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DiMauro

Showing results (221-230 of 1,071) with videos related to

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Human Mutation|January 1, 1994
An A-to-C substitution involving the translation initiation codon in a patient with myophosphorylase deficiency (McArdle's disease)S Tsujino, L A Rubin, S Shanske, et al.
BMC Research Notes|September 22, 2012
A simple protocol for the subcellular fractionation of skeletal muscle cells and tissueIvan Dimauro, Timothy Pearson, Daniela Caporossi, et al.
Archives of Neurology|November 10, 2004
A novel polymerase gamma mutation in a family with ophthalmoplegia, neuropathy, and ParkinsonismMichelangelo Mancuso, Massimiliano Filosto, Shin J Oh, et al.
Epilepsy Research. Supplement|January 1, 1991
Epilepsy in mitochondrial encephalomyopathiesS DiMauro, E Ricci, M Hirano, et al.
Behaviour Research and Therapy|December 25, 2012
Long-term effectiveness of CBT for anxiety disorders in an adult outpatient clinic sample: a follow-up studyJennifer DiMauro, Janine Domingues, Geraldine Fernandez, et al.
Sensors (Basel, Switzerland)|June 24, 2022
Industry 4.0 and Precision Livestock Farming (PLF): An up to Date Overview across Animal ProductionsSarah Morrone, Corrado Dimauro, Filippo Gambella, et al.
The Journal of Pediatrics|July 1, 1988
Fatal infantile cardiopathy caused by phosphorylase b kinase deficiencyS Servidei, L A Metlay, J Chodosh, et al.
Neurologic Clinics|February 1, 1989
Mitochondrial diseasesM Zeviani, E Bonilla, D C DeVivo, et al.
Free Radical Biology & Medicine|October 2, 2012
In vitro susceptibility of thioredoxins and glutathione to redox modification and aging-related changes in skeletal muscleIvan Dimauro, Timothy Pearson, Daniela Caporossi, et al.
Journal of Molecular Biology|February 20, 1989
Q beta replicase: mapping the functional domains of an RNA-dependent RNA polymeraseD R Mills, C Priano, P DiMauro, et al.
Pageof 108

Showing results (221-230 of 1,071) with videos related to

Sort By:
Pageof 108
Human Mutation|January 1, 1994
An A-to-C substitution involving the translation initiation codon in a patient with myophosphorylase deficiency (McArdle's disease)S Tsujino, L A Rubin, S Shanske, et al.
BMC Research Notes|September 22, 2012
A simple protocol for the subcellular fractionation of skeletal muscle cells and tissueIvan Dimauro, Timothy Pearson, Daniela Caporossi, et al.
Archives of Neurology|November 10, 2004
A novel polymerase gamma mutation in a family with ophthalmoplegia, neuropathy, and ParkinsonismMichelangelo Mancuso, Massimiliano Filosto, Shin J Oh, et al.
Epilepsy Research. Supplement|January 1, 1991
Epilepsy in mitochondrial encephalomyopathiesS DiMauro, E Ricci, M Hirano, et al.
Behaviour Research and Therapy|December 25, 2012
Long-term effectiveness of CBT for anxiety disorders in an adult outpatient clinic sample: a follow-up studyJennifer DiMauro, Janine Domingues, Geraldine Fernandez, et al.
Sensors (Basel, Switzerland)|June 24, 2022
Industry 4.0 and Precision Livestock Farming (PLF): An up to Date Overview across Animal ProductionsSarah Morrone, Corrado Dimauro, Filippo Gambella, et al.
The Journal of Pediatrics|July 1, 1988
Fatal infantile cardiopathy caused by phosphorylase b kinase deficiencyS Servidei, L A Metlay, J Chodosh, et al.
Neurologic Clinics|February 1, 1989
Mitochondrial diseasesM Zeviani, E Bonilla, D C DeVivo, et al.
Free Radical Biology & Medicine|October 2, 2012
In vitro susceptibility of thioredoxins and glutathione to redox modification and aging-related changes in skeletal muscleIvan Dimauro, Timothy Pearson, Daniela Caporossi, et al.
Journal of Molecular Biology|February 20, 1989
Q beta replicase: mapping the functional domains of an RNA-dependent RNA polymeraseD R Mills, C Priano, P DiMauro, et al.
Pageof 108