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D J Hayes

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Electroencephalography and Clinical Neurophysiology. Supplement|January 1, 1987
The mitochondrial myopathies. Defects of the mitochondrial respiratory chain and oxidative phosphorylation systemJ A Morgan-Hughes, J M Cooper, A H Schapira, et al.
Australian Paediatric Journal|January 1, 1988
Human mitochondrial respiratory chain deficienciesJ A Morgan-Hughes, A H Schapira, J M Cooper, et al.
Brain : a Journal of Neurology|August 1, 1992
Treatment of experimental NADH ubiquinone reductase deficiency with menadioneJ M Cooper, D J Hayes, R A Challiss, et al.
Journal of the Neurological Sciences|November 1, 1985
A mitochondrial encephalomyopathy. A combined 31P magnetic resonance and biochemical investigationD J Hayes, D Hilton-Jones, D L Arnold, et al.
Molecular and Biochemical Parasitology|January 15, 1990
The effect of two novel analogues of antimycin A on oxygen consumption and survival of filarial nematodes in vitroD J Hayes, A B O'Dowd, D L Selwood, et al.
Bulletin of Environmental Contamination and Toxicology|January 1, 1983
Comparative acute oral toxicity of para-aminopropiophenone (PAPP) in mammals and birdsP J Savarie, H P Pan, D J Hayes, et al.
Brain : a Journal of Neurology|September 1, 1982
Mitochondrial encephalomyopathies: biochemical studies in two cases revealing defects in the respiratory chainJ A Morgan-Hughes, D J Hayes, J B Clark, et al.
Surgical Endoscopy|December 30, 2004
Development and transferability of a cost-effective laparoscopic camera navigation simulatorJ R Korndorffer, D J Hayes, J B Dunne, et al.
Journal of the Neurological Sciences|December 1, 1987
An unusual metabolic myopathy: a malate-aspartate shuttle defectD J Hayes, D J Taylor, P J Bore, et al.
Journal of the Neurological Sciences|February 1, 1988
An animal model of mitochondrial myopathy: a biochemical and physiological investigation of rats treated in vivo with the NADH-CoQ reductase inhibitor, diphenyleneiodoniumJ M Cooper, R K Petty, D J Hayes, et al.
Pageof 6

Showing results (41-50 of 52) with videos related to

Sort By:
Pageof 6
Electroencephalography and Clinical Neurophysiology. Supplement|January 1, 1987
The mitochondrial myopathies. Defects of the mitochondrial respiratory chain and oxidative phosphorylation systemJ A Morgan-Hughes, J M Cooper, A H Schapira, et al.
Australian Paediatric Journal|January 1, 1988
Human mitochondrial respiratory chain deficienciesJ A Morgan-Hughes, A H Schapira, J M Cooper, et al.
Brain : a Journal of Neurology|August 1, 1992
Treatment of experimental NADH ubiquinone reductase deficiency with menadioneJ M Cooper, D J Hayes, R A Challiss, et al.
Journal of the Neurological Sciences|November 1, 1985
A mitochondrial encephalomyopathy. A combined 31P magnetic resonance and biochemical investigationD J Hayes, D Hilton-Jones, D L Arnold, et al.
Molecular and Biochemical Parasitology|January 15, 1990
The effect of two novel analogues of antimycin A on oxygen consumption and survival of filarial nematodes in vitroD J Hayes, A B O'Dowd, D L Selwood, et al.
Bulletin of Environmental Contamination and Toxicology|January 1, 1983
Comparative acute oral toxicity of para-aminopropiophenone (PAPP) in mammals and birdsP J Savarie, H P Pan, D J Hayes, et al.
Brain : a Journal of Neurology|September 1, 1982
Mitochondrial encephalomyopathies: biochemical studies in two cases revealing defects in the respiratory chainJ A Morgan-Hughes, D J Hayes, J B Clark, et al.
Surgical Endoscopy|December 30, 2004
Development and transferability of a cost-effective laparoscopic camera navigation simulatorJ R Korndorffer, D J Hayes, J B Dunne, et al.
Journal of the Neurological Sciences|December 1, 1987
An unusual metabolic myopathy: a malate-aspartate shuttle defectD J Hayes, D J Taylor, P J Bore, et al.
Journal of the Neurological Sciences|February 1, 1988
An animal model of mitochondrial myopathy: a biochemical and physiological investigation of rats treated in vivo with the NADH-CoQ reductase inhibitor, diphenyleneiodoniumJ M Cooper, R K Petty, D J Hayes, et al.
Pageof 6