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S Shanske

Showing results (111-120 of 141) with videos related to

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Neurology|July 23, 1998
Molecular genetic analysis of McArdle's disease in Spanish patientsA L Andreu, C Bruno, J Gamez, et al.
Neurology|November 18, 1998
Missense mutation in the mtDNA cytochrome b gene in a patient with myopathyA L Andreu, C Bruno, S Shanske, et al.
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.
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.
Journal of the Neurological Sciences|July 13, 1999
A new mitochondrial DNA mutation (A3288G) in the tRNA(Leu(UUR)) gene associated with familial myopathyG M Hadjigeorgiou, S H Kim, K H Fischbeck, et al.
Revue Neurologique|January 1, 1991
Mitochondrial encephalomyopathies: biochemical approachS Dimauro, C T Moraes, S Shanske, et al.
Fetal Diagnosis and Therapy|March 27, 2009
Intracerebral periventricular pseudocysts in a fetus with mitochondrial depletion syndrome: an association or coincidenceM Rohrbach, D Chitayat, G Maegawa, et al.
Journal of Child Neurology|July 17, 2001
A5814G mutation in mitochondrial DNA can cause mitochondrial myopathy and cardiomyopathyC Karadimas, K Tanji, M Geremek, et al.
Neuromuscular Disorders : NMD|November 2, 1999
A novel missense mutation in the glycogen branching enzyme gene in a child with myopathy and hepatopathyC Bruno, M DiRocco, L D Lamba, et al.
Neurology|April 28, 2004
Cerebral lactic acidosis correlates with neurological impairment in MELASP Kaufmann, D C Shungu, M C Sano, et al.
Pageof 15

Showing results (111-120 of 141) with videos related to

Sort By:
Pageof 15
Neurology|July 23, 1998
Molecular genetic analysis of McArdle's disease in Spanish patientsA L Andreu, C Bruno, J Gamez, et al.
Neurology|November 18, 1998
Missense mutation in the mtDNA cytochrome b gene in a patient with myopathyA L Andreu, C Bruno, S Shanske, et al.
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.
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.
Journal of the Neurological Sciences|July 13, 1999
A new mitochondrial DNA mutation (A3288G) in the tRNA(Leu(UUR)) gene associated with familial myopathyG M Hadjigeorgiou, S H Kim, K H Fischbeck, et al.
Revue Neurologique|January 1, 1991
Mitochondrial encephalomyopathies: biochemical approachS Dimauro, C T Moraes, S Shanske, et al.
Fetal Diagnosis and Therapy|March 27, 2009
Intracerebral periventricular pseudocysts in a fetus with mitochondrial depletion syndrome: an association or coincidenceM Rohrbach, D Chitayat, G Maegawa, et al.
Journal of Child Neurology|July 17, 2001
A5814G mutation in mitochondrial DNA can cause mitochondrial myopathy and cardiomyopathyC Karadimas, K Tanji, M Geremek, et al.
Neuromuscular Disorders : NMD|November 2, 1999
A novel missense mutation in the glycogen branching enzyme gene in a child with myopathy and hepatopathyC Bruno, M DiRocco, L D Lamba, et al.
Neurology|April 28, 2004
Cerebral lactic acidosis correlates with neurological impairment in MELASP Kaufmann, D C Shungu, M C Sano, et al.
Pageof 15