Screening for galactosemia.
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Galactosemias↗
Biomedical subjects
V E Shih
Publications and source records attributed to V E Shih.
Homocystinuria associated with decreased methylenetetrahydrofolate reductase activity.
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Adolescent↗
Early dietary management in an infant with argininosuccinase deficiency: preliminary report.
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Ammonia↗
Arginase deficiency in Macaca fascicularis. I. Arginase activity and arginine concentration in erythrocytes and liver.
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Amino Acid Metabolism, Inborn Errors↗
A microassay for argininosuccinase in cultured cells.
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Amino Acid Metabolism, Inborn Errors↗
Massachusetts metabolic disorders screening program. I. Technics and results of urine screening.
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Amino Acid Metabolism, Inborn Errors↗
Persistent mild hyperphenylalaninemia in the untreated state. A prospective study.
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Adolescent↗
Galactosemia screening of newborns in Massachusetts.
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Biological Assay↗
Phenylalanine tolerance tests in simian primates.
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Amino Acid Metabolism, Inborn Errors↗
Studies of intestinal transport defect in Hartnup disease.
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Adolescent↗
Prenatal genetic diagnosis. 3.
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Abortion, Induced↗
Prenatal genetic diagnosis (second of three parts).
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Amino Acid Metabolism, Inborn Errors↗
Pyridoxine-unresponsive homocystinuria.
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Adult↗
Argininosuccinase activity in amniotic-fluid cells.
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Amino Acid Metabolism, Inborn Errors↗
Ornithine-ketoacid transaminase activity in human skin and amniotic fluid cell culture.
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Amino Acid Metabolism, Inborn Errors↗
Epithelial hepatoblastoma associated with congenital hemihypertrophy and cystathioninuria: presentation of a case.
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Amino Acids↗