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DiMauro

Showing results (281-290 of 942) with videos related to

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Archives of Neurology|August 12, 2009
Human NARP mitochondrial mutation metabolism corrected with alpha-ketoglutarate/aspartate: a potential new therapyGianluca Sgarbi, Gabriella A Casalena, Alessandra Baracca, et al.
Plos One|July 15, 2020
Open-tES: An open-source stimulator for transcranial electrical stimulation designed for rodent researchSolène Pedron, Stéphanie Dumontoy, Julien Dimauro, et al.
Brain Pathology (Zurich, Switzerland)|April 1, 1992
Disorders associated with depletion of mitochondrial DNAE Ricci, C T Moraes, S Servidei, et al.
Growth Factors (Chur, Switzerland)|January 13, 2011
Modulation of the apoptotic pathway in skeletal muscle models: the role of growth hormoneIvan Dimauro, Fiorenza Magi, Gina La Sala, et al.
Journal of Child Neurology|September 17, 1999
A novel mutation in the mitochondrial DNA transfer ribonucleic acidAsp gene in a child with myoclonic epilepsy and psychomotor regressionA Shtilbans, M El-Schahawi, E Malkin, et al.
Biology of the Neonate|January 1, 1995
End-tidal carbon monoxide in newborn infants: observations during the 1st week of lifeV Balaraman, S Pelke, S DiMauro, et al.
Neurology|April 1, 1993
Polyglucosan body disease simulating amyotrophic lateral sclerosisT D McDonald, P L Faust, C Bruno, et al.
Archives of Neurology|March 11, 2009
Muscle phosphoglycerate mutase deficiency revisitedAli Naini, Antonio Toscano, Olimpia Musumeci, et al.
Neuromuscular Disorders : NMD|March 17, 2009
The m.3244G>A mutation in mtDNA is another cause of progressive external ophthalmoplegiaEvangelia Sotiriou, Jorida Coku, Kurenai Tanji, et al.
Physical Review Letters|June 1, 2004
Multiphoton double ionization via field-independent resonant excitationJ Rudati, J L Chaloupka, P Agostini, et al.
Pageof 95

Showing results (281-290 of 942) with videos related to

Sort By:
Pageof 95
Archives of Neurology|August 12, 2009
Human NARP mitochondrial mutation metabolism corrected with alpha-ketoglutarate/aspartate: a potential new therapyGianluca Sgarbi, Gabriella A Casalena, Alessandra Baracca, et al.
Plos One|July 15, 2020
Open-tES: An open-source stimulator for transcranial electrical stimulation designed for rodent researchSolène Pedron, Stéphanie Dumontoy, Julien Dimauro, et al.
Brain Pathology (Zurich, Switzerland)|April 1, 1992
Disorders associated with depletion of mitochondrial DNAE Ricci, C T Moraes, S Servidei, et al.
Growth Factors (Chur, Switzerland)|January 13, 2011
Modulation of the apoptotic pathway in skeletal muscle models: the role of growth hormoneIvan Dimauro, Fiorenza Magi, Gina La Sala, et al.
Journal of Child Neurology|September 17, 1999
A novel mutation in the mitochondrial DNA transfer ribonucleic acidAsp gene in a child with myoclonic epilepsy and psychomotor regressionA Shtilbans, M El-Schahawi, E Malkin, et al.
Biology of the Neonate|January 1, 1995
End-tidal carbon monoxide in newborn infants: observations during the 1st week of lifeV Balaraman, S Pelke, S DiMauro, et al.
Neurology|April 1, 1993
Polyglucosan body disease simulating amyotrophic lateral sclerosisT D McDonald, P L Faust, C Bruno, et al.
Archives of Neurology|March 11, 2009
Muscle phosphoglycerate mutase deficiency revisitedAli Naini, Antonio Toscano, Olimpia Musumeci, et al.
Neuromuscular Disorders : NMD|March 17, 2009
The m.3244G>A mutation in mtDNA is another cause of progressive external ophthalmoplegiaEvangelia Sotiriou, Jorida Coku, Kurenai Tanji, et al.
Physical Review Letters|June 1, 2004
Multiphoton double ionization via field-independent resonant excitationJ Rudati, J L Chaloupka, P Agostini, et al.
Pageof 95