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C T Moraes

Showing results (61-70 of 88) with videos related to

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Gut|October 24, 2007
Pathophysiology and fate of hepatocytes in a mouse model of mitochondrial hepatopathiesF Diaz, S Garcia, D Hernandez, et al.
Neurology|September 1, 1988
Deletions of mitochondrial DNA in Kearns-Sayre syndromeM Zeviani, C T Moraes, S DiMauro, et al.
Neurology|December 17, 1998
Deletions of mitochondrial DNA in Kearns-Sayre syndrome. 1988M Zeviani, C T Moraes, S DiMauro, et al.
The Journal of Clinical Endocrinology and Metabolism|January 22, 1998
Mitochondrial encephalomyopathy and hypoparathyroidism associated with a duplication and a deletion of mitochondrial deoxyribonucleic acidC H Tengan, B H Kiyomoto, M S Rocha, et al.
Neuromuscular Disorders : NMD|September 1, 1995
A new mutation associated with MELAS is located in a mitochondrial DNA polypeptide-coding geneG Manfredi, E A Schon, C T Moraes, et al.
Annals of the New York Academy of Sciences|January 1, 1988
Clinical and biochemical studies on cytochrome oxidase deficienciesE A Schon, E Bonilla, A Lombes, et al.
Progress in Clinical and Biological Research|January 1, 1989
Mitochondrial encephalomyopathiesS DiMauro, M Zeviani, C T Moraes, et al.
Research Publications - Association for Research in Nervous and Mental Disease|January 1, 1993
Mitochondrial dysfunction as a mechanism of CNS injuryS DiMauro, S Simonetti, X Chen, et al.
Muscle & Nerve. Supplement|January 1, 1995
Phenotype-genotype correlations in skeletal muscle of patients with mtDNA deletionsC T Moraes, M Sciacco, E Ricci, et al.
Cardiovascular Research|March 23, 2000
Mitochondrial function in heart muscle from patients with idiopathic dilated cardiomyopathyD Jarreta, J Orús, A Barrientos, et al.
Pageof 9

Showing results (61-70 of 88) with videos related to

Sort By:
Pageof 9
Gut|October 24, 2007
Pathophysiology and fate of hepatocytes in a mouse model of mitochondrial hepatopathiesF Diaz, S Garcia, D Hernandez, et al.
Neurology|September 1, 1988
Deletions of mitochondrial DNA in Kearns-Sayre syndromeM Zeviani, C T Moraes, S DiMauro, et al.
Neurology|December 17, 1998
Deletions of mitochondrial DNA in Kearns-Sayre syndrome. 1988M Zeviani, C T Moraes, S DiMauro, et al.
The Journal of Clinical Endocrinology and Metabolism|January 22, 1998
Mitochondrial encephalomyopathy and hypoparathyroidism associated with a duplication and a deletion of mitochondrial deoxyribonucleic acidC H Tengan, B H Kiyomoto, M S Rocha, et al.
Neuromuscular Disorders : NMD|September 1, 1995
A new mutation associated with MELAS is located in a mitochondrial DNA polypeptide-coding geneG Manfredi, E A Schon, C T Moraes, et al.
Annals of the New York Academy of Sciences|January 1, 1988
Clinical and biochemical studies on cytochrome oxidase deficienciesE A Schon, E Bonilla, A Lombes, et al.
Progress in Clinical and Biological Research|January 1, 1989
Mitochondrial encephalomyopathiesS DiMauro, M Zeviani, C T Moraes, et al.
Research Publications - Association for Research in Nervous and Mental Disease|January 1, 1993
Mitochondrial dysfunction as a mechanism of CNS injuryS DiMauro, S Simonetti, X Chen, et al.
Muscle & Nerve. Supplement|January 1, 1995
Phenotype-genotype correlations in skeletal muscle of patients with mtDNA deletionsC T Moraes, M Sciacco, E Ricci, et al.
Cardiovascular Research|March 23, 2000
Mitochondrial function in heart muscle from patients with idiopathic dilated cardiomyopathyD Jarreta, J Orús, A Barrientos, et al.
Pageof 9