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Journal of Inherited Metabolic Disease|August 2, 2003
Clinical characteristics and diagnostic clues in inborn errors of creatine metabolismC Stromberger, O A Bodamer, S Stöckler-IpsirogluJournal of Inherited Metabolic Disease|July 24, 2007
Expanded newborn screening in Europe 2007O A Bodamer, G F Hoffmann, M LindnerJournal of Paediatrics and Child Health|March 12, 2002
Multiple fractures in a 3-month-old infant with severe infantile osteopetrosisO A Bodamer, R M Bravermann, W J CraigenSeminars in Perinatology|May 20, 1999
Primary and secondary alterations of neonatal carnitine metabolismF Scaglia, N LongoArchives of Disease in Childhood. Fetal and Neonatal Edition|June 29, 2000
Measurement of carbon dioxide production in very low birth weight babiesC C Kingdon, F Mitchell, O A Bodamer, et al.Journal of Inherited Metabolic Disease|January 12, 2008
Comparison of tetrahydrofuran and ethyl acetate as extraction solvents for urinary organic acid analysisGy Wittmann, E Karg, A Mühl, et al.Journal of Child Neurology|July 21, 2007
Severe speech delay as the presenting symptom of guanidinoacetate methyltransferase deficiencyJ Vodopiutz, C B Item, M Häusler, et al.Archives of Biochemistry and Biophysics|March 24, 1999
Functional characterization of the carnitine transporter defective in primary carnitine deficiencyF Scaglia, Y Wang, N LongoAmerican Journal of Physiology. Cell Physiology|March 14, 2001
Insulin increases the turnover rate of Na+-K+-ATPase in human fibroblastsN Longo, F Scaglia, Y WangMolecular Genetics and Metabolism|August 2, 2005
Use of denaturing HPLC to provide efficient detection of mutations causing guanidinoacetate methyltransferase deficiencyC B Item, S Stöckler-Ipsiroglu, C Willheim, et al.Pageof 6