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The Journal of Pediatrics|May 10, 2000
Resting energy expenditure in disorders of propionate metabolismF Feillet, O A Bodamer, M A Dixon, et al.Acta Paediatrica (Oslo, Norway : 1992)|April 30, 2005
Lack of correlation between fatty acid oxidation disorders and haemolysis, elevated liver enzymes, low platelets (HELLP) syndrome?M Holub, O A Bodamer, C Item, et al.European Journal of Pediatrics|August 1, 1997
Protein turnover in critically ill childrenO A Bodamer, J V Leonard, R C Tasker, et al.European Journal of Clinical Nutrition|March 20, 1998
Effects of fish oil supplementation on apolipoprotein B100 production and lipoprotein metabolism in normolipidaemic malesP Bordin, O A Bodamer, S Venkatesan, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|June 20, 2001
Analysis of guanidinoacetate and creatine by isotope dilution electrospray tandem mass spectrometryO A Bodamer, S M Bloesch, A R Gregg, et al.Acta Paediatrica (Oslo, Norway : 1992)|July 4, 2003
Reversibility of cirrhotic regenerative liver nodules upon NTBC treatment in a child with tyrosinaemia type IJ Crone, D Möslinger, O A Bodamer, et al.Journal of Inherited Metabolic Disease|February 1, 2012
Free asymmetric dimethylarginine (ADMA) is low in children and adolescents with classical phenylketonuria (PKU)M Huemer, B Simma, D Mayr, et al.Pediatric Nephrology (Berlin, Germany)|August 25, 1999
Minimal change nephrotic syndrome: a possible complication of ehrlichiosisF Scaglia, L B Vogler, L C Hymes, et al.Gene|July 3, 2013
A novel deletion mutation in the proton-coupled folate transporter (PCFT; SLC46A1) in a Nicaraguan child with hereditary folate malabsorptionN Diop-Bove, M Jain, F Scaglia, et al.Neurology|June 30, 2005
Late-onset neurologic disease in glutaryl-CoA dehydrogenase deficiencyS Külkens, I Harting, S Sauer, et al.Pageof 6