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N Gregersen

Showing results (1-10 of 208) with videos related to

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Journal of Inherited Metabolic Disease|June 10, 2006
Protein misfolding disorders: pathogenesis and interventionN Gregersen
Scandinavian Journal of Clinical and Laboratory Investigation. Supplementum|January 1, 1985
The acyl-CoA dehydrogenation deficiencies. Recent advances in the enzymic characterization and understanding of the metabolic and pathophysiological disturbances in patients with acyl-CoA dehydrogenation deficienciesN Gregersen
Journal of Chromatography|March 1, 1979
Specific and sensitive method for the determination of C6--C10 dicarboxylic acids in serum and urine by selected ion monitoringN Gregersen
Journal of Inherited Metabolic Disease|January 1, 1984
Fatty acyl-CoA dehydrogenase deficiency: enzyme measurement and studies on alternative metabolismN Gregersen
Pediatric Research|November 1, 1979
Studies on the effects of saturated and unsaturated short-chain monocarboxylic acids on the energy metabolism of rat liver mitochondriaN Gregersen
Journal of Inherited Metabolic Disease|January 1, 1985
Riboflavin-responsive defects of beta-oxidationN Gregersen
Biochemical Medicine|August 1, 1981
The specific inhibition of the pyruvate dehydrogenase complex from pig kidney by propionyl-CoA and isovaleryl-Co-AN Gregersen
Acta Orthopaedica Scandinavica|January 1, 1974
Malformatio congenita articuli talo-cruralisH N Gregersen
Acta Orthopaedica Scandinavica|January 1, 1971
Fractures of the humerus from muscular violenceH N Gregersen
The Journal of Bone and Joint Surgery. American Volume|January 1, 1977
Naviculocuneiform coalitionH N Gregersen
Pageof 21

Showing results (1-10 of 208) with videos related to

Sort By:
Pageof 21
Journal of Inherited Metabolic Disease|June 10, 2006
Protein misfolding disorders: pathogenesis and interventionN Gregersen
Scandinavian Journal of Clinical and Laboratory Investigation. Supplementum|January 1, 1985
The acyl-CoA dehydrogenation deficiencies. Recent advances in the enzymic characterization and understanding of the metabolic and pathophysiological disturbances in patients with acyl-CoA dehydrogenation deficienciesN Gregersen
Journal of Chromatography|March 1, 1979
Specific and sensitive method for the determination of C6--C10 dicarboxylic acids in serum and urine by selected ion monitoringN Gregersen
Journal of Inherited Metabolic Disease|January 1, 1984
Fatty acyl-CoA dehydrogenase deficiency: enzyme measurement and studies on alternative metabolismN Gregersen
Pediatric Research|November 1, 1979
Studies on the effects of saturated and unsaturated short-chain monocarboxylic acids on the energy metabolism of rat liver mitochondriaN Gregersen
Journal of Inherited Metabolic Disease|January 1, 1985
Riboflavin-responsive defects of beta-oxidationN Gregersen
Biochemical Medicine|August 1, 1981
The specific inhibition of the pyruvate dehydrogenase complex from pig kidney by propionyl-CoA and isovaleryl-Co-AN Gregersen
Acta Orthopaedica Scandinavica|January 1, 1974
Malformatio congenita articuli talo-cruralisH N Gregersen
Acta Orthopaedica Scandinavica|January 1, 1971
Fractures of the humerus from muscular violenceH N Gregersen
The Journal of Bone and Joint Surgery. American Volume|January 1, 1977
Naviculocuneiform coalitionH N Gregersen
Pageof 21