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DiMauro

Showing results (311-320 of 942) with videos related to

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Neurology|June 1, 1987
Cardiomyopathy, mental retardation, and autophagic vacuolar myopathyZ H Hart, S Servidei, P L Peterson, et al.
Neurology|April 24, 2002
Exercise-induced muscle "burning," fatigue, and hyper-CKemia: mtDNA T10010C mutation in tRNA(Gly)Y Nishigaki, E Bonilla, S Shanske, et al.
Journal of Experimental and Integrative Medicine|November 23, 2013
A novel <i>POLG</i> gene mutation in a patient with SANDOBulent Kurt, Ali B Naini, William C Copeland, et al.
Annals of Neurology|April 1, 1985
Fatal infantile mitochondrial myopathy and renal dysfunction caused by cytochrome c oxidase deficiency: immunological studies in a new patientM Zeviani, I Nonaka, E Bonilla, et al.
Neurology|June 1, 1985
Physiologic assessment of phosphoglycerate mutase deficiency: incremental exercise testJ T Kissel, W Beam, N Bresolin, et al.
Biochimica Et Biophysica Acta|March 17, 1999
Mitochondrial involvement in Alzheimer's diseaseE Bonilla, K Tanji, M Hirano, et al.
Neurology|May 1, 1996
Multiple mitochondrial DNA deletions associated with autosomal recessive ophthalmoplegia and severe cardiomyopathyS Bohlega, K Tanji, F M Santorelli, et al.
International Journal of Medical Informatics|January 10, 2019
Nasal cytology with deep learning techniquesGiovanni Dimauro, Giorgio Ciprandi, Francesca Deperte, et al.
Neuromuscular Disorders : NMD|January 23, 2009
Myopathic form of phosphoglycerate kinase (PGK) deficiency: a new case and pathogenic considerationsRonen Spiegel, Estela Area Gomez, Hasan O Akman, et al.
Muscle & Nerve|October 8, 2014
A myopathy with unusual features caused by PNPLA2 gene mutationsElena M Pennisi, Sara Missaglia, Salvatore Dimauro, et al.
Pageof 95

Showing results (311-320 of 942) with videos related to

Sort By:
Pageof 95
Neurology|June 1, 1987
Cardiomyopathy, mental retardation, and autophagic vacuolar myopathyZ H Hart, S Servidei, P L Peterson, et al.
Neurology|April 24, 2002
Exercise-induced muscle "burning," fatigue, and hyper-CKemia: mtDNA T10010C mutation in tRNA(Gly)Y Nishigaki, E Bonilla, S Shanske, et al.
Journal of Experimental and Integrative Medicine|November 23, 2013
A novel <i>POLG</i> gene mutation in a patient with SANDOBulent Kurt, Ali B Naini, William C Copeland, et al.
Annals of Neurology|April 1, 1985
Fatal infantile mitochondrial myopathy and renal dysfunction caused by cytochrome c oxidase deficiency: immunological studies in a new patientM Zeviani, I Nonaka, E Bonilla, et al.
Neurology|June 1, 1985
Physiologic assessment of phosphoglycerate mutase deficiency: incremental exercise testJ T Kissel, W Beam, N Bresolin, et al.
Biochimica Et Biophysica Acta|March 17, 1999
Mitochondrial involvement in Alzheimer's diseaseE Bonilla, K Tanji, M Hirano, et al.
Neurology|May 1, 1996
Multiple mitochondrial DNA deletions associated with autosomal recessive ophthalmoplegia and severe cardiomyopathyS Bohlega, K Tanji, F M Santorelli, et al.
International Journal of Medical Informatics|January 10, 2019
Nasal cytology with deep learning techniquesGiovanni Dimauro, Giorgio Ciprandi, Francesca Deperte, et al.
Neuromuscular Disorders : NMD|January 23, 2009
Myopathic form of phosphoglycerate kinase (PGK) deficiency: a new case and pathogenic considerationsRonen Spiegel, Estela Area Gomez, Hasan O Akman, et al.
Muscle & Nerve|October 8, 2014
A myopathy with unusual features caused by PNPLA2 gene mutationsElena M Pennisi, Sara Missaglia, Salvatore Dimauro, et al.
Pageof 95