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The Journal of Pediatrics|March 4, 2000
Carbohydrate-deficient glycoprotein syndrome type 1a: a variant phenotype with borderline cognitive dysfunction, cerebellar hypoplasia, and coagulation disturbancesC H van Ommen, M Peters, P G Barth, et al.
Thrombosis and Haemostasis|August 1, 1995
A point mutation in an invariant splice acceptor site results in a decreased mRNA level in a patient with severe coagulation factor XIII subunit A deficiencyP Vreken, R W Niessen, M Peters, et al.
Biological Chemistry|March 4, 1999
Cytidine triphosphate synthase activity and mRNA expression in normal human blood cellsA C Verschuur, A H Van Gennip, E J Muller, et al.
Journal of Inherited Metabolic Disease|July 17, 1999
Disorders of mitochondrial fatty acyl-CoA beta-oxidationR J Wanders, P Vreken, M E den Boer, et al.
Biochemical and Biophysical Research Communications|December 19, 2000
Defective remodeling of cardiolipin and phosphatidylglycerol in Barth syndromeP Vreken, F Valianpour, L G Nijtmans, et al.
Biochimie|June 1, 1991
Turnover rate of yeast PGK mRNA can be changed by specific alterations in its trailer structureP Vreken, R van der Veen, V C de Regt, et al.
Yeast (Chichester, England)|June 1, 1993
Known heat-shock proteins are not responsible for stress-induced rapid degradation of ribosomal protein mRNAs in yeastL Galego, I Barahona, A P Alves, et al.
Advances in Experimental Medicine and Biology|March 10, 2000
Rapid diagnosis of organic acidemias and fatty-acid oxidation defects by quantitative electrospray tandem-MS acyl-carnitine analysis in plasmaP Vreken, A E van Lint, A H Bootsma, et al.
European Journal of Pediatrics|September 15, 1999
Cerebral palsy and pyruvate dehydrogenase deficiency: identification of two new mutations in the E1alpha geneW Lissens, P Vreken, P G Barth, et al.
Biochemical Society Transactions|May 18, 2001
Peroxisomal fatty acid alpha- and beta-oxidation in humans: enzymology, peroxisomal metabolite transporters and peroxisomal diseasesR J Wanders, P Vreken, S Ferdinandusse, et al.
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