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X Dennett

Showing results (31-40 of 59) with videos related to

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Neurology|September 1, 1987
Mitochondrial studies in Kearns-Sayre syndrome: normal respiratory chain function with absence of a mitochondrial translation productE Byrne, S Marzuki, N Sattayasai, et al.
Journal of Paediatrics and Child Health|April 12, 2000
Elevated aminotransferase as a presenting finding in a patient with occult muscle diseaseT Begum, M R Oliver, A J Kornberg, et al.
The Journal of Rheumatology|May 20, 1999
Incidence of inflammatory myopathies in Victoria, Australia, and evidence of spatial clusteringM Patrick, R Buchbinder, D Jolley, et al.
Biochimica Et Biophysica Acta|November 21, 1991
Mitochondrial genome distribution in histochemically cytochrome c oxidase-negative muscle fibres in patients with a mixture of deleted and wild type mitochondrial DNAS Collins, C Rudduck, S Marzuki, et al.
Journal of Pediatric Orthopedics. Part B|July 1, 1997
Muscle abnormalities in idiopathic toe-walkersD M Eastwood, X Dennett, L K Shield, et al.
Neurology|December 22, 1999
Benign acute childhood myositis: laboratory and clinical featuresM T Mackay, A J Kornberg, L K Shield, et al.
The Journal of Pediatrics|April 1, 1973
Hypertrophic interstitial polyneuropathy in infancy. Clinical and pathologic features in two casesR M Anderson, X Dennett, I J Hopkins, et al.
Australian Paediatric Journal|January 1, 1988
Becker and Duchenne muscular dystrophy: a comparative morphological studyX Dennett, L K Shield, L J Clingan, et al.
The Medical Journal of Australia|December 6, 1993
Emetine myopathy in a patient with an eating disorderD Thyagarajan, B J Day, J Wodak, et al.
Biochemical Medicine and Metabolic Biology|August 1, 1991
Affinity chromatography isolation of human cytochrome oxidase and small-scale Western immunoblot probing of the enzyme complex in mitochondrial cytopathy patientsI Trounce, E Byrne, X Dennett, et al.
Pageof 6

Showing results (31-40 of 59) with videos related to

Sort By:
Pageof 6
Neurology|September 1, 1987
Mitochondrial studies in Kearns-Sayre syndrome: normal respiratory chain function with absence of a mitochondrial translation productE Byrne, S Marzuki, N Sattayasai, et al.
Journal of Paediatrics and Child Health|April 12, 2000
Elevated aminotransferase as a presenting finding in a patient with occult muscle diseaseT Begum, M R Oliver, A J Kornberg, et al.
The Journal of Rheumatology|May 20, 1999
Incidence of inflammatory myopathies in Victoria, Australia, and evidence of spatial clusteringM Patrick, R Buchbinder, D Jolley, et al.
Biochimica Et Biophysica Acta|November 21, 1991
Mitochondrial genome distribution in histochemically cytochrome c oxidase-negative muscle fibres in patients with a mixture of deleted and wild type mitochondrial DNAS Collins, C Rudduck, S Marzuki, et al.
Journal of Pediatric Orthopedics. Part B|July 1, 1997
Muscle abnormalities in idiopathic toe-walkersD M Eastwood, X Dennett, L K Shield, et al.
Neurology|December 22, 1999
Benign acute childhood myositis: laboratory and clinical featuresM T Mackay, A J Kornberg, L K Shield, et al.
The Journal of Pediatrics|April 1, 1973
Hypertrophic interstitial polyneuropathy in infancy. Clinical and pathologic features in two casesR M Anderson, X Dennett, I J Hopkins, et al.
Australian Paediatric Journal|January 1, 1988
Becker and Duchenne muscular dystrophy: a comparative morphological studyX Dennett, L K Shield, L J Clingan, et al.
The Medical Journal of Australia|December 6, 1993
Emetine myopathy in a patient with an eating disorderD Thyagarajan, B J Day, J Wodak, et al.
Biochemical Medicine and Metabolic Biology|August 1, 1991
Affinity chromatography isolation of human cytochrome oxidase and small-scale Western immunoblot probing of the enzyme complex in mitochondrial cytopathy patientsI Trounce, E Byrne, X Dennett, et al.
Pageof 6