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	1.	An atypical course of coxsackievirus A6 associated hand, foot and mouth disease in extremely low birth weight preterm twins. [electronic resource] by Bruning, Andrea H L van der Sanden, Sabine M G ten Hoedt, Amber E Wolthers, Katja C van Kaam, Anton H Pajkrt, Dasja Producer: 20151218 In: Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Parenting a child with phenylketonuria or galactosemia: implications for health-related quality of life. [electronic resource] by ten Hoedt, Amber E Maurice-Stam, Heleen Boelen, Carolien C A Rubio-Gozalbo, M Estela van Spronsen, Francjan J Wijburg, Frits A Bosch, Annet M Grootenhuis, Martha A Producer: 20110715 In: Journal of inherited metabolic disease vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	"MY PKU": increasing self-management in patients with phenylketonuria. A randomized controlled trial. [electronic resource] by Ten Hoedt, Amber E Hollak, Carla Em Boelen, Carolien Ca van der Herberg-van de Wetering, N Ada P Ter Horst, Nienke M Jonkers, Cora F Wijburg, Frits A Bosch, Annet M Producer: 20111018 In: Orphanet journal of rare diseases vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	High phenylalanine levels directly affect mood and sustained attention in adults with phenylketonuria: a randomised, double-blind, placebo-controlled, crossover trial. [electronic resource] by ten Hoedt, Amber E de Sonneville, Leo M J Francois, Baudouin ter Horst, Nienke M Janssen, Mirian C H Rubio-Gozalbo, M Estela Wijburg, Frits A Hollak, Carla E M Bosch, Annet M Producer: 20110512 In: Journal of inherited metabolic disease vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Recessive mutations in EPG5 cause Vici syndrome, a multisystem disorder with defective autophagy. [electronic resource] by Cullup, Thomas Kho, Ay Lin Dionisi-Vici, Carlo Brandmeier, Birgit Smith, Frances Urry, Zoe Simpson, Michael A Yau, Shu Bertini, Enrico McClelland, Verity Al-Owain, Mohammed Koelker, Stefan Koerner, Christian Hoffmann, Georg F Wijburg, Frits A ten Hoedt, Amber E Rogers, R Curtis Manchester, David Miyata, Rie Hayashi, Masaharu Said, Elizabeth Soler, Doriette Kroisel, Peter M Windpassinger, Christian Filloux, Francis M Al-Kaabi, Salwa Hertecant, Jozef Del Campo, Miguel Buk, Stefan Bodi, Istvan Goebel, Hans-Hilmar Sewry, Caroline A Abbs, Stephen Mohammed, Shehla Josifova, Dragana Gautel, Mathias Jungbluth, Heinz Producer: 20130222 In: Nature genetics vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)