Discordant CA 19.9 serum results by microparticle enzyme immunoassay and immunoradiometric assay.
نویسندگان
چکیده
References 1. Johnson JL, Wadman SK. Molybdenum cofactor deficiency. In: Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The metabolic basis of inherited disease, 6th ed. New York: McGraw-Hill, 1989:1463-75. 2. Wadman SK, Cats BP, deBree PR Sulfite oxidasedeficiency and the detection of urinary sulfite. Eur J Pediatr 1983;14162-8. 3. Mudd SH, Levy HL, Skovby F. Disorders of transsulfuration. In: Scriver CR, Beaudet AL, Sly WS, Valie D, eds. The metabolic basis of inherited disease, 6th ed. New York: McGraw-Hill, 1989:693-734. 4. Duran M, Aarsen G, Fokkens RH, Nibbering NMM, Cats BP, deBree PK, Wadman SR 2-Mercaptoethanesulfonate-cysteine disulfide excretion following the administration of 2-mercaptoethanesulfonate-a pitfall in the diagnosis of sulfite oxidase deficiency. Clin Chim Acta 1981; 111:47-53.
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ورودعنوان ژورنال:
- Clinical chemistry
دوره 41 7 شماره
صفحات -
تاریخ انتشار 1995