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- W2087606046 abstract "ville, Md.: Department of Health, Education, and Welfare, 1978. (DHEW publication no. (HSA)78-5207). 4. G(athrie R, Susi A. A simple phenylalanine method for detecting phenylketonuria in large populations of newborn infants. Pediatrics 1963;32:338. 5. Levy HL, Waisbren SE. Effects of maternal phenylketonuria and hyperphenylalaninemia on the fetus. N Engl J Med 1983;309:1269. 6. Guthrie R, Murphey WH. Microbiologic screening procedures for detection of errors of metabolism in the newborn infant. In: Bickel H, Hudson FP, Woolf LI, eds. Phenylketonuria and some other errors of amino acid metabolism: biochemistry/genetics/diagnosis/therapy. Stuttgart: George Thieme Verlag, 1971:132-136. 7. Paigen K, Pacholec F, Levy HL. A new method of screening for inherited disorders of galactose metabolism. J Lab Clin Med 1982;99:895. 8. Levy HL, Shih VE, Madigan PM. Routine newborn screening for histidinemia: clinical and biochemical results. N Engl J Med 1'974;291:1214. 9. Guthrie R. Screening for inborn errors of metabglism in the newborn infant: a multiple test program. Bi~:th Defects 1968;4:92. 10. Medical Research Council Steering Committee for the MRC/DHSS Phenylketonuria Register. Routine neonatal screening for phenylketonuria in the United Kingdom 196478. Brit Med J 1981;282:1680. I I. Shih VE, Levy HL, Karoikewicz V, Houghton S, Efron ML, Isselbacher K J, Beutler E, MacCready RA. Galactosemia screening of newborns in Massachusetts. N Engl J Med 197l;284:753. 12. Urbanowski JC, Cohenford MA, Levy HL, Crawford JD, Dain JA. Nonenzymatieally galactosylated serum albumin in a galactosemia infant. N Engl J Med 1982;306:84." @default.
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- W2087606046 title "Intraperitoneal deferoxamine therapy for aluminum intoxication in a child undergoing continuous ambulatory peritoneal dialysis" @default.
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