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Verhandelingen - Koninklijke Academie Voor Geneeskunde Van Belgie|January 1, 1989
[A not-previously described hereditary neurological disease with a deficiency of sialic acid, galactose and N-acetylglucosamine of plasma glycoproteins]J JaekenEuropean Journal of Pediatrics|January 1, 1994
Cerebrospinal fluid as a tool in the diagnosis of neurometabolic diseases: amino acid analysis before and after acid hydrolysisJ JaekenJournal of Inherited Metabolic Disease|August 2, 2003
Komrower Lecture. Congenital disorders of glycosylation (CDG): it's all in it!J JaekenJournal of Inherited Metabolic Disease|July 27, 2004
Congenital disorders of glycosylation (CDG): update and new developmentsJ JaekenVerhandelingen - Koninklijke Academie Voor Geneeskunde Van Belgie|January 1, 1990
[Metabolic diseases: a challenge for pediatrics]J JaekenAnnual Review of Genomics and Human Genetics|November 10, 2001
Congenital disorders of glycosylationJ Jaeken, G MatthijsJournal of Inherited Metabolic Disease|January 1, 1993
The carbohydrate-deficient glycoprotein syndromes: an overviewJ Jaeken, H CarchonAmerican Journal of Medical Genetics|September 5, 1997
Hardikar syndrome: a new syndrome with cleft lip/palate, pigmentary retinopathy and cholestasisF Cools, J JaekenArchives of Disease in Childhood|January 1, 1990
Carbohydrate deficient serum transferrin in a new systemic hereditary syndromeH Stibler, J JaekenPageof 19