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S Kölker

Showing results (1-10 of 46) with videos related to

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Journal of Inherited Metabolic Disease|October 27, 2004
Reduction of lysine intake while avoiding malnutrition--major goals and major problems in dietary treatment of glutaryl-CoA dehydrogenase deficiencyE Müller, S Kölker
Neurology|April 23, 2003
Adult onset glutaric aciduria type I presenting with a leukoencephalopathyS Kölker, G F Hoffmann
Cellular and Molecular Life Sciences : CMLS|March 17, 2005
Methylmalonic acid--an endogenous toxin?S Kölker, J G Okun
Neuropediatrics|January 22, 2003
White matter disease in cerebral organic acid disorders: clinical implications and suggested pathomechanismsS Kölker, E Mayatepek, G F Hoffmann
Journal of Inherited Metabolic Disease|April 8, 2006
Acrodermatitis acidaemia secondary to 'overtreatment' and protein deficiencyG F Hoffmann, R Happle, S Kölker
Amino Acids|May 4, 2000
Cerebral organic acid disorders induce neuronal damage via excitotoxic organic acids in vitroS Kölker, B Ahlemeyer, J Krieglstein, et al.
Pediatric Research|June 23, 2001
Contribution of reactive oxygen species to 3-hydroxyglutarate neurotoxicity in primary neuronal cultures from chick embryo telencephalonsS Kölker, B Ahlemeyer, J Krieglstein, et al.
Journal of Inherited Metabolic Disease|July 15, 2000
Methylmalonic acid induces excitotoxic neuronal damage in vitroS Kölker, B Ahlemeyer, J Krieglstein, et al.
Journal of Inherited Metabolic Disease|July 15, 2000
Evaluation of trigger factors of acute encephalopathy in glutaric aciduria type I: fever and tumour necrosis factor-alphaS Kölker, B Ahlemeyer, J Krieglstein, et al.
Pediatric Research|April 12, 2000
Maturation-dependent neurotoxicity of 3-hydroxyglutaric and glutaric acids in vitro: a new pathophysiologic approach to glutaryl-CoA dehydrogenase deficiencyS Kölker, B Ahlemeyer, J Krieglstein, et al.
Pageof 5

Showing results (1-10 of 46) with videos related to

Sort By:
Pageof 5
Journal of Inherited Metabolic Disease|October 27, 2004
Reduction of lysine intake while avoiding malnutrition--major goals and major problems in dietary treatment of glutaryl-CoA dehydrogenase deficiencyE Müller, S Kölker
Neurology|April 23, 2003
Adult onset glutaric aciduria type I presenting with a leukoencephalopathyS Kölker, G F Hoffmann
Cellular and Molecular Life Sciences : CMLS|March 17, 2005
Methylmalonic acid--an endogenous toxin?S Kölker, J G Okun
Neuropediatrics|January 22, 2003
White matter disease in cerebral organic acid disorders: clinical implications and suggested pathomechanismsS Kölker, E Mayatepek, G F Hoffmann
Journal of Inherited Metabolic Disease|April 8, 2006
Acrodermatitis acidaemia secondary to 'overtreatment' and protein deficiencyG F Hoffmann, R Happle, S Kölker
Amino Acids|May 4, 2000
Cerebral organic acid disorders induce neuronal damage via excitotoxic organic acids in vitroS Kölker, B Ahlemeyer, J Krieglstein, et al.
Pediatric Research|June 23, 2001
Contribution of reactive oxygen species to 3-hydroxyglutarate neurotoxicity in primary neuronal cultures from chick embryo telencephalonsS Kölker, B Ahlemeyer, J Krieglstein, et al.
Journal of Inherited Metabolic Disease|July 15, 2000
Methylmalonic acid induces excitotoxic neuronal damage in vitroS Kölker, B Ahlemeyer, J Krieglstein, et al.
Journal of Inherited Metabolic Disease|July 15, 2000
Evaluation of trigger factors of acute encephalopathy in glutaric aciduria type I: fever and tumour necrosis factor-alphaS Kölker, B Ahlemeyer, J Krieglstein, et al.
Pediatric Research|April 12, 2000
Maturation-dependent neurotoxicity of 3-hydroxyglutaric and glutaric acids in vitro: a new pathophysiologic approach to glutaryl-CoA dehydrogenase deficiencyS Kölker, B Ahlemeyer, J Krieglstein, et al.
Pageof 5