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G F Hoffmann

Showing results (41-50 of 214) with videos related to

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Journal of Inherited Metabolic Disease|June 29, 1999
3-Hydroxyglutaric and glutaric acids are neurotoxic through NMDA receptors in vitroS Kölker, B Ahlemeyer, J Krieglstein, et al.
Klinische Padiatrie|February 28, 2001
[Hyperthyroidism in early childhood and a very rare variant of glutaric aciduria: coincidence or causal relation?]P Müller, J Buschmann, L Wagner, et al.
Journal of Inherited Metabolic Disease|July 31, 2009
Epilepsy and inborn errors of metabolism in childrenN I Wolf, A García-Cazorla, G F Hoffmann
European Journal of Pediatrics|January 1, 1994
Screening for defects of branched-chain amino acid metabolismK M Gibson, C F Lee, G F Hoffmann
Journal of Neurology|August 27, 1999
Recurrent brain edema in ornithine-transcarbamylase deficiencyS Schwab, S Schwarz, E Mayatepek, et al.
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 22

Showing results (41-50 of 214) with videos related to

Sort By:
Pageof 22
Journal of Inherited Metabolic Disease|June 29, 1999
3-Hydroxyglutaric and glutaric acids are neurotoxic through NMDA receptors in vitroS Kölker, B Ahlemeyer, J Krieglstein, et al.
Klinische Padiatrie|February 28, 2001
[Hyperthyroidism in early childhood and a very rare variant of glutaric aciduria: coincidence or causal relation?]P Müller, J Buschmann, L Wagner, et al.
Journal of Inherited Metabolic Disease|July 31, 2009
Epilepsy and inborn errors of metabolism in childrenN I Wolf, A García-Cazorla, G F Hoffmann
European Journal of Pediatrics|January 1, 1994
Screening for defects of branched-chain amino acid metabolismK M Gibson, C F Lee, G F Hoffmann
Journal of Neurology|August 27, 1999
Recurrent brain edema in ornithine-transcarbamylase deficiencyS Schwab, S Schwarz, E Mayatepek, et al.
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 22