Congenital disorders of glycosylation: Have you encountered them?

This publication has 79 references indexed in Scilit:

• Syndrome d'hypoglycosylation des glycoprotéines sériques
  Archives de Pédiatrie, 2000
• Roles for glycosylation of cell surface receptors involved in cellular immune recognition
  Journal of Molecular Biology, 1999
• A Novel Disorder of N-Glycosylation Due to Phosphomannose Isomerase Deficiency
  Biochemical and Biophysical Research Communications, 1998
• Hypoglycosylation of a brain glycoprotein (β-trace protein) in CDG syndromes due to phosphomannomutase deficiency and N-acetylglucosaminyl-transferase II deficiency
  Glycobiology, 1997
• Complex functional and structural coagulation abnormalities in the carbohydrate-deficient glycoprotein syndrome type I
  Blood Coagulation & Fibrinolysis, 1996
• Phosphomannomutase deficiency is a cause of carbohydrate‐deficient glycoprotein syndrome type I
  FEBS Letters, 1995
• Oligosaccharides in vertebrate development
  Seminars in Developmental Biology, 1995
• Carbohydrate-deficient glycoprotein syndrome: electrophoretic study of multiple serum glycoproteins
  Brain & Development, 1995
• Failure to diagnose carbohydrate-deficient glycoprotein syndrome prenatally
  Pediatric Neurology, 1994
• The specific site of tunicamycin inhibition in the formation of dolichol‐bound N‐acetylglucosamine derivatives
  FEBS Letters, 1976