Publications by authors named "Peter Vreken"

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Inactivation of the peroxisomal ABCD2 transporter in the mouse leads to late-onset ataxia involving mitochondria, Golgi and endoplasmic reticulum damage.
Isidre Ferrer, Josef P Kapfhammer, Colette Hindelang, Stephan Kemp, Nathalie Troffer-Charlier, Peter Vreken

Hum Mol Genet· December 2005

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Effect of dehydroepiandrosterone (DHEA) supplementation on fatty acid and hormone levels in patients with X-linked adrenoleukodystrophy.
Johanna Assies, Elisabeth B Haverkort, Ritsaert Lieverse, Peter Vreken

Adv Exp Med Biol· July 2004

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Short-chain Acyl-CoA dehydrogenase deficiency: studies in a large family adding to the complexity of the disorder.
Levinus A Bok, Peter Vreken, Frits A Wijburg, Ronald J A Wanders, Niels Gregersen

Pediatrics· November 2003

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Cardiolipin deficiency in X-linked cardioskeletal myopathy and neutropenia (Barth syndrome, MIM 302060): a study in cultured skin fibroblasts.
Fredoen Valianpour, Ronald J A Wanders, Henk Overmars, Peter Vreken, Albert H Van Gennip

J Pediatr· November 2002

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L-2-hydroxyglutaric aciduria in two siblings.
László Sztriha, Aithala Gururaj, Peter Vreken, Michael Nork, Gilles Lestringant

Pediatr Neurol· August 2002

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Analysis of carnitine biosynthesis metabolites in urine by HPLC-electrospray tandem mass spectrometry.
Frédéric M Vaz, Bela Melegh, Judit Bene, Dean Cuebas, Douglas A Gage, Peter Vreken

Clin Chem· June 2002

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