Mooyer P - Search Results

1

Elongation of very long-chain fatty acids is enhanced in X-linked adrenoleukodystrophy.

Kemp S, Valianpour F, Denis S, Ofman R, Sanders RJ, Mooyer P, Barth PG, Wanders RJ. Kemp S, et al. Among authors: mooyer p. Mol Genet Metab. 2005 Feb;84(2):144-51. doi: 10.1016/j.ymgme.2004.09.015. Mol Genet Metab. 2005. PMID: 15670720

2

Method for measurement of peroxisomal very-long-chain fatty acid beta-oxidation in human skin fibroblasts using stable-isotope-labeled tetracosanoic acid.

Kemp S, Valianpour F, Mooyer PA, Kulik W, Wanders RJ. Kemp S, et al. Clin Chem. 2004 Oct;50(10):1824-6. doi: 10.1373/clinchem.2004.038539. Clin Chem. 2004. PMID: 15388659 No abstract available.

3

ACBD5 deficiency causes a defect in peroxisomal very long-chain fatty acid metabolism.

Ferdinandusse S, Falkenberg KD, Koster J, Mooyer PA, Jones R, van Roermund CWT, Pizzino A, Schrader M, Wanders RJA, Vanderver A, Waterham HR. Ferdinandusse S, et al. Among authors: mooyer pa. J Med Genet. 2017 May;54(5):330-337. doi: 10.1136/jmedgenet-2016-104132. Epub 2016 Oct 31. J Med Genet. 2017. PMID: 27799409

4

Impaired neuronal migration and endochondral ossification in Pex7 knockout mice: a model for rhizomelic chondrodysplasia punctata.

Brites P, Motley AM, Gressens P, Mooyer PA, Ploegaert I, Everts V, Evrard P, Carmeliet P, Dewerchin M, Schoonjans L, Duran M, Waterham HR, Wanders RJ, Baes M. Brites P, et al. Among authors: mooyer pa. Hum Mol Genet. 2003 Sep 15;12(18):2255-67. doi: 10.1093/hmg/ddg236. Epub 2003 Jul 15. Hum Mol Genet. 2003. PMID: 12915479

5

Clinical and biochemical spectrum of D-bifunctional protein deficiency.

Ferdinandusse S, Denis S, Mooyer PA, Dekker C, Duran M, Soorani-Lunsing RJ, Boltshauser E, Macaya A, Gärtner J, Majoie CB, Barth PG, Wanders RJ, Poll-The BT. Ferdinandusse S, et al. Among authors: mooyer pa. Ann Neurol. 2006 Jan;59(1):92-104. doi: 10.1002/ana.20702. Ann Neurol. 2006. PMID: 16278854

6

Genotype-phenotype correlation in PEX5-deficient peroxisome biogenesis defective cell lines.

Ebberink MS, Mooyer PA, Koster J, Dekker CJ, Eyskens FJ, Dionisi-Vici C, Clayton PT, Barth PG, Wanders RJ, Waterham HR. Ebberink MS, et al. Among authors: mooyer pa. Hum Mutat. 2009 Jan;30(1):93-8. doi: 10.1002/humu.20833. Hum Mutat. 2009. PMID: 18712838

7

Plasmalogens participate in very-long-chain fatty acid-induced pathology.

Brites P, Mooyer PA, El Mrabet L, Waterham HR, Wanders RJ. Brites P, et al. Among authors: mooyer pa. Brain. 2009 Feb;132(Pt 2):482-92. doi: 10.1093/brain/awn295. Epub 2008 Nov 20. Brain. 2009. PMID: 19022859

8

ALDP expression in fibroblasts of patients with X-linked adrenoleukodystrophy.

Kemp S, Mooyer PA, Bolhuis PA, van Geel BM, Mandel JL, Barth PG, Aubourg P, Wanders RJ. Kemp S, et al. Among authors: mooyer pa. J Inherit Metab Dis. 1996;19(5):667-74. doi: 10.1007/BF01799844. J Inherit Metab Dis. 1996. PMID: 8892025

9

A lethal defect of mitochondrial and peroxisomal fission.

Waterham HR, Koster J, van Roermund CW, Mooyer PA, Wanders RJ, Leonard JV. Waterham HR, et al. Among authors: mooyer pa. N Engl J Med. 2007 Apr 26;356(17):1736-41. doi: 10.1056/NEJMoa064436. N Engl J Med. 2007. PMID: 17460227 Free article.

10

D-2-hydroxyglutaric acidaemia: identification of a new enzyme, D-2-hydroxyglutarate dehydrogenase, localized in mitochondria.

Wanders RJ, Mooyer P. Wanders RJ, et al. Among authors: mooyer p. J Inherit Metab Dis. 1995;18(2):194-6. doi: 10.1007/BF00711764. J Inherit Metab Dis. 1995. PMID: 7564244 No abstract available.

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