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Published in Clinical cancer research (01.12.2000)
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Published in Human molecular genetics (01.12.2005)
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Cardiolipin deficiency in x-linked cardioskeletal myopathy and neutropenia (barth syndrome, mim 302060): a study in cultured skin fibroblasts
Valianpour, Fredoen, Wanders, Ronald J.A., Overmars, Henk, Vreken, Peter, van Gennip, Albert H., Baas, Frank, Plecko, Barbara, Santer, Rene, Becker, Kolja, Barth, Peter G.
Published in The Journal of pediatrics (01.11.2002)
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Peroxisomal D-hydroxyacyl-CoA Dehydrogenase Deficiency: Resolution of the Enzyme Defect and Its Molecular Basis in Bifunctional Protein Deficiency
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Published in Proceedings of the National Academy of Sciences - PNAS (03.03.1998)
Published in Proceedings of the National Academy of Sciences - PNAS (03.03.1998)
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Dihydropyrimidine dehydrogenase pharmacogenetics in Caucasian subjects
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Published in British journal of clinical pharmacology (01.08.1998)
Published in British journal of clinical pharmacology (01.08.1998)
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Dihydropyrimidinase Deficiency: Structural Organization, Chromosomal Localization, and Mutation Analysis of the Human Dihydropyrimidinase Gene
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Published in American journal of human genetics (01.09.1998)
Published in American journal of human genetics (01.09.1998)
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Defective Remodeling of Cardiolipin and Phosphatidylglycerol in Barth Syndrome
Vreken, Peter, Valianpour, Fredoen, Nijtmans, Leo G., Grivell, Les A., Plecko, Barbara, Wanders, Ronald J.A., Barth, Peter G.
Published in Biochemical and biophysical research communications (20.12.2000)
Published in Biochemical and biophysical research communications (20.12.2000)
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Significantly reduced docosahexaenoic and docosapentaenoic acid concentrations in erythrocyte membranes from schizophrenic patients compared with a carefully matched control group
Assies, Johanna, Lieverse, Ritsaert, Vreken, Peter, Wanders, Ron J.A, Dingemans, Peter M.J.A, Linszen, Donald H
Published in Biological psychiatry (1969) (15.03.2001)
Published in Biological psychiatry (1969) (15.03.2001)
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Mutations in the gene encoding peroxisomal α-methylacyl-CoA racemase cause adult-onset sensory motor neuropathy
Wanders, Ronald J.A, Ferdinandusse, Sacha, Denis, Simone, Clayton, Peter T, Graham, Andrew, Rees, John E, Allen, John T, McLean, Brendan N, Brown, Ann Y, Vreken, Peter, Waterham, Hans R
Published in Nature genetics (01.02.2000)
Published in Nature genetics (01.02.2000)
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Smith-Lemli-Opitz Syndrome Is Caused by Mutations in the 7-Dehydrocholesterol Reductase Gene
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Published in American journal of human genetics (01.08.1998)
Published in American journal of human genetics (01.08.1998)
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Short-chain Acyl-CoA dehydrogenase deficiency: studies in a large family adding to the complexity of the disorder
Bok, Levinus A, Vreken, Peter, Wijburg, Frits A, Wanders, Ronald J A, Gregersen, Niels, Corydon, Morten J, Waterham, Hans R, Duran, Marinus
Published in Pediatrics (Evanston) (01.11.2003)
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Plasmalogen Phospholipids Are Involved in HDL-Mediated Cholesterol Efflux: Insights from Investigations with Plasmalogen-Deficient Cells
Mandel, Hanna, Sharf, Rakefet, Berant, Moshe, Wanders, Ronald J.A., Vreken, Peter, Aviram, Michael
Published in Biochemical and biophysical research communications (18.09.1998)
Published in Biochemical and biophysical research communications (18.09.1998)
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β-Ureidopropionase deficiency: A novel inborn error of metabolism discovered using NMR spectroscopy on urine
Moolenaar, Sytske H., Göhlich-Ratmann, Gudrun, Engelke, Udo F.H., Spraul, Manfred, Humpfer, Eberhard, Dvortsak, Peter, Voit, Thomas, Hoffmann, Georg F., Bräutigam, Christa, van Kuilenburg, André B., van Gennip, Albert, Vreken, Peter, Wevers, Ron A.
Published in Magnetic resonance in medicine (01.11.2001)
Published in Magnetic resonance in medicine (01.11.2001)
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X-linked cardioskeletal myopathy and neutropenia (Barth syndrome)—MIM 302060
Barth, Peter G., Wanders, Ronald J.A., Vreken, Peter
Published in The Journal of pediatrics (01.09.1999)
Published in The Journal of pediatrics (01.09.1999)
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Analysis of Carnitine Biosynthesis Metabolites in Urine by HPLC-Electrospray Tandem Mass Spectrometry
Vaz, Frederic M, Melegh, Bela, Bene, Judit, Cuebas, Dean, Gage, Douglas A, Bootsma, Albert, Vreken, Peter, van Gennip, Albert H, Bieber, Loran L, Wanders, Ronald J.A
Published in Clinical chemistry (Baltimore, Md.) (01.06.2002)
Published in Clinical chemistry (Baltimore, Md.) (01.06.2002)
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Carbohydrate-deficient glycoprotein syndrome type 1a: A variant phenotype with borderline cognitive dysfunction, cerebellar hypoplasia, and coagulation disturbances
van Ommen, C.Heleen, Peters, Marjolein, Barth, Peter G., Vreken, Peter, Wanders, Ron J.A., Jaeken, Joak
Published in The Journal of pediatrics (01.03.2000)
Published in The Journal of pediatrics (01.03.2000)
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Sztriha, László, Gururaj, Aithala, Vreken, Peter, Nork, Michael, Lestringant, Gilles G
Published in Pediatric neurology (01.08.2002)
Published in Pediatric neurology (01.08.2002)
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Effect of dehydroepiandrosterone (DHEA) supplementation on fatty acid and hormone levels in patients with X-linked adrenoleukodystrophy
Assies, Johanna, Haverkort, Elisabeth B, Lieverse, Ritsaert, Vreken, Peter
Published in Advances in experimental medicine and biology (2003)
Published in Advances in experimental medicine and biology (2003)
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