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M J Bennett

Showing results (171-180 of 351) with videos related to

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The Journal of Pediatrics|January 1, 1995
Transient organic aciduria and persistent lacticacidemia in a patient with short-chain acyl-coenzyme A dehydrogenase deficiencyD B Dawson, L Waber, D E Hale, et al.
The Journal of Pediatrics|April 17, 1998
3-Methylcrotonyl-coenzyme A carboxylase deficiency in Amish/Mennonite adults identified by detection of increased acylcarnitines in blood spots of their childrenK M Gibson, M J Bennett, E W Naylor, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Late-onset holocarboxylase synthetase deficiencyK M Gibson, M J Bennett, W L Nyhan, et al.
The American Journal of Forensic Medicine and Pathology|December 1, 1996
Comment on "Whole blood levels of dodecanoic acid, a routinely detectable forensic marker for a genetic disease often misdiagnosed as sudden infant death syndrome (SIDS): MCAD deficiency"K F Ross, J M Guileyardo, M J Bennett, et al.
Bulletin of Mathematical Biology|February 6, 2010
Mathematical modelling of the Aux/IAA negative feedback loopA M Middleton, J R King, M J Bennett, et al.
Biology of the Neonate|January 1, 1977
The development of glycolytic and pentose phosphate shunt enzymes in human brainM J Bennett, W R Timperley, C B Taylor, et al.
Lipids|August 15, 2000
Gastroprotection of DNA with a synthetic cholic acid analogE J Niedzinski, M J Bennett, D C Olson, et al.
Molecular Genetics and Metabolism|September 26, 2000
Synergistic heterozygosity: disease resulting from multiple partial defects in one or more metabolic pathwaysJ Vockley, P Rinaldo, M J Bennett, et al.
Molecular Genetics and Metabolism|July 20, 2001
Impaired mitochondrial fatty acid oxidative flux in fibroblasts from a patient with malonyl-CoA decarboxylase deficiencyM J Bennett, P A Harthcock, R L Boriack, et al.
American Journal of Medical Genetics|August 1, 1994
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase (L-CHAD) deficiency in a patient with the Bannayan-Riley-Ruvalcaba syndromeJ S Fryburg, J P Pelegano, M J Bennett, et al.
Pageof 36

Showing results (171-180 of 351) with videos related to

Sort By:
Pageof 36
The Journal of Pediatrics|January 1, 1995
Transient organic aciduria and persistent lacticacidemia in a patient with short-chain acyl-coenzyme A dehydrogenase deficiencyD B Dawson, L Waber, D E Hale, et al.
The Journal of Pediatrics|April 17, 1998
3-Methylcrotonyl-coenzyme A carboxylase deficiency in Amish/Mennonite adults identified by detection of increased acylcarnitines in blood spots of their childrenK M Gibson, M J Bennett, E W Naylor, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Late-onset holocarboxylase synthetase deficiencyK M Gibson, M J Bennett, W L Nyhan, et al.
The American Journal of Forensic Medicine and Pathology|December 1, 1996
Comment on "Whole blood levels of dodecanoic acid, a routinely detectable forensic marker for a genetic disease often misdiagnosed as sudden infant death syndrome (SIDS): MCAD deficiency"K F Ross, J M Guileyardo, M J Bennett, et al.
Bulletin of Mathematical Biology|February 6, 2010
Mathematical modelling of the Aux/IAA negative feedback loopA M Middleton, J R King, M J Bennett, et al.
Biology of the Neonate|January 1, 1977
The development of glycolytic and pentose phosphate shunt enzymes in human brainM J Bennett, W R Timperley, C B Taylor, et al.
Lipids|August 15, 2000
Gastroprotection of DNA with a synthetic cholic acid analogE J Niedzinski, M J Bennett, D C Olson, et al.
Molecular Genetics and Metabolism|September 26, 2000
Synergistic heterozygosity: disease resulting from multiple partial defects in one or more metabolic pathwaysJ Vockley, P Rinaldo, M J Bennett, et al.
Molecular Genetics and Metabolism|July 20, 2001
Impaired mitochondrial fatty acid oxidative flux in fibroblasts from a patient with malonyl-CoA decarboxylase deficiencyM J Bennett, P A Harthcock, R L Boriack, et al.
American Journal of Medical Genetics|August 1, 1994
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase (L-CHAD) deficiency in a patient with the Bannayan-Riley-Ruvalcaba syndromeJ S Fryburg, J P Pelegano, M J Bennett, et al.
Pageof 36