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M J Bennett

Showing results (241-250 of 351) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1988
Primary hyperoxaluria and L-glyceric aciduria in the catW F Blakemore, M F Heath, M J Bennett, et al.
Neuropediatrics|November 1, 1990
Decreased erythrocyte and platelet phospholipids and fatty acids in juvenile neuronal ceroid-lipofuscinosis (Batten disease)M J Bennett, J H Galloway, I J Cartwright, et al.
The Journal of Pediatrics|March 10, 2001
Molecular prenatal diagnosis in families with fetal mitochondrial trifunctional protein mutationsJ A Ibdah, Y Zhao, J Viola, et al.
Molecular Genetics and Metabolism|March 13, 2001
Placental floor infarction complicating the pregnancy of a fetus with long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiencyD Matern, B M Schehata, P Shekhawa, et al.
European Journal of Clinical Investigation|March 1, 1992
Determinants of fasting plasma triglyceride levels: metabolism of hepatic and intestinal lipoproteinsJ A Cortner, N A Le, P M Coates, et al.
American Journal of Medical Genetics|October 1, 1991
Glutaric aciduria type I: a common cause of episodic encephalopathy and spastic paralysis in the Amish of Lancaster County, PennsylvaniaD H Morton, M J Bennett, L E Seargeant, et al.
British Journal of Anaesthesia|August 21, 2016
Patient factors that influence cerebral desaturation during transcatheter aortic valve implantationM J Bennett, C Brodie, N M Idris, et al.
Bioscience Reports|February 1, 1995
Cholesterol enhances cationic liposome-mediated DNA transfection of human respiratory epithelial cellsM J Bennett, M H Nantz, R P Balasubramaniam, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
Lethal multiple acyl-CoA dehydrogenation deficiency with dysmorphic featuresM J Bennett, R J Pollitt, J M Land, et al.
The Australian & New Zealand Journal of Obstetrics & Gynaecology|February 1, 1986
Chorionic villus sampling. Clinical experience in 50 diagnostic casesD M Wass, P S Warren, L A Stewart, et al.
Pageof 36

Showing results (241-250 of 351) with videos related to

Sort By:
Pageof 36
Journal of Inherited Metabolic Disease|January 1, 1988
Primary hyperoxaluria and L-glyceric aciduria in the catW F Blakemore, M F Heath, M J Bennett, et al.
Neuropediatrics|November 1, 1990
Decreased erythrocyte and platelet phospholipids and fatty acids in juvenile neuronal ceroid-lipofuscinosis (Batten disease)M J Bennett, J H Galloway, I J Cartwright, et al.
The Journal of Pediatrics|March 10, 2001
Molecular prenatal diagnosis in families with fetal mitochondrial trifunctional protein mutationsJ A Ibdah, Y Zhao, J Viola, et al.
Molecular Genetics and Metabolism|March 13, 2001
Placental floor infarction complicating the pregnancy of a fetus with long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiencyD Matern, B M Schehata, P Shekhawa, et al.
European Journal of Clinical Investigation|March 1, 1992
Determinants of fasting plasma triglyceride levels: metabolism of hepatic and intestinal lipoproteinsJ A Cortner, N A Le, P M Coates, et al.
American Journal of Medical Genetics|October 1, 1991
Glutaric aciduria type I: a common cause of episodic encephalopathy and spastic paralysis in the Amish of Lancaster County, PennsylvaniaD H Morton, M J Bennett, L E Seargeant, et al.
British Journal of Anaesthesia|August 21, 2016
Patient factors that influence cerebral desaturation during transcatheter aortic valve implantationM J Bennett, C Brodie, N M Idris, et al.
Bioscience Reports|February 1, 1995
Cholesterol enhances cationic liposome-mediated DNA transfection of human respiratory epithelial cellsM J Bennett, M H Nantz, R P Balasubramaniam, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
Lethal multiple acyl-CoA dehydrogenation deficiency with dysmorphic featuresM J Bennett, R J Pollitt, J M Land, et al.
The Australian & New Zealand Journal of Obstetrics & Gynaecology|February 1, 1986
Chorionic villus sampling. Clinical experience in 50 diagnostic casesD M Wass, P S Warren, L A Stewart, et al.
Pageof 36