Use of Serum on Guthrie Cards in Screening for Congenital Disorders of Glycosylation
Author:
Affiliation:
1. Department of Pediatrics Center for Metabolic Disease Katholieke Universiteit Leuven Leuven, Belgium
2. Department of Pediatrics University of Kinshasa Kinshasa, Congo
Publisher
Oxford University Press (OUP)
Subject
Biochemistry, medical,Clinical Biochemistry
Link
http://academic.oup.com/clinchem/article-pdf/52/4/774/32686942/clinchem0774.pdf
Reference5 articles.
1. Jaeken J, van Eijk HG, van der Heul C, Corbeel L, Eeckels R, Eggermont E. Sialic acid-deficient serum and cerebrospinal fluid transferrin in a newly recognized genetic syndrome. Clin Chim Acta1984;144:245-247.
2. Helander A, Bergström J, Freeze HH. Testing for congenital disorders of glycosylation by HPLC measurement of serum transferrin glycoforms. Clin Chem2004;50:954-958.
3. Carchon HA, Chevigné R, Falmagne JB, Jaeken J. Diagnosis of congenital disorders of glycosylation by capillary zone electrophoresis of serum transferrin. Clin Chem2004;50:101-111.
4. Stibler H, Cederberg B. Diagnosis of the carbohydrate-deficient glycoprotein syndrome by analysis of transferrin in filter paper blood spots. Acta Paediatr1993;82:55-59.
5. Carchon H, Serrus M, Eggermont E. Digestion of gliadin peptides by intestinal mucosa from control or coeliac children. Digestion1979;19:1-5.
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