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DiMauro

Showing results (751-760 of 942) with videos related to

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Archives of Neurology|February 19, 2000
A novel missense mutation (W797R) in the myophosphorylase gene in Spanish patients with McArdle diseaseR Fernández, C Navarro, A L Andreu, et al.
Neurology|April 12, 2003
Reversion of mtDNA depletion in a patient with TK2 deficiencyM R Vilà, T Segovia-Silvestre, J Gámez, et al.
Neuromuscular Disorders : NMD|July 19, 2003
A novel mitochondrial tRNA(Leu(UUR)) mutation in a patient with features of MERRF and Kearns-Sayre syndromeYutaka Nishigaki, Saba Tadesse, Eduardo Bonilla, et al.
The Biochemical Journal|August 25, 2004
Biochemical analysis of respiratory function in cybrid cell lines harbouring mitochondrial DNA mutationsFrancesco Pallotti, Alessandra Baracca, Evelyn Hernandez-Rosa, et al.
Archives of Osteoporosis|December 27, 2024
Effects of 12-week power training on bone in mobility-limited older adults: randomised controlled trialValentina Muollo, Lars G Hvid, Vikram V Shanbhogue, et al.
Neurobiology of Disease|January 22, 2013
Mitochondrial abnormalities in temporal lobe of autistic brainGuomei Tang, Puri Gutierrez Rios, Sheng-Han Kuo, et al.
Antioxidants (Basel, Switzerland)|August 29, 2020
The Phosphodiesterase Type 5 Inhibitor Sildenafil Improves DNA Stability and Redox Homeostasis in Systemic Sclerosis Fibroblasts Exposed to Reactive Oxygen SpeciesLuigi Di Luigi, Guglielmo Duranti, Ambra Antonioni, et al.
Journal of Inherited Metabolic Disease|November 3, 2020
GBE1-related disorders: Adult polyglucosan body disease and its neuromuscular phenotypesPaulo Victor Sgobbi Souza, Bruno Mattos Lombardi Badia, Igor Braga Farias, et al.
Physical Review Letters|April 16, 2021
Molecular Modes of Attosecond Charge MigrationAderonke S Folorunso, Adam Bruner, François Mauger, et al.
Neurology|September 12, 2000
Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNAC L Karadimas, P Greenstein, C M Sue, et al.
Pageof 95

Showing results (751-760 of 942) with videos related to

Sort By:
Pageof 95
Archives of Neurology|February 19, 2000
A novel missense mutation (W797R) in the myophosphorylase gene in Spanish patients with McArdle diseaseR Fernández, C Navarro, A L Andreu, et al.
Neurology|April 12, 2003
Reversion of mtDNA depletion in a patient with TK2 deficiencyM R Vilà, T Segovia-Silvestre, J Gámez, et al.
Neuromuscular Disorders : NMD|July 19, 2003
A novel mitochondrial tRNA(Leu(UUR)) mutation in a patient with features of MERRF and Kearns-Sayre syndromeYutaka Nishigaki, Saba Tadesse, Eduardo Bonilla, et al.
The Biochemical Journal|August 25, 2004
Biochemical analysis of respiratory function in cybrid cell lines harbouring mitochondrial DNA mutationsFrancesco Pallotti, Alessandra Baracca, Evelyn Hernandez-Rosa, et al.
Archives of Osteoporosis|December 27, 2024
Effects of 12-week power training on bone in mobility-limited older adults: randomised controlled trialValentina Muollo, Lars G Hvid, Vikram V Shanbhogue, et al.
Neurobiology of Disease|January 22, 2013
Mitochondrial abnormalities in temporal lobe of autistic brainGuomei Tang, Puri Gutierrez Rios, Sheng-Han Kuo, et al.
Antioxidants (Basel, Switzerland)|August 29, 2020
The Phosphodiesterase Type 5 Inhibitor Sildenafil Improves DNA Stability and Redox Homeostasis in Systemic Sclerosis Fibroblasts Exposed to Reactive Oxygen SpeciesLuigi Di Luigi, Guglielmo Duranti, Ambra Antonioni, et al.
Journal of Inherited Metabolic Disease|November 3, 2020
GBE1-related disorders: Adult polyglucosan body disease and its neuromuscular phenotypesPaulo Victor Sgobbi Souza, Bruno Mattos Lombardi Badia, Igor Braga Farias, et al.
Physical Review Letters|April 16, 2021
Molecular Modes of Attosecond Charge MigrationAderonke S Folorunso, Adam Bruner, François Mauger, et al.
Neurology|September 12, 2000
Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNAC L Karadimas, P Greenstein, C M Sue, et al.
Pageof 95