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	1.	Disorders of mitochondrial fatty acyl-CoA beta-oxidation. [electronic resource] by Wanders, R J Vreken, P den Boer, M E Wijburg, F A van Gennip, A H IJlst, L Producer: 19990923 In: Journal of inherited metabolic disease vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Heterozygosity for the common LCHAD mutation (1528g>C) is not a major cause of HELLP syndrome and the prevalence of the mutation in the Dutch population is low. [electronic resource] by den Boer, M E Ijlst, L Wijburg, F A Oostheim, W van Werkhoven, M A van Pampus, M G Heymans, H S Wanders, R J Producer: 20001120 In: Pediatric research vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	High activity of fatty acid oxidation enzymes in human placenta: implications for fetal-maternal disease. [electronic resource] by Oey, N A den Boer, M E J Ruiter, J P N Wanders, R J A Duran, M Waterham, H R Boer, K van der Post, J A M Wijburg, F A Producer: 20040401 In: Journal of inherited metabolic disease vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Bone mineral density in children and adolescents with Prader-Willi syndrome: a longitudinal study during puberty and 9 years of growth hormone treatment. [electronic resource] by Bakker, N E Kuppens, R J Siemensma, E P C Tummers-de Lind van Wijngaarden, R F A Festen, D A M Bindels-de Heus, G C B Bocca, G Haring, D A J P Hoorweg-Nijman, J J G Houdijk, E C A M Jira, P E Lunshof, L Odink, R J Oostdijk, W Rotteveel, J Van Alfen, A A E M Van Leeuwen, M Van Wieringen, H Wegdam-den Boer, M E J Zwaveling-Soonawala, N Hokken-Koelega, A C S Producer: 20150806 In: The Journal of clinical endocrinology and metabolism vol. 100 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)