Diet in relation to hereditary metabolic disorders.
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Diet↗
Biomedical subjects
D Y HSIA
Publications and source records attributed to D Y HSIA.
Galactosemia: a study of twenty-seven kindreds in North America.
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Galactose↗
Lipoprotein lipase in cystic fibrosis of the pancreas.
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Cystic Fibrosis↗
[Human biochemical genetics].
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Genetics, Medical↗
Clinical management of phenylketonuria.
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Diet↗
Galactosemia: clinical, genetic, and biochemical study.
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Galactose↗
Blood glucose-6-phosphate in heterozygous carriers and patients with liver glycogen disease (Von Gierke's disease).
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Glucose-6-Phosphate↗
Genetic errors of metabolism and environmental interaction: a synthesis.
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Environment↗
A manometric assay for glucose-6-phosphate dehydrogenase.
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Biological Assay↗
Variability in the clinical manifestations of galactosemia.
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Child↗
The metabolism of indole-compounds in phenvlketonuria.
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Biochemical Phenomena↗
The excretion of 5-hydroxyindoleacetic acid in the heterozygous carrier for phenylketonuria.
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Biological Transport↗
Metabolism of 5-hydroxyindole compounds in experimentally produced phenylketonuric rats.
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Animals↗
Clinical course of hyperbilirubinemia in premature infants. A preliminary report.
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Bilirubin↗
Inhibition of glucuronosyl transferase by progestational agents from serum of pregnant women.
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Female↗