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Results: 1-11 |
Results: 11

Authors: Willemsen, MAAP Rotteveel, JJ de Jong, JGN Wanders, RJA IJlst, L Hoffmann, GF Mayatepek, E
Citation: Maap. Willemsen et al., Defective metabolism of Leukotriene B-4 in the Sjogren-Larsson Syndrome, J NEUR SCI, 183(1), 2001, pp. 61-67

Authors: Silva, MFB Ruiter, JPN IJlst, L Jakobs, C Duran, M de Almeida, IT Wanders, RJA
Citation: Mfb. Silva et al., Differential effect of valproate and its Delta(2)- and Delta(4)-unsaturated metabolites, on the beta-oxidation rate of long-chain and medium-chain fatty acids, CHEM-BIO IN, 137(3), 2001, pp. 203-212

Authors: Silva, MFB Ruiter, JPN IJlst, L Allers, P ten Brink, HJ Jakobs, C Duran, M de Almedia, IT Wander, RJA
Citation: Mfb. Silva et al., Synthesis and intramitochondrial levels of valproyl-coenzyme A metabolites, ANALYT BIOC, 290(1), 2001, pp. 60-67

Authors: Roschinger, W Muntau, AC Duran, M Dorland, L IJlst, L Wanders, RJA Roscher, AA
Citation: W. Roschinger et al., Carnitine-acylcarnitine translocase deficiency: metabolic consequences of an impaired mitochondrial carnitine cycle, CLIN CHIM A, 298(1-2), 2000, pp. 55-68

Authors: IJlst, L de Kromme, I Oostheim, W Wanders, RJA
Citation: L. Ijlst et al., Molecular cloning and expression of human L-pipecolate oxidase, BIOC BIOP R, 270(3), 2000, pp. 1101-1105

Authors: Bennett, MJ Spotswood, SD Ross, KF Comfort, S Koonce, R Boriack, RL IJlst, L Wanders, RJA
Citation: Mj. Bennett et al., Fatal hepatic short-chain L-3-hydroxyacyl-coenzyme A dehydrogenase deficiency: Clinical, biochemical, and pathological studies on three subjects withthis recently identified disorder of mitochondrial beta-oxidation, PEDIATR D P, 2(4), 1999, pp. 337-345

Authors: de Jongh, S Vreken, P IJlst, L Wanders, RJA Jakobs, C Bakker, HD
Citation: S. De Jongh et al., Spontaneous pregnancy in a patient with classical galactosaemia, J INH MET D, 22(6), 1999, pp. 754-755

Authors: Wanders, RJA Vreken, P den Boer, MEJ Wijburg, FA van Gennip, AH IJlst, L
Citation: Rja. Wanders et al., Disorders of mitochondrial fatty acyl-CoA beta-oxidation, J INH MET D, 22(4), 1999, pp. 442-487

Authors: Andresen, BS Olpin, S Kvittingen, EA Augoustides-Savvopoulou, P Lindhout, D Halley, DJJ Vianey-Saban, C Wanders, RJA IJlst, L Schroeder, LD Bolund, L Gregersen, N
Citation: Bs. Andresen et al., DNA-based prenatal diagnosis for very-long-chain acyl-CoA dehydrogenase deficiency, J INH MET D, 22(3), 1999, pp. 281-285

Authors: IJlst, L Oostheim, W van Werkhoven, M Willemsen, MAAP Wanders, RJA
Citation: L. Ijlst et al., Molecular basis of Sjogren-Larsson syndrome: Frequency of the 1297-1298 del GA and 943C -> T mutation in 29 patients, J INH MET D, 22(3), 1999, pp. 319-321

Authors: Ferdinandusse, S Mulders, J IJlst, L Denis, S Dacremont, G Waterham, HR Wanders, RJA
Citation: S. Ferdinandusse et al., Molecular cloning and expression of human carnitine octanoyltransferase: Evidence for its role in the peroxisomal beta-oxidation of branched-chain fatty acids, BIOC BIOP R, 263(1), 1999, pp. 213-218
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