biscontin, et al.
Plos Genetics|May 3, 2011
Evolution meets disease: penetrance and functional epistasis of mitochondrial tRNA mutationsRaquel Moreno-Loshuertos, Gustavo Ferrín, Rebeca Acín-Pérez, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 19, 2015
Clinical and genetic features of paroxysmal kinesigenic dyskinesia in Italian patientsCostanza Lamperti, Federica Invernizzi, Roberta Solazzi, et al.
Journal of Neurology|January 30, 2013
Adult-onset leukodystrophies from respiratory chain disorders: do they exist?Ettore Salsano, Laura Farina, Costanza Lamperti, et al.
Pageof 29

Showing results (151-160 of 289) with videos related to

Sort By:
Pageof 29
EMBO Molecular Medicine|December 15, 2012
The impairment of HCCS leads to MLS syndrome by activating a non-canonical cell death pathway in the brain and eyesAlessia Indrieri, Ivan Conte, Giancarlo Chesi, et al.
Nature Genetics|April 4, 2006
Systematic identification of human mitochondrial disease genes through integrative genomicsSarah Calvo, Mohit Jain, Xiaohui Xie, et al.
Nature Reviews. Disease Primers|October 25, 2016
Mitochondrial diseasesGráinne S Gorman, Patrick F Chinnery, Salvatore DiMauro, et al.
Molecular Genetics and Metabolism Reports|January 11, 2017
Pure myopathy with enlarged mitochondria associated to a new mutation in <i>MTND2</i> geneAlice Zanolini, Ana Potic, Franco Carrara, et al.
Nature Medicine|January 13, 2009
Loss of ETHE1, a mitochondrial dioxygenase, causes fatal sulfide toxicity in ethylmalonic encephalopathyValeria Tiranti, Carlo Viscomi, Tatjana Hildebrandt, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 29, 2020
Awareness of rare and genetic neurological diseases among italian neurologist. A national surveyMichelangelo Mancuso, Massimiliano Filosto, Costanza Lamperti, et al.
The Journal of Biological Chemistry|August 29, 2014
Leigh syndrome in Drosophila melanogaster: morphological and biochemical characterization of Surf1 post-transcriptional silencingCaterina Da-Rè, Sophia von Stockum, Alberto Biscontin, et al.
Plos Genetics|May 3, 2011
Evolution meets disease: penetrance and functional epistasis of mitochondrial tRNA mutationsRaquel Moreno-Loshuertos, Gustavo Ferrín, Rebeca Acín-Pérez, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 19, 2015
Clinical and genetic features of paroxysmal kinesigenic dyskinesia in Italian patientsCostanza Lamperti, Federica Invernizzi, Roberta Solazzi, et al.
Journal of Neurology|January 30, 2013
Adult-onset leukodystrophies from respiratory chain disorders: do they exist?Ettore Salsano, Laura Farina, Costanza Lamperti, et al.
Pageof 29