DETERMINATION OF PHENYLALANINE IN BLOOD AND URINE.
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Blood Chemical Analysis↗
Biomedical subjects
L I WOOLF
Publications and source records attributed to L I WOOLF.
GENE EXPRESSION IN HETEROZYGOTES AND SYNTHESIS OF PLASMA ANTIHAEMOPHILIC FACTOR.
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Factor VIII↗
INHERITED METABOLIC DISORDERS: ERRORS OF PHENYLALANINE AND TYROSINE METABOLISM.
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Amino Acid Metabolism, Inborn Errors↗
Gene expression in heterozygotes.
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Chromosomes↗
Nutrition in relation to phenylketonuria.
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Diet↗
A chemical investigation of the defects of myelination in phenylketonuria.
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Brain↗
Recent work on phenylketonuria and maple syrup urine disease (leucinosis).
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Acid-Base Imbalance↗
Atypical phenylketonuria in sisters with normal offspring.
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Family↗
The birthplaces of parents and grandparents of a series of patients with phenylketonuria in in south-east England.
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England↗
Tests for phenylketonuria.
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Body Fluids↗
Hypoglycaemic response to leucine in a leucine-sensitive man.
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Humans↗
The hypoglycaemic effect of leucine and isovaleric acid.
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Blood Glucose↗
Tests for phenylketonuria: results of a one-year programme for its detection in infancy and among mental defectives.
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Humans↗
Maple syrup urine disease; an inborn error of the metabolism of valine, leucine, and isoleucine associated with gross mental deficiency.
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Biochemical Phenomena↗
Idiopathic infantile hypoglycaemia.
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Child↗