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- W2022085785 abstract "1. A 40-fold increase in urinary p-tyramine was observed in a patient with hereditary tyrosinemia as compared to a control population. 2. The excretion of urinary-free p-tyramine was decreased with the restriction of oral phenylalanine and tyrosine in this patient. The pattern of urinary tyrosine and urinary-free p-tyramine was similar during the period of normal protein diet and restricted diet of phenylalanin and tyrosine. 3. The pattern of urinary-free p-tyramine and tyrosine following oral loads of tyrosine and phenylalanine was similar except for a lag period before a tyramine response was observed. 4. The possibility of the patient with hereditary tyrosinemia providing a model to study the origin of urinary p-tyramine is discussed." @default.
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- W2022085785 date "1977-01-01" @default.
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- W2022085785 title "Urinary p-tyramine in hereditary tyrosinemia: I levels as compared to normal individuals, effect of diet, and relationship to urinary tyrosine" @default.
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- W2022085785 doi "https://doi.org/10.1016/s0009-9120(77)90348-4" @default.
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