Showing results (181-190 of 280) with videos related to
Sort By:
Pageof 28
Journal of Inherited Metabolic Disease|October 27, 2004
Emergency treatment in glutaryl-CoA dehydrogenase deficiencyS Kölker, C R Greenberg, M Lindner, et al.The Journal of Clinical Investigation|March 1, 1993
Impaired degradation of leukotrienes in patients with peroxisome deficiency disordersE Mayatepek, W D Lehmann, J Fauler, et al.Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|November 1, 2006
Evidence for impaired gluconeogenesis in very long-chain acyl-CoA dehydrogenase-deficient miceU Spiekerkoetter, J Ruiter, C Tokunaga, et al.Anthropologischer Anzeiger; Bericht Uber Die Biologisch-Anthropologische Literatur|February 21, 2012
How much chicken is food? Questioning the definition of food by analyzing amino acid composition of modern convenience productsM Hermanussen, U Gonder, D Stegemann, et al.Journal of Chromatography|May 19, 1993
Use of a thick-film capillary column for the analysis of organic acids in body fluidsW Meier-Augenstein, G F Hoffmann, B Holmes, et al.Klinische Padiatrie|January 1, 1993
[Development of brain atrophy, therapy and therapy monitoring in glutaric aciduria type I (glutaryl-CoA dehydrogenase deficiency)]B Lawrenz-Wolf, K P Herberg, G F Hoffmann, et al.Diabetic Medicine : a Journal of the British Diabetic Association|July 24, 2019
Evaluation of lipoprotein-associated phospholipase A2 as a marker for renal microvasculopathy in adolescents with Type 1 diabetesJ Seyfarth, D Herebian, C Reinauer, et al.Klinische Padiatrie|October 1, 2009
Cat scratch disease--heterogeneous in clinical presentation: five unusual cases of an infection caused by Bartonella henselaeS Weinspach, T Tenenbaum, S Schönberger, et al.Journal of Inherited Metabolic Disease|January 26, 2006
Comprehensive analysis of pyrimidine metabolism in 450 children with unspecific neurological symptoms using high-pressure liquid chromatography-electrospray ionization tandem mass spectrometryC Schmidt, U Hofmann, D Kohlmüller, et al.Journal of Inherited Metabolic Disease|April 9, 2008
Pathogenesis of CNS involvement in disorders of amino and organic acid metabolismS Kölker, S W Sauer, G F Hoffmann, et al.Pageof 28