An introduction to complementary feeding and transitioning to a concentrated second stage protein substitute PKU explore in infants with phenylketonuria.
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This practical guide covers an introduction to complementary foods and transitioning to a concentrated, low volume spoonable protein substitute, PKU explore, in infants diagnosed with phenylketonuria (PKU).
Collaboration with Anita MacDonald
Birmingham Children's Hospital, UK
Reviewed by Maureen Evans
Royal Children's Hospital, Melbourne, Australia
Reviewed by Suzanne Hollander
Los Angeles, USA
Rare disorders of protein metabolism
Glycogen Storage Disease
Paediatric Kidney Disease