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DiMauro

Showing results (661-670 of 942) with videos related to

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JAMA Neurology|November 20, 2013
Branching enzyme deficiency: expanding the clinical spectrumCarmen Paradas, Hasan O Akman, Carolina Ionete, et al.
Medicine and Science in Sports and Exercise|May 1, 2012
Acute exercise modulates BDNF and pro-BDNF protein content in immune cellsAndrea Brunelli, Ivan Dimauro, Paolo Sgrò, et al.
Journal of Inherited Metabolic Disease|May 19, 1998
Primary adrenal insufficiency in a child with a mitochondrial DNA deletionC Bruno, C Minetti, Y Tang, et al.
Child Neurology Open|May 16, 2017
A De Novo Mutation in <i>MTND6</i> Causes Generalized Dystonia in 2 Unrelated ChildrenYasemin Gulcan Kurt, Jorida Çoku, H Orhan Akman, et al.
Neurology|August 1, 1990
Partial dystrophin deficiency in monozygous twin carriers of the Duchenne gene discordant for clinical myopathyE Bonilla, D S Younger, H W Chang, et al.
Muscle & Nerve|October 15, 1998
Study of mitochondrial DNA depletion in muscle by single-fiber polymerase chain reactionM Sciacco, P Gasparo-Rippa, T H Vu, et al.
Journal of the Neurological Sciences|April 1, 1996
Molecular characterization of myophosphorylase deficiency in a group of patients from northern ItalyA Martinuzzi, S Tsujino, L Vergani, et al.
Neurology|July 23, 1998
Molecular genetic analysis of McArdle's disease in Spanish patientsA L Andreu, C Bruno, J Gamez, et al.
Neuromuscular Disorders : NMD|November 2, 1999
Manifesting heterozygotes in a Japanese family with a novel mutation in the muscle-specific phosphoglycerate mutase (PGAM-M) geneG M Hadjigeorgiou, N Kawashima, C Bruno, et al.
Neuromuscular Disorders : NMD|May 1, 1997
Mitochondrial tRNA(Cys) gene mutation (A5814G): a second family with mitochondrial encephalopathyF M Santorelli, G Siciliano, C Casali, et al.
Pageof 95

Showing results (661-670 of 942) with videos related to

Sort By:
Pageof 95
JAMA Neurology|November 20, 2013
Branching enzyme deficiency: expanding the clinical spectrumCarmen Paradas, Hasan O Akman, Carolina Ionete, et al.
Medicine and Science in Sports and Exercise|May 1, 2012
Acute exercise modulates BDNF and pro-BDNF protein content in immune cellsAndrea Brunelli, Ivan Dimauro, Paolo Sgrò, et al.
Journal of Inherited Metabolic Disease|May 19, 1998
Primary adrenal insufficiency in a child with a mitochondrial DNA deletionC Bruno, C Minetti, Y Tang, et al.
Child Neurology Open|May 16, 2017
A De Novo Mutation in <i>MTND6</i> Causes Generalized Dystonia in 2 Unrelated ChildrenYasemin Gulcan Kurt, Jorida Çoku, H Orhan Akman, et al.
Neurology|August 1, 1990
Partial dystrophin deficiency in monozygous twin carriers of the Duchenne gene discordant for clinical myopathyE Bonilla, D S Younger, H W Chang, et al.
Muscle & Nerve|October 15, 1998
Study of mitochondrial DNA depletion in muscle by single-fiber polymerase chain reactionM Sciacco, P Gasparo-Rippa, T H Vu, et al.
Journal of the Neurological Sciences|April 1, 1996
Molecular characterization of myophosphorylase deficiency in a group of patients from northern ItalyA Martinuzzi, S Tsujino, L Vergani, et al.
Neurology|July 23, 1998
Molecular genetic analysis of McArdle's disease in Spanish patientsA L Andreu, C Bruno, J Gamez, et al.
Neuromuscular Disorders : NMD|November 2, 1999
Manifesting heterozygotes in a Japanese family with a novel mutation in the muscle-specific phosphoglycerate mutase (PGAM-M) geneG M Hadjigeorgiou, N Kawashima, C Bruno, et al.
Neuromuscular Disorders : NMD|May 1, 1997
Mitochondrial tRNA(Cys) gene mutation (A5814G): a second family with mitochondrial encephalopathyF M Santorelli, G Siciliano, C Casali, et al.
Pageof 95