Pinto, AAdams, SAhring, KAllen, HAlmeida, MFGarcia-Arenas, DArslan, NAssoun, MAtik Altınok, YBarrio-Carreras, DBelanger Quintana, ABernabei, SMBontemps, CBoyle, FBruni, GBueno-Delgado, MCaine, GCarvalho, RChrobot, AChyż, KCochrane, BCorreia, CCorthouts, KDaly, ADe Leo, SDesloovere, ADe Meyer, ADe Theux, ADidycz, BDijsselhof, MEDokoupil, KDrabik, JDunlop, CEberle-Pelloth, WEftring, KEkengren, JErrekalde, IEvans, SFoucart, AFokkema, LFrançois, LFrench, MForssell, EGingell, CGonçalves, CGökmen Özel, HGrimsley, AGugelmo, GGyüre, EHeller, CHensler, RJardim, IJoost, CJörg-Streller, MJouault, CJung, AKanthe, MKoç, NKok, I LKozanoğlu, TKumru, BLang, FLang, KLiegeois, ILiguori, ALilje, RĻubina, OManta-Vogli, PMayr, DMeneses, CNewby, CMeyer, UMexia, SNicol, COch, UOlivas, SMPedrón-Giner, CPereira, RPlutowska-Hoffmann, KPurves, JRe Dionigi, AReinson, KRobert, MRobertson, LRocha, JCRohde, CRosenbaum-Fabian, SRossi, ARuiz, MSaligova, JGutiérrez-Sánchez, ASchlune, ASchulpis, KSerrano-Nieto, JSkarpalezou, ASkeath, RSlabbert, AStraczek, KGiżewska, MTerry, AThom, RTooke, ATuokkola, Jvan Dam, Evan den Hurk, TMvan der Ploeg, ECVande Kerckhove, KVan Driessche, Mvan Wegberg, AJvan Wyk, KVasconcelos, CVelez García, VWildgoose, JWinkler, TŻółkowska, JZuvadelli, JMacDonald, A2018-08-292018-08-292018-09Mol Genet Metab Rep. 2018 Aug 8;16:82-89http://hdl.handle.net/10400.17/3049In infants with phenylketonuria (PKU), dietary management is based on lowering and titrating phenylalanine (Phe) intake from breast milk or standard infant formula in combination with a Phe-free infant formula in order to maintain blood Phe levels within target range. Professionals use different methods to feed infants with PKU and our survey aimed to document practices across Europe.engBreastfeedingInherited Metabolic DisordersPKU, PhenylketonuriaPhe, PhenylalaninePhe-Free Infant FormulaPhenylalaninePhenylketonuriaInfant PracticesHDE PEDjournal article10.1016/j.ymgmr.2018.07.008