PHENYLALANINE-HYDROXYLASE ACTIVITY IN HYPERPHENYLALANINÆMIA

A NEW GENETIC ABNORMALITY RESULTING IN GALACTOSE-1-PHOSPHATE URIDYLTRANSFERASE DEFICIENCY

Ernest Beutler, MaryellenC. Baluda, Phillip Sturgeon et al. · The Lancet · 1965 · 118 citations

Life Sciences, Genetics, Molecular Genetics +10

On the Nature of Enzymatic Defect in Phenylpyruvic Oligophrenia

C. Mitoma, R. M. Auld, Sidney Udenfriend · Experimental Biology and Medicine · 1957 · 94 citations

Life Sciences, Biochemistry, Endocrinology +11

Phenylalanine Hydroxylation Cofactor in Phenylketonuria

Seymour Kaufman · Science · 1958 · 90 citations

Life Sciences, Biochemistry, Enzymology +14

Studies on Conversion of Phenylalanine to Tyrosine in Phenylpyruvic Oligophrenia.

Herbert W. Wallace, Kivie Moldave, A Meister · Experimental Biology and Medicine · 1957 · 85 citations

Life Sciences, Biochemistry, Drug Metabolism +12

Argininosuccinic aciduria

Hugo W. Moser, Mary L. Efron, Henry Brow et al. · The American Journal of Medicine · 1967 · 62 citations