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Journal of Inherited Metabolic Disease|June 28, 2006
Normal pregnancy outcome in L-2-hydroxyglutaric aciduriaA Jonckheere, D Carton, J Jaeken, et al.Journal of Inherited Metabolic Disease|April 8, 2006
Successful liver transplantation for argininosuccinate lyase deficiency (ASLD)E Robberecht, S Maesen, A Jonckheere, et al.European Journal of Biochemistry|November 1, 1976
Arginyl-tRNA synthetase from Escherichia coli. Influence of arginine biosynthetic precursors on the charging of arginine-acceptor tRNA with [14C]arginineJ Charlier, E GerloClinical Chemistry|January 24, 1998
Calibration of ion-exchange HPLC measurements of glycohemoglobin: effect on interassay precisionE Gerlo, F GorusEuropean Journal of Biochemistry|September 15, 1975
Identification of NADH-specific and NADPH-specific FMN reductases in Beneckea harveyiE Gerlo, J CharlierBiochemistry|July 10, 1979
Arginyl-tRNA synthetase from Escherichia coli K12. Purification, properties, and sequence of substrate additionJ Charlier, E GerloJournal of Chromatography|September 13, 1985
High-performance liquid chromatographic assay of free norepinephrine, epinephrine, dopamine, vanillylmandelic acid and homovanillic acidE Gerlo, R MalfaitVerhandelingen - 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 JaekenPageof 41