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DiMauro

Showing results (641-650 of 942) with videos related to

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Spine|May 19, 2025
Posterior Spinal Fusion with Rib Resection Allows for Improved Deformity Correction as well as Patient SatisfactionVishal Sarwahi, Katherine Eigo, Effat Rahman, et al.
Annals of Neurology|December 16, 1998
The mitochondrial DNA A8344G mutation in Leigh syndrome revealed by analysis in paraffin-embedded sections: revisiting the pastF M Santorelli, K Tanji, S Shanske, et al.
The Journal of Biological Chemistry|June 25, 1989
A gene specifying subunit VIII of human cytochrome c oxidase is localized to chromosome 11 and is expressed in both muscle and non-muscle tissuesR Rizzuto, H Nakase, B Darras, et al.
Mechanisms of Ageing and Development|November 26, 2019
Endurance training improves plasma superoxide dismutase activity in healthy elderlyRoberta Ceci, Guglielmo Duranti, Ester Sara Di Filippo, et al.
The Journal of Pediatrics|July 1, 1987
Severe cardiopathy in branching enzyme deficiencyS Servidei, R E Riepe, C Langston, et al.
Neurology|July 11, 2001
Myopathy with tubulin-reactive crystalline inclusionsT H Vu, A P Hays, K Tanji, et al.
Neuromuscular Disorders : NMD|December 15, 2015
Late-onset polyglucosan body myopathy in five patients with a homozygous mutation in GYG1H Orhan Akman, Yavuz Aykit, Ozge Ceren Amuk, et al.
The American Journal of Pathology|January 4, 2007
Caveolin-1(-/-)- and caveolin-2(-/-)-deficient mice both display numerous skeletal muscle abnormalities, with tubular aggregate formationWilliam Schubert, Federica Sotgia, Alex W Cohen, et al.
Acta Neuropathologica|January 1, 1987
Myo-, neuro-, gastrointestinal encephalopathy (MNGIE syndrome) due to partial deficiency of cytochrome-c-oxidase. A new mitochondrial multisystem disorderA Bardosi, W Creutzfeldt, S DiMauro, et al.
Arquivos De Neuro-Psiquiatria|March 1, 1990
Mitochondrial myopathy and myoclonic epilepsyW O Arruda, L F Torres, A Lombes, et al.
Pageof 95

Showing results (641-650 of 942) with videos related to

Sort By:
Pageof 95
Spine|May 19, 2025
Posterior Spinal Fusion with Rib Resection Allows for Improved Deformity Correction as well as Patient SatisfactionVishal Sarwahi, Katherine Eigo, Effat Rahman, et al.
Annals of Neurology|December 16, 1998
The mitochondrial DNA A8344G mutation in Leigh syndrome revealed by analysis in paraffin-embedded sections: revisiting the pastF M Santorelli, K Tanji, S Shanske, et al.
The Journal of Biological Chemistry|June 25, 1989
A gene specifying subunit VIII of human cytochrome c oxidase is localized to chromosome 11 and is expressed in both muscle and non-muscle tissuesR Rizzuto, H Nakase, B Darras, et al.
Mechanisms of Ageing and Development|November 26, 2019
Endurance training improves plasma superoxide dismutase activity in healthy elderlyRoberta Ceci, Guglielmo Duranti, Ester Sara Di Filippo, et al.
The Journal of Pediatrics|July 1, 1987
Severe cardiopathy in branching enzyme deficiencyS Servidei, R E Riepe, C Langston, et al.
Neurology|July 11, 2001
Myopathy with tubulin-reactive crystalline inclusionsT H Vu, A P Hays, K Tanji, et al.
Neuromuscular Disorders : NMD|December 15, 2015
Late-onset polyglucosan body myopathy in five patients with a homozygous mutation in GYG1H Orhan Akman, Yavuz Aykit, Ozge Ceren Amuk, et al.
The American Journal of Pathology|January 4, 2007
Caveolin-1(-/-)- and caveolin-2(-/-)-deficient mice both display numerous skeletal muscle abnormalities, with tubular aggregate formationWilliam Schubert, Federica Sotgia, Alex W Cohen, et al.
Acta Neuropathologica|January 1, 1987
Myo-, neuro-, gastrointestinal encephalopathy (MNGIE syndrome) due to partial deficiency of cytochrome-c-oxidase. A new mitochondrial multisystem disorderA Bardosi, W Creutzfeldt, S DiMauro, et al.
Arquivos De Neuro-Psiquiatria|March 1, 1990
Mitochondrial myopathy and myoclonic epilepsyW O Arruda, L F Torres, A Lombes, et al.
Pageof 95