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Morten Corydon

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Chemicals & Drugs

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Inborn Errors Lipid Metabolism

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Levinus A Bok; Peter Vreken; Frits A Wijburg; Ronald J A Wanders; Niels Gregersen; Morten J Corydon; Hans R Waterham; Marinus Duran
Short-chain Acyl-CoA dehydrogenase deficiency: studies in a large family adding to the complexity of the disorder.
Niels Gregersen; Brage S Andresen; Morten J Corydon; Thomas J Corydon; Rikke K J Olsen; Lars Bolund; Peter Bross
Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship.
Morten J Corydon; Jerry Vockley; Piero Rinaldo; William J Rhead; M Kjeldsen; Vibeke Winter; C Riggs; Dusica Babovic-Vuksanovic; jan smeitink; J De Jong; H Levy; Adrian C Sewell; Charles R Roe; Dietrich Matern; M Dasouki; Niels Gregersen
Role of common gene variations in the molecular pathogenesis of short-chain acyl-CoA dehydrogenase deficiency.

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All Publications

2003: Levinus A Bok; Peter Vreken; Frits A Wijburg; Ronald J A Wanders; Niels Gregersen; Morten J Corydon; Hans R Waterham; Marinus Duran
Short-chain Acyl-CoA dehydrogenase deficiency: studies in a large family adding to the complexity of the disorder.
Pediatrics 2003;112(5):1152-5.
2001: Niels Gregersen; Brage S Andresen; Morten J Corydon; Thomas J Corydon; Rikke K J Olsen; Lars Bolund; Peter Bross
Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship.
Human mutation 2001;18(3):169-89.
2001: Morten J Corydon; Jerry Vockley; Piero Rinaldo; William J Rhead; M Kjeldsen; Vibeke Winter; C Riggs; Dusica Babovic-Vuksanovic; jan smeitink; J De Jong; H Levy; Adrian C Sewell; Charles R Roe; Dietrich Matern; M Dasouki; Niels Gregersen
Role of common gene variations in the molecular pathogenesis of short-chain acyl-CoA dehydrogenase deficiency.
Pediatric research 2001;49(1):18-23.
1999: Peter Bross; Palle Lyngsie Pedersen; Vibeke Winter; M Nyholm; B N Johansen; Rikke K J Olsen; Morten J Corydon; Brage S Andresen; Hans Eiberg; S Kolvraa; Niels Gregersen
A polymorphic variant in the human electron transfer flavoprotein alpha-chain (alpha-T171) displays decreased thermal stability and is overrepresented in very-long-chain acyl-CoA dehydrogenase-deficient patients with mild childhood presentation.
Molecular genetics and metabolism 1999;67(2):138-47.
1999: Xiuqing Zhang; Huanming Yang; Morten J Corydon; X Zhang; S Pedersen; Julie R Korenberg; Xiao-Ning Chen; J Laporte; Niels Gregersen; Erik Niebuhr; G Liu; Lars Bolund
Localization of a human nucleoporin 155 gene (NUP155) to the 5p13 region and cloning of its cDNA.
Genomics 1999;57(1):144-51.
1998: Thomas J Corydon; Peter Bross; Thomas G Jensen; Morten J Corydon; T B Lund; Uffe B Jensen; J J Kim; Niels Gregersen; Lars Bolund
Rapid degradation of short-chain acyl-CoA dehydrogenase variants with temperature-sensitive folding defects occurs after import into mitochondria.
The Journal of biological chemistry 1998;273(21):13065-71.
1998: Niels Gregersen; Vibeke Winter; Morten J Corydon; Thomas J Corydon; Piero Rinaldo; Antonia Ribes; G Martinez; M J Bennett; Christine Vianey-Saban; A Bhala; Daniel Hale; Willy Lehnert; S Kmoch; Manuel Roig; Encarnació Riudor; Hans Eiberg; Brage S Andresen; Peter Bross; Lars Bolund; Steen Kølvraa
Identification of four new mutations in the short-chain acyl-CoA dehydrogenase (SCAD) gene in two patients: one of the variant alleles, 511C-->T, is present at an unexpectedly high frequency in the general population, as was the case for 625G-->A, together conferring susceptibility to ethylmalonic aciduria.
Human molecular genetics 1998;7(4):619-27.
1997: Morten J Corydon; Brage S Andresen; Peter Bross; M Kjeldsen; PH Andreasen; Hans Eiberg; Steen Kølvraa; Niels Gregersen
Structural organization of the human short-chain acyl-CoA dehydrogenase gene.
Mammalian genome : official journal of the International Mammalian Genome Society 1997;8(12):922-6.
1997: Henrik K Jensen; Thomas G Jensen; Ole Faergeman; Lillian G Jensen; Brage S Andresen; Morten J Corydon; PH Andreasen; PS Hansen; F Heath; Lars Bolund; Niels Gregersen
Two mutations in the same low-density lipoprotein receptor allele act in synergy to reduce receptor function in heterozygous familial hypercholesterolemia.
Human mutation 1997;9(5):437-44.
1996: Morten J Corydon; Niels Gregersen; W Lehnert; Antonia Ribes; P Rinaldo; Stanislav Kmoch; E Christensen; T J Kristensen; Brage S Andresen; Peter Bross; Vibeke Winter; G Martinez; Søren Neve; Thomas G Jensen; Lars Bolund; Steen Kølvraa
Ethylmalonic aciduria is associated with an amino acid variant of short chain acyl-coenzyme A dehydrogenase.
Pediatric research 1996;39(6):1059-66.
1996: Brage S Andresen; Peter Bross; Christine Vianey-Saban; Priscille Divry; Marie-Therese Zabot; Charles R Roe; M A Nada; A Byskov; Torben A Kruse; Søren Neve; Karsten Kristiansen; I Knudsen; Morten J Corydon; Niels Gregersen
Cloning and characterization of human very-long-chain acyl-CoA dehydrogenase cDNA, chromosomal assignment of the gene and identification in four patients of nine different mutations within the VLCAD gene.
Human molecular genetics 1996;5(4):461-72.