Gregersen N - Search Results

1

Variants in the ethylmalonyl-CoA decarboxylase (ECHDC1) gene: a novel player in ethylmalonic aciduria?

Fogh S, Dipace G, Bie A, Veiga-da-Cunha M, Hansen J, Kjeldsen M, Mosegaard S, Ribes A, Gregersen N, Aagaard L, Van Schaftingen E, Olsen RKJ. Fogh S, et al. Among authors: gregersen n. J Inherit Metab Dis. 2021 Sep;44(5):1215-1225. doi: 10.1002/jimd.12394. Epub 2021 Jun 8. J Inherit Metab Dis. 2021. PMID: 33973257 Free PMC article.

2

Mitochondrial fatty acid oxidation defects--remaining challenges.

Gregersen N, Andresen BS, Pedersen CB, Olsen RK, Corydon TJ, Bross P. Gregersen N, et al. J Inherit Metab Dis. 2008 Oct;31(5):643-57. doi: 10.1007/s10545-008-0990-y. Epub 2008 Oct 7. J Inherit Metab Dis. 2008. PMID: 18836889

3

Disease mechanisms and protein structures in fatty acid oxidation defects.

Gregersen N, Olsen RK. Gregersen N, et al. J Inherit Metab Dis. 2010 Oct;33(5):547-53. doi: 10.1007/s10545-010-9046-1. Epub 2010 Feb 12. J Inherit Metab Dis. 2010. PMID: 20151199

4

Antioxidant dysfunction: potential risk for neurotoxicity in ethylmalonic aciduria.

Pedersen CB, Zolkipli Z, Vang S, Palmfeldt J, Kjeldsen M, Stenbroen V, Schmidt SP, Wanders RJ, Ruiter JP, Wibrand F, Tein I, Gregersen N. Pedersen CB, et al. Among authors: gregersen n. J Inherit Metab Dis. 2010 Jun;33(3):211-22. doi: 10.1007/s10545-010-9086-6. Epub 2010 May 5. J Inherit Metab Dis. 2010. PMID: 20443061

5

High-resolution melting analysis, a simple and effective method for reliable mutation scanning and frequency studies in the ACADVL gene.

Olsen RK, Dobrowolski SF, Kjeldsen M, Hougaard D, Simonsen H, Gregersen N, Andresen BS. Olsen RK, et al. Among authors: gregersen n. J Inherit Metab Dis. 2010 Jun;33(3):247-60. doi: 10.1007/s10545-010-9101-y. Epub 2010 May 18. J Inherit Metab Dis. 2010. PMID: 20480395

6

Mitochondrial proteomics--a tool for the study of metabolic disorders.

Gregersen N, Hansen J, Palmfeldt J. Gregersen N, et al. J Inherit Metab Dis. 2012 Jul;35(4):715-26. doi: 10.1007/s10545-012-9480-3. Epub 2012 Apr 17. J Inherit Metab Dis. 2012. PMID: 22526845 Review.

7

Proteomic investigation of cultivated fibroblasts from patients with mitochondrial short-chain acyl-CoA dehydrogenase deficiency.

Edhager AV, Stenbroen V, Nielsen NS, Bross P, Olsen RKJ, Gregersen N, Palmfeldt J. Edhager AV, et al. Among authors: gregersen n. Mol Genet Metab. 2014 Mar;111(3):360-368. doi: 10.1016/j.ymgme.2014.01.007. Epub 2014 Jan 24. Mol Genet Metab. 2014. PMID: 24485985

8

Redox signalling and mitochondrial stress responses; lessons from inborn errors of metabolism.

Olsen RK, Cornelius N, Gregersen N. Olsen RK, et al. Among authors: gregersen n. J Inherit Metab Dis. 2015 Jul;38(4):703-19. doi: 10.1007/s10545-015-9861-5. Epub 2015 May 30. J Inherit Metab Dis. 2015. PMID: 26025548 Free PMC article. Review.

9

Riboflavin Deficiency-Implications for General Human Health and Inborn Errors of Metabolism.

Mosegaard S, Dipace G, Bross P, Carlsen J, Gregersen N, Olsen RKJ. Mosegaard S, et al. Among authors: gregersen n. Int J Mol Sci. 2020 May 28;21(11):3847. doi: 10.3390/ijms21113847. Int J Mol Sci. 2020. PMID: 32481712 Free PMC article. Review.

10

Structural organization of the human short-chain acyl-CoA dehydrogenase gene.

Corydon MJ, Andresen BS, Bross P, Kjeldsen M, Andreasen PH, Eiberg H, Kølvraa S, Gregersen N. Corydon MJ, et al. Among authors: gregersen n. Mamm Genome. 1997 Dec;8(12):922-6. doi: 10.1007/s003359900612. Mamm Genome. 1997. PMID: 9383286

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