The genetic mechanism of idiopathic hyperlipemia.
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Cardiovascular Diseases↗
Biomedical subjects
D Y HSIA
Publications and source records attributed to D Y HSIA.
Pregnancy in the diabetic mother with nephritis.
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Diabetes Mellitus↗
A case of phenylketonuria with borderline intelligence.
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Humans↗
The dietary phenylalanine requirements and tolerances of phenylketonuric patients.
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Biochemical Phenomena↗
Pathogenetic problems in phenylketonuria.
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Phenylketonurias↗
Recent developments in the study of hereditary diseases in children.
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Child↗
Birth weight in infants of diabetic mothers.
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Birth Weight↗
The laboratory detection of heterozygotes.
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Genetics↗
Detection of the heterozygous carriers of phenylketonuria.
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Heterozygote↗
Detection by phenylalanine tolerance tests of heterozygous carriers of phenylketonuria.
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Drug Tolerance↗
Gamma globulin in the prevention of infectious hepatitis; studies on the use of small doses in family outbreaks.
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Biomedical Research↗
Coproporphyrin studies in children. I. Urinary coproporphyrin excretion in normal children.
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Body Fluids↗
Coproporphyrin studies in children. 2. Erythrocyte coproporphyrin and protoporphyrin levels in normal infants and children.
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Coproporphyrins↗
Studies of the mechanical fragility of erythrocytes. II. Relation to physiologic jaundice of the newborn infant.
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Erythrocytes↗
Prolonged obstructive jaundice in infancy. IV. Neonatal hepatitis.
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Child↗
Family outbreaks of infectious hepatitis; prophylactic use of gamma globulin.
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Disease Outbreaks↗
Serum bilirubin levels in the newborn infant.
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Bilirubin↗