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Human Genetics|June 21, 2001
Molecular and functional characterisation of mild MCAD deficiencyJ Zschocke, A Schulze, M Lindner, et al.Brain Research|October 13, 2001
Intrastriatal administration of 3-hydroxyglutaric acid induces convulsions and striatal lesions in ratsC F de Mello, S Kölker, B Ahlemeyer, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|May 30, 1996
Defective hepatobiliary leukotriene elimination in patients with the Dubin-Johnson syndromeE Mayatepek, W D LehmannArchives of Disease in Childhood|June 1, 1995
Increased generation of cysteinyl leukotrienes in Kawasaki diseaseE Mayatepek, W D LehmannPediatric Research|January 1, 1996
12- and 15-hydroxyeicosatetraenoic acid are excreted in the urine of peroxisome-deficient patients: evidence for peroxisomal metabolism in vivoE Mayatepek, W D LehmannEuropean Journal of Pediatrics|January 1, 1994
Selective screening for inborn errors of metabolism--past, present and futureG F HoffmannEuropean Journal of Pediatrics|November 19, 1997
Persistent hyperinsulinaemic hypoglycaemia of infancy: therapy, clinical outcome and mutational analysisT Meissner, W Brune, E MayatepekClinica Chimica Acta; International Journal of Clinical Chemistry|July 15, 1999
Sensitivity of electrospray-tandem mass spectrometry using the phenylalanine/tyrosine-ratio for differential diagnosis of hyperphenylalaninemia in neonatesA Schulze, D Kohlmueller, E MayatepekMediators of Inflammation|January 1, 1993
Enhanced levels of leukotriene B(4) in synovial fluid in Lyme diseaseE Mayatepek, D Hassler, M MaiwaldThe Journal of Pediatrics|July 11, 2001
Long-term clinical outcome in patients with glutathione synthetase deficiencyE Ristoff, E Mayatepek, A LarssonPageof 28