| Autor: |
SHORTLAND, D., SMITH, I., FRANCIS, D. E. M., ERSSER, R., WOLFF, O. H., Francis, D E |
| Zdroj: |
Archives of Disease in Childhood; Mar1985, Vol. 60 Issue 3, p263-265, 3p |
| Abstrakt: |
A preterm infant with classic phenylketonuria required rather less than 90 mg/kg of phenylalanine and between 270 and 290 mg/kg tyrosine daily to achieve a rate of weight gain of around 20 g/kg per day. Using Lofenalac as the low phenylalanine food, the intake of tyrosine, an essential amino acid for patients with phenylketonuria seemed to be limiting in respect of growth. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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