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In 1960, Robert Guthrie invented a new assay to detect phenylketonuria in newborns, inspiring hope for treating mental… Expand

The data are from 94 children (48 males and 46 females) with PKU born in the period from 1969 to 1987 and treated by the same… Expand

A preterm infant with classic phenylketonuria required rather less than 90 mg/kg of phenylalanine and between 270 and 290 mg/kg… Expand

Information on methods of initiating the phenylalanine-restricted diet was obtained from the medical personnel of sixteen clinics… Expand

Albumaid XP, a phenylalanine-free protein hydrolysate, was used for treatment of five phenylketonuric infants born between… Expand

Six cases of phenylketonuria (PKU) are reported. The patients belong to three different families — three siblings. Genealogic… Expand

Summary The results of dietary treatment of 10 infants and young children with phenylketonuria with a low phenylalanine diet… Expand

Summary The factors to be considered in the selection of children with phenylketonuria for dietary treatment are discussed. It is… Expand

A STUDY was undertaken in 1958 to find a suitable method for obtaining urine specimens from infants during a large scale program… Expand