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Massimo Zeviani

Showing results (31-40 of 289) with videos related to

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Current Opinion in Genetics & Development|June 6, 2003
Nuclear genes in mitochondrial disordersMassimo Zeviani, Antonella Spinazzola, Valerio Carelli
Molecular Genetics and Metabolism Reports|September 14, 2020
Ethylmalonic encephalopathy: Clinical course and therapy response in an uncommon mild case with a severe ETHE1 mutationMelike Ersoy, Valeria Tiranti, Massimo Zeviani
Biochimica Et Biophysica Acta|March 14, 2015
Emerging concepts in the therapy of mitochondrial diseaseCarlo Viscomi, Emanuela Bottani, Massimo Zeviani
Biochimica Et Biophysica Acta|July 16, 2008
Assembly of the oxidative phosphorylation system in humans: what we have learned by studying its defectsErika Fernández-Vizarra, Valeria Tiranti, Massimo Zeviani
Handbook of Clinical Neurology|August 11, 2011
Ataxia in mitochondrial disordersMassimo Zeviani, Alessandro Simonati, Laurence A Bindoff
Annals of Neurology|January 10, 2002
MRI in Leigh syndrome with SURF1 gene mutationMario Savoiardo, Massimo Zeviani, Graziella Uziel, et al.
Neuromuscular Disorders : NMD|February 12, 2008
Lack of founder effect for an identical mtDNA depletion syndrome (MDS)-associated MPV17 mutation shared by Navajos and ItaliansAntonella Spinazzola, Valeria Massa, Michio Hirano, et al.
Frontiers in Genetics|February 22, 2020
RNase H1 Regulates Mitochondrial Transcription and Translation <i>via</i> the Degradation of 7S RNAAurelio Reyes, Joanna Rusecka, Katarzyna Tońska, et al.
Biochimica Et Biophysica Acta|June 16, 2009
The R336Q mutation in human mitochondrial EFTu prevents the formation of an active mt-EFTu.GTP.aa-tRNA ternary complexLucia Valente, Narumi Shigi, Tsutomu Suzuki, et al.
Mitochondrion|February 7, 2007
Depletion of mtDNA: syndromes and genesSimona Alberio, Rossana Mineri, Valeria Tiranti, et al.
Pageof 29

Showing results (31-40 of 289) with videos related to

Sort By:
Pageof 29
Current Opinion in Genetics & Development|June 6, 2003
Nuclear genes in mitochondrial disordersMassimo Zeviani, Antonella Spinazzola, Valerio Carelli
Molecular Genetics and Metabolism Reports|September 14, 2020
Ethylmalonic encephalopathy: Clinical course and therapy response in an uncommon mild case with a severe ETHE1 mutationMelike Ersoy, Valeria Tiranti, Massimo Zeviani
Biochimica Et Biophysica Acta|March 14, 2015
Emerging concepts in the therapy of mitochondrial diseaseCarlo Viscomi, Emanuela Bottani, Massimo Zeviani
Biochimica Et Biophysica Acta|July 16, 2008
Assembly of the oxidative phosphorylation system in humans: what we have learned by studying its defectsErika Fernández-Vizarra, Valeria Tiranti, Massimo Zeviani
Handbook of Clinical Neurology|August 11, 2011
Ataxia in mitochondrial disordersMassimo Zeviani, Alessandro Simonati, Laurence A Bindoff
Annals of Neurology|January 10, 2002
MRI in Leigh syndrome with SURF1 gene mutationMario Savoiardo, Massimo Zeviani, Graziella Uziel, et al.
Neuromuscular Disorders : NMD|February 12, 2008
Lack of founder effect for an identical mtDNA depletion syndrome (MDS)-associated MPV17 mutation shared by Navajos and ItaliansAntonella Spinazzola, Valeria Massa, Michio Hirano, et al.
Frontiers in Genetics|February 22, 2020
RNase H1 Regulates Mitochondrial Transcription and Translation <i>via</i> the Degradation of 7S RNAAurelio Reyes, Joanna Rusecka, Katarzyna Tońska, et al.
Biochimica Et Biophysica Acta|June 16, 2009
The R336Q mutation in human mitochondrial EFTu prevents the formation of an active mt-EFTu.GTP.aa-tRNA ternary complexLucia Valente, Narumi Shigi, Tsutomu Suzuki, et al.
Mitochondrion|February 7, 2007
Depletion of mtDNA: syndromes and genesSimona Alberio, Rossana Mineri, Valeria Tiranti, et al.
Pageof 29