Development of phenylalanine hydroxylase activity in guinea pig liver.
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Aging↗
Biomedical subjects
H K Berry
Publications and source records attributed to H K Berry.
Cognitive development in early treated phenylketonuria.
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Age Factors↗
Nutritional management in phenylketonuria.
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Amino Acids↗
Uric acid excretion in infants and children.
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Adolescent↗
Amino acid balance in the treatment of phenylketonuria.
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Amino Acids↗
Behavioral abnormalities in rats with neonatal jaundice.
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Analysis of Variance↗
Growth and nutrition in treated phenylketonuric patients.
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Child↗
Histidinemia in two successive generations.
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Adolescent↗
A simple test for histidinuria and histidinemia.
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Amino Acid Metabolism, Inborn Errors↗
Phenylketonuria: intellectual developmental and early treatment.
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Adult↗
Hereditary disorders of amino acid metabolism associated with mental deficiency.
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Amino Acid Metabolism, Inborn Errors↗
A defect in epinephrine synthesis in ascorbic acid-deficient premature infants.
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Ascorbic Acid Deficiency↗
Comparison of fluorimetric and chromatographic procedures for determination of serum phenylalanine.
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Blood Preservation↗
The relation of the ultrastructure of collagen to scar formation and its surgical management.
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Burns↗
Detection of metabolic disorders. Chromatographic procedures and interpretation of results.
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Adolescent↗
Treatment of phenylketonuria.
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Bone Development↗
Conference on treatment of phenylketonuria.
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Diet Therapy↗
The clinical management of phenylketonuria.
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Diet Therapy↗