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N Gregersen

Showing results (121-130 of 208) with videos related to

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Ugeskrift for Laeger|February 17, 1992
[Medium chain acyl-CoA dehydrogenase (MCAD) deficiency: a life-threatening defect of fatty acid oxidation]N Gregersen, V Winter, B S Andresen, et al.
The Journal of Pediatrics|April 11, 2001
Acute fatty liver of pregnancy associated with short-chain acyl-coenzyme A dehydrogenase deficiencyD Matern, P Hart, A P Murtha, et al.
Acta Paediatrica Scandinavica|November 1, 1983
Dicarboxylic aciduria due to medium chain acyl CoA dehydrogenase defect. A cause of hypoglycemia in childhoodP Divry, M David, N Gregersen, et al.
Acta Paediatrica (Oslo, Norway : 1992)|June 1, 1993
The frequency of a disease-causing point mutation in the gene coding for medium-chain acyl-CoA dehydrogenase in sudden infant death syndromeJ B Lundemose, N Gregersen, S Kølvraa, et al.
Human Mutation|July 20, 2001
Detection of mutations in the COL4A5 gene by SSCP in X-linked Alport syndromeJ M Hertz, I Juncker, U Persson, et al.
Clinical Genetics|June 1, 1990
In situ hybridization analysis of isodicentric X-chromosomes with short arm fusionJ E Koch, S Kølvraa, J M Hertz, et al.
Physical Review Letters|March 10, 2012
Bloch-wave engineering of quantum dot micropillars for cavity quantum electrodynamics experimentsM Lermer, N Gregersen, F Dunzer, et al.
Current Pharmaceutical Design|April 15, 2010
Anti-inflammatory heat shock protein 70 genes are positively associated with human survivalR Singh, S Kølvraa, P Bross, et al.
Scandinavian Journal of Clinical and Laboratory Investigation. Supplementum|January 1, 1995
Molecular diagnosis and characterization of medium-chain acyl-CoA dehydrogenase deficiencyB S Andresen, P Bross, T G Jensen, et al.
Journal of Proteomics|May 21, 2011
Characterization of mitochondrial proteome in a severe case of ETF-QO deficiencyH Rocha, R Ferreira, J Carvalho, et al.
Pageof 21

Showing results (121-130 of 208) with videos related to

Sort By:
Pageof 21
Ugeskrift for Laeger|February 17, 1992
[Medium chain acyl-CoA dehydrogenase (MCAD) deficiency: a life-threatening defect of fatty acid oxidation]N Gregersen, V Winter, B S Andresen, et al.
The Journal of Pediatrics|April 11, 2001
Acute fatty liver of pregnancy associated with short-chain acyl-coenzyme A dehydrogenase deficiencyD Matern, P Hart, A P Murtha, et al.
Acta Paediatrica Scandinavica|November 1, 1983
Dicarboxylic aciduria due to medium chain acyl CoA dehydrogenase defect. A cause of hypoglycemia in childhoodP Divry, M David, N Gregersen, et al.
Acta Paediatrica (Oslo, Norway : 1992)|June 1, 1993
The frequency of a disease-causing point mutation in the gene coding for medium-chain acyl-CoA dehydrogenase in sudden infant death syndromeJ B Lundemose, N Gregersen, S Kølvraa, et al.
Human Mutation|July 20, 2001
Detection of mutations in the COL4A5 gene by SSCP in X-linked Alport syndromeJ M Hertz, I Juncker, U Persson, et al.
Clinical Genetics|June 1, 1990
In situ hybridization analysis of isodicentric X-chromosomes with short arm fusionJ E Koch, S Kølvraa, J M Hertz, et al.
Physical Review Letters|March 10, 2012
Bloch-wave engineering of quantum dot micropillars for cavity quantum electrodynamics experimentsM Lermer, N Gregersen, F Dunzer, et al.
Current Pharmaceutical Design|April 15, 2010
Anti-inflammatory heat shock protein 70 genes are positively associated with human survivalR Singh, S Kølvraa, P Bross, et al.
Scandinavian Journal of Clinical and Laboratory Investigation. Supplementum|January 1, 1995
Molecular diagnosis and characterization of medium-chain acyl-CoA dehydrogenase deficiencyB S Andresen, P Bross, T G Jensen, et al.
Journal of Proteomics|May 21, 2011
Characterization of mitochondrial proteome in a severe case of ETF-QO deficiencyH Rocha, R Ferreira, J Carvalho, et al.
Pageof 21