Personal experience with the application of carbohydrate-deficient transferrin (CDT) assays to the detection of congenital disorders of glycosylation

Clinical Chemistry and Laboratory Medicine

Volumn 38, Issue 10, 2000, Pages 965-969

  Colome, C ^a   Ferrer, I ^a   Artuch, R ^a   Vilaseca, M A ^a   Pineda, M ^a   Briones, P ^a  

^a HOSPITAL SANT JOAN DE DÉU   (Spain)

Author keywords

Carbohydrate deficient transferrin; Congenital disorders of glycosylation; Glycoprotein; Inborn error; Sialic acid; Sialotransferrin

Indexed keywords

ALCOHOL; CARBOHYDRATE DEFICIENT TRANSFERRIN; GLYCOPROTEIN; TRANSFERRIN;

ADOLESCENT; ADULT; ALCOHOL BLOOD LEVEL; ALCOHOL CONSUMPTION; ARTICLE; CHILD; CONGENITAL DISORDER OF GLYCOSYLATION; CONTROLLED STUDY; DIAGNOSTIC ACCURACY; DIAGNOSTIC VALUE; DISEASE CLASSIFICATION; FEMALE; GLYCOPROTEIN SYNTHESIS; GLYCOSYLATION; HUMAN; IMMUNOASSAY; INFANT; ISOELECTRIC FOCUSING; MAJOR CLINICAL STUDY; MALE; NEWBORN; POPULATION RESEARCH; POPULATION RISK; PRIORITY JOURNAL; PROTEIN BLOOD LEVEL; RADIOIMMUNOASSAY; RELIABILITY; SCREENING TEST; TURBIDIMETRY;

EID: 0033652951     PISSN: 14346621     EISSN: None     Source Type: Journal    
DOI: 10.1515/CCLM.2000.143     Document Type: Article

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