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Protein Substitutes in PKU; Their Historical Evolution.
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Dietary and Biochemical Control of Phenylketonuria.
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The vitamin B12 concentrations of serum and urine of normals and of patients with megaloblastic anaemias and other diseases.
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Megaloblastic anaemia of infancy.
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Megaloblastic anaemia of infancy in Jamaica.
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The phenylalanine requirement of the normal infant.
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The natural history of anaemia associated with protein malnutrition.
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Further experiences in the treatment of phenylketonuria.
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Dietary treatment of an infant with phenylketonuria.
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Megaloblastic anemia in infancy. III. Clinical considerations and analysis.
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Phenylketonuria treated from earliest infancy; report of three cases.
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