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N Gregersen

Showing results (11-20 of 208) with videos related to

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Nordisk Medicin|November 25, 1971
[Malformation congenita art. talo-cruralis]H N Gregersen
Acta Paediatrica Scandinavica|September 1, 1979
The excretion of C6-C10-dicarboxylic acids in the urine of newborn infants during starvation. Evidence for omega-oxidation of fatty acids in the newbornN Gregersen, J Ingerslev
Biochemical Medicine and Metabolic Biology|August 1, 1986
Acyl-CoA:glycine N-acyltransferase: organelle localization and affinity toward straight- and branched-chained acyl-CoA esters in rat liverS Kølvraa, N Gregersen
Journal of Inherited Metabolic Disease|January 1, 1984
Medium chain acyl-CoA dehydrogenase deficiency: apparent Km and Vmax values for fibroblast acyl-CoA dehydrogenase towards octanoyl CoA in patient and control cell linesN Gregersen, S Kølvraa
Biochimica Et Biophysica Acta|May 21, 1986
In vitro studies on the oxidation of medium-chain dicarboxylic acids in rat liverS Kølvraa, N Gregersen
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 11, 1980
Medium-chain triglyceride medication as a pitfall in the diagnosis of non-ketotic C6-C10-dicarboxylic aciduriasP B Mortensen, N Gregersen
Biochimica Et Biophysica Acta|March 12, 1982
The biological origin of ketotic dicarboxylic aciduria. II. In vivo and in vitro investigations of the beta-oxidation of C8-C16-dicarboxylic acids in unstarved, starved and diabetic ratsP B Mortensen, N Gregersen
Scandinavian Journal of Plastic and Reconstructive Surgery|January 1, 1986
Giant incisional hernias closed with polypropylene meshH Kjeldsen, B N Gregersen
Biochimica Et Biophysica Acta|December 23, 1981
The biological origin of ketotic dicarboxylic aciduria. In vivo and in vitro investigations of the omega-oxidation of C6-C16-monocarboxylic acids in unstarved, starved and diabetic ratsP B Mortensen, N Gregersen
Pediatric Research|September 1, 1979
Ketotic episodes in glutaryl-CoA dehydrogenase deficiency (glutaric aciduria)N Gregersen, N J Brandt
Pageof 21

Showing results (11-20 of 208) with videos related to

Sort By:
Pageof 21
Nordisk Medicin|November 25, 1971
[Malformation congenita art. talo-cruralis]H N Gregersen
Acta Paediatrica Scandinavica|September 1, 1979
The excretion of C6-C10-dicarboxylic acids in the urine of newborn infants during starvation. Evidence for omega-oxidation of fatty acids in the newbornN Gregersen, J Ingerslev
Biochemical Medicine and Metabolic Biology|August 1, 1986
Acyl-CoA:glycine N-acyltransferase: organelle localization and affinity toward straight- and branched-chained acyl-CoA esters in rat liverS Kølvraa, N Gregersen
Journal of Inherited Metabolic Disease|January 1, 1984
Medium chain acyl-CoA dehydrogenase deficiency: apparent Km and Vmax values for fibroblast acyl-CoA dehydrogenase towards octanoyl CoA in patient and control cell linesN Gregersen, S Kølvraa
Biochimica Et Biophysica Acta|May 21, 1986
In vitro studies on the oxidation of medium-chain dicarboxylic acids in rat liverS Kølvraa, N Gregersen
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 11, 1980
Medium-chain triglyceride medication as a pitfall in the diagnosis of non-ketotic C6-C10-dicarboxylic aciduriasP B Mortensen, N Gregersen
Biochimica Et Biophysica Acta|March 12, 1982
The biological origin of ketotic dicarboxylic aciduria. II. In vivo and in vitro investigations of the beta-oxidation of C8-C16-dicarboxylic acids in unstarved, starved and diabetic ratsP B Mortensen, N Gregersen
Scandinavian Journal of Plastic and Reconstructive Surgery|January 1, 1986
Giant incisional hernias closed with polypropylene meshH Kjeldsen, B N Gregersen
Biochimica Et Biophysica Acta|December 23, 1981
The biological origin of ketotic dicarboxylic aciduria. In vivo and in vitro investigations of the omega-oxidation of C6-C16-monocarboxylic acids in unstarved, starved and diabetic ratsP B Mortensen, N Gregersen
Pediatric Research|September 1, 1979
Ketotic episodes in glutaryl-CoA dehydrogenase deficiency (glutaric aciduria)N Gregersen, N J Brandt
Pageof 21