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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 newborn
N 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 liver
S 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 lines
N Gregersen, S Kølvraa
Biochimica Et Biophysica Acta
|
May 21, 1986
In vitro studies on the oxidation of medium-chain dicarboxylic acids in rat liver
S 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 acidurias
P 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 rats
P B Mortensen, N Gregersen
Scandinavian Journal of Plastic and Reconstructive Surgery
|
January 1, 1986
Giant incisional hernias closed with polypropylene mesh
H 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 rats
P B Mortensen, N Gregersen
Pediatric Research
|
September 1, 1979
Ketotic episodes in glutaryl-CoA dehydrogenase deficiency (glutaric aciduria)
N Gregersen, N J Brandt
Page
of 21
Search research articles
Search
Showing results (11-20 of 208) with videos related to
Sort By:
Page
of 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 newborn
N 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 liver
S 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 lines
N Gregersen, S Kølvraa
Biochimica Et Biophysica Acta
|
May 21, 1986
In vitro studies on the oxidation of medium-chain dicarboxylic acids in rat liver
S 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 acidurias
P 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 rats
P B Mortensen, N Gregersen
Scandinavian Journal of Plastic and Reconstructive Surgery
|
January 1, 1986
Giant incisional hernias closed with polypropylene mesh
H 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 rats
P B Mortensen, N Gregersen
Pediatric Research
|
September 1, 1979
Ketotic episodes in glutaryl-CoA dehydrogenase deficiency (glutaric aciduria)
N Gregersen, N J Brandt
Page
of 21