HYDROXYKYNURENINURIA: A CASE OF ABNORMAL TRYPTOPHAN METABOLISM PROBABLY DUE TO A DEFICIENCY OF KYNURENINASE.
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Amino Acid Metabolism, Inborn Errors↗
Biomedical subjects
R G WESTALL
Publications and source records attributed to R G WESTALL.
ARGININOSUCCINIC ACIDURIA. ARGININOSUCCINASE AND ARGINASE IN HUMAN BLOOD CELLS.
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Amino Acid Metabolism, Inborn Errors↗
HOMOCYSTINURIA: A NEW INBORN ERROR OF METABOLISM ASSOCIATED WITH MENTAL DEFICIENCY.
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Amino Acid Metabolism, Inborn Errors↗
DIETARY TREATMENT OF A CHILD WITH MAPLE SYRUP URINE DISEASE (BRANCHED-CHAIN KETOACIDURIA).
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Child↗
Determination of argininosuccinic acid by ion-exchange chromatography.
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Arginine↗
Studies in maple syrup urine disease.
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Child↗
Argininosuccinase activity in brain tissue.
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Arginine↗
Simplified method for detecting formiminoglutamic acid in urine as a test of folic-acid deficiency.
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Folic Acid↗
Argininosuccinic aciduria: identification and reactions of the abnormal metabolite in a newly described form of mental disease, with some preliminary metabolic studies.
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Arginine↗
Maple syrup urine disease: branched-chain keto-aciduria.
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Central Nervous System↗
Maple syrup urine disease.
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Biochemical Phenomena↗
The essential amino acid requirements of infants: valine.
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Biochemical Phenomena↗
Amino acid clearances in cystinuria.
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Amino Acids↗
The plasma amino acids in malnutrition: preliminary observations.
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Amino Acids↗
The partial purification of parathyroid hormone by means of ultrafiltration and displacement chromatography.
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Chromatography↗
Alteration of the duration of action of parathyroid hormone after partial purification.
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Hormones↗
The amino acids and other ampholytes of urine. 3. Unidentified substances excreted in normal human urine.
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Amino Acids↗
The amino acids and other ampholytes of urine. 2. The isolation of a new sulphur-containing amino acid from cat urine.
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Amino Acids↗