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Michael J Bennett

Showing results (21-30 of 156) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|January 16, 2010
Urine organic acid analysis for inherited metabolic disease using gas chromatography-mass spectrometryPatricia M Jones, Michael J Bennett
Molecular Genetics and Metabolism|November 4, 2008
Short-chain acyl-coenzyme A dehydrogenase deficiencyReena Jethva, Michael J Bennett, Jerry Vockley
Methods in Cell Biology|March 19, 2020
Biochemical assays of TCA cycle and β-oxidation metabolitesMichael J Bennett, Feng Sheng, Ann Saada
Annual Review of Physiology|February 5, 2002
Fatty acid oxidation disordersPiero Rinaldo, Dietrich Matern, Michael J Bennett
Laboratory Investigation; a Journal of Technical Methods and Pathology|July 16, 2002
Long-chain L-3-hydroxyacyl-coenzyme a dehydrogenase deficiency: a molecular and biochemical reviewDinesh Rakheja, Michael J Bennett, Beverly B Rogers
Molecular Genetics and Metabolism|October 27, 2007
Intermediate levels of neuronal palmitoyl-protein Delta-9 desaturase in heterozygotes for murine Batten diseaseSrinivas B Narayan, Lu Tan, Michael J Bennett
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|January 24, 2024
Establishing consensus recommendations for long-term osteoporosis care for patients who have attended an Australian fracture liaison service: a Delphi studyMichael J Bennett, Jacqueline R Center, Lin Perry
Current Molecular Medicine|September 28, 2007
Juvenile neuronal ceroid-lipofuscinosis (Batten disease): a brief review and updateDinesh Rakheja, Srinivas B Narayan, Michael J Bennett
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|June 25, 2024
Author response to an editorialMichael J Bennett, Jacqueline R Center, Lin Perry
Pediatric Research|March 7, 2003
Accumulation of 3-hydroxy-fatty acids in the culture medium of long-chain L-3-hydroxyacyl CoA dehydrogenase (LCHAD) and mitochondrial trifunctional protein-deficient skin fibroblasts: implications for medium chain triglyceride dietary treatment of LCHAD deficiencyPatricia M Jones, Yasmeen Butt, Michael J Bennett
Pageof 16

Showing results (21-30 of 156) with videos related to

Sort By:
Pageof 16
Methods in Molecular Biology (Clifton, N.J.)|January 16, 2010
Urine organic acid analysis for inherited metabolic disease using gas chromatography-mass spectrometryPatricia M Jones, Michael J Bennett
Molecular Genetics and Metabolism|November 4, 2008
Short-chain acyl-coenzyme A dehydrogenase deficiencyReena Jethva, Michael J Bennett, Jerry Vockley
Methods in Cell Biology|March 19, 2020
Biochemical assays of TCA cycle and β-oxidation metabolitesMichael J Bennett, Feng Sheng, Ann Saada
Annual Review of Physiology|February 5, 2002
Fatty acid oxidation disordersPiero Rinaldo, Dietrich Matern, Michael J Bennett
Laboratory Investigation; a Journal of Technical Methods and Pathology|July 16, 2002
Long-chain L-3-hydroxyacyl-coenzyme a dehydrogenase deficiency: a molecular and biochemical reviewDinesh Rakheja, Michael J Bennett, Beverly B Rogers
Molecular Genetics and Metabolism|October 27, 2007
Intermediate levels of neuronal palmitoyl-protein Delta-9 desaturase in heterozygotes for murine Batten diseaseSrinivas B Narayan, Lu Tan, Michael J Bennett
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|January 24, 2024
Establishing consensus recommendations for long-term osteoporosis care for patients who have attended an Australian fracture liaison service: a Delphi studyMichael J Bennett, Jacqueline R Center, Lin Perry
Current Molecular Medicine|September 28, 2007
Juvenile neuronal ceroid-lipofuscinosis (Batten disease): a brief review and updateDinesh Rakheja, Srinivas B Narayan, Michael J Bennett
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|June 25, 2024
Author response to an editorialMichael J Bennett, Jacqueline R Center, Lin Perry
Pediatric Research|March 7, 2003
Accumulation of 3-hydroxy-fatty acids in the culture medium of long-chain L-3-hydroxyacyl CoA dehydrogenase (LCHAD) and mitochondrial trifunctional protein-deficient skin fibroblasts: implications for medium chain triglyceride dietary treatment of LCHAD deficiencyPatricia M Jones, Yasmeen Butt, Michael J Bennett
Pageof 16