Showing results (21-30 of 280) with videos related to
Sort By:
Pageof 28
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|November 1, 1991
[Macrocephaly as the initial manifestation of glutaryl-CoA-dehydrogenase deficiency (glutaric aciduria type I)]F K Trefz, G F Hoffmann, E Mayatepek, et al.Neuropediatrics|October 12, 2005
Neurological manifestations in lysosomal storage disorders - from pathology to first therapeutic possibilitiesB Hoffmann, E MayatepekBiochemical and Biophysical Research Communications|October 3, 1996
Defective degradation of leukotrienes in peroxisomal-deficient human hepatocytesE Mayatepek, B TiepelmannClinica Chimica Acta; International Journal of Clinical Chemistry|September 30, 1993
Increased excretion of endogenous urinary leukotriene E4 in extrahepatic cholestasisE Mayatepek, G PecherClinica Chimica Acta; International Journal of Clinical Chemistry|May 26, 1999
Increased urinary excretion of LTB4 and omega-carboxy-LTB4 in patients with Zellweger syndromeE Mayatepek, B FlockHuman Genetics|November 9, 2000
Mutation analysis in glycogen storage disease type 1 non-aA R Janecke, M Lindner, M Erdel, et al.Klinische Padiatrie|January 25, 2006
[Fabry disease--a provocation for pediatrics]B Hoffmann, E MayatepekActa Paediatrica (Oslo, Norway : 1992)|December 10, 1998
Transient trimethylaminuria in childhoodE Mayatepek, D KohlmüllerLancet (London, England)|November 20, 1998
Leukotriene C4-synthesis deficiency: a new inborn error of metabolism linked to a fatal developmental syndromeE Mayatepek, B FlockJournal of Neuroscience Research|December 18, 2001
3-Ureidopropionate contributes to the neuropathology of 3-ureidopropionase deficiency and severe propionic aciduria: a hypothesisS Kölker, J G Okun, F Hörster, et al.Pageof 28