Carbohydrate-deficient transferrin values in neonatal and umbilical cord blood

Journal of Inherited Metabolic Disease

Volumn 19, Issue 2, 1996, Pages 253-256

  Van Pelt, J ^a,b   Barker, J A ^a   Velmans, M H ^a   Spaapen, L J M ^a  

^a Department of Clinical Chemistry ^*  (Netherlands)

^b KCHL   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

TRANSFERRIN;

ALCOHOL ABUSE; CONFERENCE PAPER; CONGENITAL DISORDER OF GLYCOSYLATION; DIAGNOSTIC VALUE; HUMAN; IMMUNOCHEMISTRY; ISOELECTRIC FOCUSING; NEWBORN; NEWBORN SCREENING; TRANSFERRIN BLOOD LEVEL; UMBILICAL CORD BLOOD;

CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME; FETAL BLOOD; GLYCOSYLATION; HUMANS; INFANT, NEWBORN; TRANSFERRIN;

EID: 0029980548     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF01799443     Document Type: Conference Paper

References (10)

1. Clayton P, Winchester B, DiTomaso E, Young E, Keir G, Rodeck C (1993) Carbohydrate-deficient glycoprotein syndrome: normal glycosylation in the fetus. Lancet 341: 956.
2. de Jong G, van Eijk HG (1989) Functional properties of the carbohydrate moiety of human transferrin. Int J Biochem 21: 253-263.
3. de Jong G, van Noort WL, Feelders RA, Jeu-Jaspers CMH, van Eijk HG (1992) Adaptation of transferrin protein and glycan synthesis. Clin Chim Acta 212: 27-45.
4. Jaeken J, Carchon H, Stibler H (1993) The carbohydrate-deficient glycoprotein syndromes: pre-Golgi and Golgi disorders? Glycobiology 3: 423-428.
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7. Stibler H, Cederberg B (1993) Diagnosis of the carbohydrate-deficient glycoprotein syndrome by analysis of transferrin in filter paper blood spots. Acta Paediatr 82: 55-59.
8. Stibler H, Kristiansson B (1991) Analysis of transferrin and α-fetoprotein in amniotic fluid and neonatal serum: a possible means for indirect prenatal diagnosis of the carbohydrate-deficient glycoprotein syndrome. Acta Pediatr Scand Suppl 375: 32-38.
9. Stibler H, Jaeken J, Kristiansson B (1991) Biochemical characteristics and diagnosis of the carbohydrate-deficient glycoprotein syndrome. Acta Pediatr Scand Suppl 375: 21-31.
10. van Eijk HG, van Noort WL (1992) The analysis of human serum transferrins with the PhastSystem: quantitation of microheterogenity. Electrophoresis 13: 354-358.