Use of serum on Guthrie cards in screening for congenital disorders of glycosylation [9]

Clinical Chemistry

Volumn 52, Issue 4, 2006, Pages 774-775

  Carchon, Hubert A ^a,c   Ndosimao, Célestin Nsibu ^b   Van Aerschot, Sandra ^a   Jaeken, Jaak ^a  

^a UNIVERSITY OF LEUVEN   (Belgium)

^b UNIVERSITY OF KINSHASA   (Congo)

^c UNIVERSITY HOSPITALS LEUVEN   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN;

BLOOD SAMPLING; CAPILLARY ELECTROPHORESIS; CLINICAL LABORATORY; CONGENITAL DISORDER; CONGENITAL DISORDER OF GLYCOSYLATION; CONTROLLED STUDY; GLYCOSYLATION; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; ISOELECTRIC FOCUSING; LETTER; MAJOR CLINICAL STUDY; SCREENING TEST; SERUM;

BLOOD SPECIMEN COLLECTION; CARBOHYDRATE METABOLISM, INBORN ERRORS; GLYCOSYLATION; HUMANS; INFANT, NEWBORN; NEONATAL SCREENING; SERUM; TRANSFERRIN;

EID: 33645459043     PISSN: 00099147     EISSN: None     Source Type: Journal    
DOI: 10.1373/clinchem.2005.063305     Document Type: Letter

References (5)

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 Acta 1984;144:245-7.
2. Helander A, Bergström J, Freeze HH. Testing for congenital disorders of glycosylation by HPLC measurement of serum transferrin glycoforms. Clin Chem 2004;50:954-8.
3. Carchon HA, Chevigné R, Falmagne JB, Jaeken J. Diagnosis of congenital disorders of glycosylation by capillary zone electrophoresis of serum transferrin. Clin Chem 2004;50:101-11.
4. Stibler H, Cederberg B. Diagnosis of the carbohydrate-deficient glycoprotein syndrome by analysis of transferrin in filter paper blood spots. Acta Paediatr 1993;82:55-9.
5. Carchon H, Serrus M, Eggermont E. Digestion of gliadin peptides by intestinal mucosa from control or coeliac children. Digestion 1979;19:1-5.