1. A specific enzymatic assay for the diagnosis of congenital galactosemia. I. The consumption test;Anderson;J. Lab. Clin. Med,1957
2. The successful treatment of homocystinuria with pyridoxine;Barber;J. Pediat,1969
3. The influence of phenylalanine intake on the chemistry and behavior of a phenylketonuric child;Bickel;Acta Paediat,1954
4. Glycogen storage disease. Observations on the pathologic physiology of two cases of the hepatic form of the disease;Bridge;J. Pediat,1940
5. Further observations of a patient with hyperglycinemia;Childs;Pediatrics,1964