Excretion of phenylalanine by normal children and by patients with phenylketonuria
✍ Scribed by Helen K. Berry; Barbara Umbarger; Bettye Livingston
- Book ID
- 118533359
- Publisher
- Elsevier Science
- Year
- 1963
- Tongue
- English
- Weight
- 422 KB
- Volume
- 63
- Category
- Article
- ISSN
- 1097-6833
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
The techniques of systems analysis have been applied to the metabolism of phenylalanine in healthy subjects and in phenylketonuria to derive a computer model. The model consists of seven compartments and four biological functions. Enzyme reactions are assumed to obey Michaelis-Menten kinetics. The c
## Abstract The reproducibility of metabolite content determined by MR spectroscopy (MRS) is usually at best a few percent for the prominent singlets. When studying low‐concentration metabolites, like phenylalanine (Phe), where tissue content can be <100 μmol/kg, better reproducibility is paramount