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N Gregersen

Showing results (21-30 of 208) with videos related to

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Pediatric Research|July 1, 1984
Glutaric aciduria type II: evidence for a defect related to the electron transfer flavoprotein or its dehydrogenaseE Christensen, S Kølvraa, N Gregersen
Journal of Inherited Metabolic Disease|January 1, 1984
In vivo studies on the metabolic derangement in a patient with D-glyceric acidaemia and hyperglycinaemiaS Kølvraa, N Gregersen, E Christensen
Acta Paediatrica Scandinavica|January 1, 1977
Low molecular weight organic acids in the urine of the newbornN Gregersen, J Ingerslev, K Rasmussen
Clinical Genetics|November 1, 1977
Congenital malformation of the feet with low body height. A new syndrome, caused by an autosomal dominant geneH N Gregersen, G B Petersen
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 2, 1976
Suberylglycine excretion in the urine from a patient with dicarboxylic aciduriaN Gregersen, R Lauritzen, K Rasmussen
Biomedical Mass Spectrometry|October 1, 1979
N-acylglycines: gas chromatographic mass spectrometric identification and determination in urine by selected ion monitoringN Gregersen, K Keiding, S Kølvraa
Progress in Clinical and Biological Research|January 1, 1990
Riboflavin responsive glutaric aciduria type IIN Gregersen, W Rhead, E Christensen
Progress in Nucleic Acid Research and Molecular Biology|October 6, 1997
Impaired folding and subunit assembly as disease mechanism: the example of medium-chain acyl-CoA dehydrogenase deficiencyP Bross, B S Andresen, N Gregersen
Journal of Medical Genetics|July 1, 1991
Normal MPS excretion, but dermatan sulphaturia, combined with a mild Maroteaux-Lamy phenotypeT Tønnesen, H N Gregersen, F Güttler
Journal of Inherited Metabolic Disease|January 1, 1978
N-Dicarboxylmonoglycines: excretion in dicarboxylic acidurias and mode of formationI H Grøn, N Gregersen, K Rasmussen
Pageof 21

Showing results (21-30 of 208) with videos related to

Sort By:
Pageof 21
Pediatric Research|July 1, 1984
Glutaric aciduria type II: evidence for a defect related to the electron transfer flavoprotein or its dehydrogenaseE Christensen, S Kølvraa, N Gregersen
Journal of Inherited Metabolic Disease|January 1, 1984
In vivo studies on the metabolic derangement in a patient with D-glyceric acidaemia and hyperglycinaemiaS Kølvraa, N Gregersen, E Christensen
Acta Paediatrica Scandinavica|January 1, 1977
Low molecular weight organic acids in the urine of the newbornN Gregersen, J Ingerslev, K Rasmussen
Clinical Genetics|November 1, 1977
Congenital malformation of the feet with low body height. A new syndrome, caused by an autosomal dominant geneH N Gregersen, G B Petersen
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 2, 1976
Suberylglycine excretion in the urine from a patient with dicarboxylic aciduriaN Gregersen, R Lauritzen, K Rasmussen
Biomedical Mass Spectrometry|October 1, 1979
N-acylglycines: gas chromatographic mass spectrometric identification and determination in urine by selected ion monitoringN Gregersen, K Keiding, S Kølvraa
Progress in Clinical and Biological Research|January 1, 1990
Riboflavin responsive glutaric aciduria type IIN Gregersen, W Rhead, E Christensen
Progress in Nucleic Acid Research and Molecular Biology|October 6, 1997
Impaired folding and subunit assembly as disease mechanism: the example of medium-chain acyl-CoA dehydrogenase deficiencyP Bross, B S Andresen, N Gregersen
Journal of Medical Genetics|July 1, 1991
Normal MPS excretion, but dermatan sulphaturia, combined with a mild Maroteaux-Lamy phenotypeT Tønnesen, H N Gregersen, F Güttler
Journal of Inherited Metabolic Disease|January 1, 1978
N-Dicarboxylmonoglycines: excretion in dicarboxylic acidurias and mode of formationI H Grøn, N Gregersen, K Rasmussen
Pageof 21