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Journal of Inherited Metabolic Disease|February 22, 2000
Psychiatric symptoms of inherited metabolic diseaseY Estrov, F Scaglia, O A BodamerAmerican Journal of Medical Genetics|April 5, 2000
Deletion (9) (p13.1 p21.1)F Scaglia, O A Bodamer, S A Berend, et al.Journal of Child Neurology|April 9, 2001
Mitochondrial DNA depletion associated with partial complex II and IV deficiencies and 3-methylglutaconic aciduriaF Scaglia, V R Sutton, O A Bodamer, et al.European Journal of Pediatrics|August 1, 1997
Measurement of glucose turnover--implications for the study of inborn errors of metabolismD Halliday, O A BodamerJournal of Inherited Metabolic Disease|April 9, 2008
Congenital disorders of glycosylation--a challenging group of IEMsJ Vodopiutz, O A BodamerEuropean Journal of Pediatrics|August 1, 1997
Stable isotope studies in inborn errors of metabolism--implications and conclusionsJ V Leonard, O A BodamerNeurology|September 12, 2000
The effects of l-alanine supplementation in late-onset glycogen storage disease type IIO A Bodamer, D Halliday, J V LeonardEuropean Journal of Pediatrics|August 1, 1997
Dietary treatment in late-onset acid maltase deficiencyO A Bodamer, J V Leonard, D HallidayJournal of Inherited Metabolic Disease|October 27, 2004
Nuclear magnetic resonance spectroscopy in glutaryl-CoA dehydrogenase deficiencyO A Bodamer, S Gruber, S Stöckler-IpsirogluAmerican Journal of Medical Genetics|April 12, 2001
Atypical presentation of amniotic band sequenceO A Bodamer, E J Popek, C BacinoPageof 6