Methods for Detection of Carbohydrate-Deficient Glycoprotein Syndromes
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Pediatrics, Perinatology and Child Health
Reference13 articles.
1. An apparent homozygous X-linked disorder with carbohydrate-deficient serum glycoproteins;Jaeken;Lancet,1987
2. Clinical significance of abnormal heterogeneity of transferrin in relation to alcohol consumption;Stibler;Acta Med Scand,1979
3. Carbohydrate-deficient transferrin and gamma-glutamyltranferase for the detection and monitoring of alcohol use;Anton;Alcohol Clin Exp Res,2002
4. Allelic d variants of transferrin in evaluation of alcohol abuse;Bean;Clin Chem,1994
5. Rapid determination of transferrin isoforms by immunoaffinity liquid chromatography and electrospray mass spectrometry;Lacey;Clin Chem,2001
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1. Solving Glycosylation Disorders: Fundamental Approaches Reveal Complicated Pathways;The American Journal of Human Genetics;2014-02
2. High performance liquid chromatography evaluation of serum carbohydrate-deficient transferrin and more sialylated transferrin glycoforms in children;Scandinavian Journal of Clinical and Laboratory Investigation;2012-02-20
3. The impact of mass spectrometry in the diagnosis of congenital disorders of glycosylation;Journal of Inherited Metabolic Disease;2011-03-08
4. Employment of single-strand conformation polymorphism analysis in screening for α-1,3 glucosyltransferase gene mutation A333V in Croatian population;Journal of Clinical Laboratory Analysis;2011
5. A new Capillary Zone Electrophoresis method for the screening of Congenital Disorders of Glycosylation (CDG);Clinica Chimica Acta;2010-01
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