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DiMauro

Showing results (671-680 of 942) with videos related to

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The New England Journal of Medicine|May 18, 1989
Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndromeC T Moraes, S DiMauro, M Zeviani, et al.
Acta Neuropathologica|December 10, 2002
The A8344G mutation in mitochondrial DNA associated with stroke-like episodes and gastrointestinal dysfunctionKurenai Tanji, Josep Gamez, Carles Cervera, et al.
Annals of Neurology|June 9, 1999
Exercise intolerance due to a nonsense mutation in the mtDNA ND4 geneA L Andreu, K Tanji, C Bruno, et al.
Science (New York, N.Y.)|August 11, 2000
High-gain harmonic-generation free-electron laserYu, Babzien, Ben-Zvi, et al.
Anales Espanoles De Pediatria|February 1, 1991
[Clinical and biochemical heterogeneity of childhood cytochrome C deficiency. Review of the literature]M Roig Quilis, J Sánchez Esteban, A Lombes, et al.
Plos One|July 24, 2014
Platelet-rich plasma and skeletal muscle healing: a molecular analysis of the early phases of the regeneration process in an experimental animal modelIvan Dimauro, Loredana Grasso, Simona Fittipaldi, et al.
Neurology|February 1, 1991
Differential diagnosis of fatal and benign cytochrome c oxidase-deficient myopathies of infancy: an immunohistochemical approachH J Tritschler, E Bonilla, A Lombes, et al.
Spine|September 11, 2025
Microdose Intrathecal Morphine Injection in Teenagers Undergoing Scoliosis Surgery Decreases Length of Stay, Pain Scores, and Opioid ConsumptionVishal Sarwahi, Alexander Morledge, Anabelle Cohen, et al.
Pediatric Research|November 14, 1997
Deficient muscle carnitine transport in primary carnitine deficiencyR Pons, R Carrozzo, I Tein, et al.
Genetics, Selection, Evolution : GSE|August 14, 2016
Use of canonical discriminant analysis to study signatures of selection in cattleSilvia Sorbolini, Giustino Gaspa, Roberto Steri, et al.
Pageof 95

Showing results (671-680 of 942) with videos related to

Sort By:
Pageof 95
The New England Journal of Medicine|May 18, 1989
Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndromeC T Moraes, S DiMauro, M Zeviani, et al.
Acta Neuropathologica|December 10, 2002
The A8344G mutation in mitochondrial DNA associated with stroke-like episodes and gastrointestinal dysfunctionKurenai Tanji, Josep Gamez, Carles Cervera, et al.
Annals of Neurology|June 9, 1999
Exercise intolerance due to a nonsense mutation in the mtDNA ND4 geneA L Andreu, K Tanji, C Bruno, et al.
Science (New York, N.Y.)|August 11, 2000
High-gain harmonic-generation free-electron laserYu, Babzien, Ben-Zvi, et al.
Anales Espanoles De Pediatria|February 1, 1991
[Clinical and biochemical heterogeneity of childhood cytochrome C deficiency. Review of the literature]M Roig Quilis, J Sánchez Esteban, A Lombes, et al.
Plos One|July 24, 2014
Platelet-rich plasma and skeletal muscle healing: a molecular analysis of the early phases of the regeneration process in an experimental animal modelIvan Dimauro, Loredana Grasso, Simona Fittipaldi, et al.
Neurology|February 1, 1991
Differential diagnosis of fatal and benign cytochrome c oxidase-deficient myopathies of infancy: an immunohistochemical approachH J Tritschler, E Bonilla, A Lombes, et al.
Spine|September 11, 2025
Microdose Intrathecal Morphine Injection in Teenagers Undergoing Scoliosis Surgery Decreases Length of Stay, Pain Scores, and Opioid ConsumptionVishal Sarwahi, Alexander Morledge, Anabelle Cohen, et al.
Pediatric Research|November 14, 1997
Deficient muscle carnitine transport in primary carnitine deficiencyR Pons, R Carrozzo, I Tein, et al.
Genetics, Selection, Evolution : GSE|August 14, 2016
Use of canonical discriminant analysis to study signatures of selection in cattleSilvia Sorbolini, Giustino Gaspa, Roberto Steri, et al.
Pageof 95