The dietary treatment of phenylketonuria.
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Diet↗
Biomedical subjects
L I WOOLF
Publications and source records attributed to L I WOOLF.
The urinary excretion of amino acids and sugars in early infancy.
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Amino Acids↗
The nephrotic syndrome in early infancy: a report of three cases.
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Child↗
Phenylketonuria with normal intelligence and Gowers' muscular dystrophy.
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Humans↗
Urinary excretion of amino-acids and sugar in the nephrotic syndrome; a chromatographic study.
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Amino Acids↗
Familial hypoglycemia precipitated by amino acids.
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Amino Acids↗
Treatment of phenylketonuria with a diet low in phenylalanine.
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Diet↗
The photography of paper chromatograms.
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Chromatography↗
The sugar-containing lipids of Gaucher's disease.
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Cerebrosides↗
Use of ion-exchange resins in paper chromatography of sugars.
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Carbohydrates↗
Estimation of phenylpyruvic acid.
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Humans↗
Specificity and mechanism of the Hunter reaction for ergothioneine.
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Ergothioneine↗
Phenylketonuria with a study of the effect upon it of glutamic acid.
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Glutamates↗
Excretion of conjugated phenylacetic acid in phenylketonuria.
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Biological Transport↗
The determination of ergothioneine; the non-occurrence of ergothioneine in urine.
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Ergothioneine↗
The metabolism of tyrosine and phenylalanine in premature infants; the effect of large doses.
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Humans↗