A new Capillary Zone Electrophoresis method for the screening of Congenital Disorders of Glycosylation (CDG)
- 4 January 2010
- journal article
- research article
- Published by Elsevier BV in Clinica Chimica Acta; International Journal of Clinical Chemistry
- Vol. 411 (1-2), 64-66
- https://doi.org/10.1016/j.cca.2009.10.004
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- On the nomenclature of congenital disorders of glycosylation (CDG)Journal of Inherited Metabolic Disease, 2008
- Analytical evaluation of a new capillary electrophoresis method for carbohydrate-deficient transferrin measurementClinica Chimica Acta; International Journal of Clinical Chemistry, 2007
- Congenital Disorders of Glycosylation: CDG-I, CDG-II, and beyond.Current Molecular Medicine, 2007
- Fully automated analysis of Carbohydrate-Deficient Transferrin (CDT) by using a multicapillary electrophoresis systemClinica Chimica Acta; International Journal of Clinical Chemistry, 2007
- Use of Serum on Guthrie Cards in Screening for Congenital Disorders of GlycosylationClinical Chemistry, 2006
- Methods for Detection of Carbohydrate-Deficient Glycoprotein SyndromesSeminars in Pediatric Neurology, 2005
- Diagnosis of Congenital Disorders of Glycosylation by Capillary Zone Electrophoresis of Serum TransferrinClinical Chemistry, 2004
- Automated Serum Protein Electrophoresis by Capillarys®cclm, 2003
- Functional significance of PMM2 mutations in mildly affected patients with congenital disorders of glycosylation IaGenetics in Medicine, 2001
- Approved recommendation (1987) on the theory of reference values. Part 5. Statistical treatment of collected reference values. Determination of reference limitsClinica Chimica Acta; International Journal of Clinical Chemistry, 1987