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G F Hoffmann

Showing results (141-150 of 214) with videos related to

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Human Genetics|August 2, 2001
Genetic basis of mitochondrial HMG-CoA synthase deficiencyR Aledo, J Zschocke, J Pié, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 29, 2007
Indications for pediatric liver transplantation. Data from the Heidelberg pediatric liver transplantation programG Engelmann, J Schmidt, J Oh, et al.
Journal of the Neurological Sciences|February 13, 2001
Defective metabolism of leukotriene B4 in the Sjögren-Larsson syndromeM A Willemsen, J J Rotteveel, J G de Jong, et al.
Neuropediatrics|October 9, 2002
Aromatic L-amino acid decarboxylase deficiency with hyperdopaminuria. Clinical and laboratory findings in response to different therapiesA Fiumara, C Bräutigam, K Hyland, et al.
BMJ Case Reports|June 21, 2011
Pyridoxal phosphate-dependent neonatal epileptic encephalopathyS Bagci, J Zschocke, G F Hoffmann, et al.
Journal of Inherited Metabolic Disease|August 19, 2007
LC-MS/MS determination of dibasic amino acids for the diagnosis of cystinuria. Application in a family affected by a novel splice-acceptor site mutation in the SLC7A9 geneO Y Al-Dirbashi, K K Abu-Amero, A F Alswaid, et al.
Neurochemistry International|February 17, 2007
Enzymatic and metabolic evidence for a region specific mitochondrial dysfunction in brains of murine succinic semialdehyde dehydrogenase deficiency (Aldh5a1-/- mice)S W Sauer, S Kölker, G F Hoffmann, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|February 26, 2008
Pyridoxal phosphate-dependent neonatal epileptic encephalopathyS Bagci, J Zschocke, G F Hoffmann, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Excitotoxicity and bioenergetics in glutaryl-CoA dehydrogenase deficiencyS Kölker, D M Koeller, S Sauer, et al.
European Journal of Pediatrics|August 1, 1997
Assessment of energy expenditure in metabolic disordersO A Bodamer, G F Hoffmann, G H Visser, et al.
Pageof 22

Showing results (141-150 of 214) with videos related to

Sort By:
Pageof 22
Human Genetics|August 2, 2001
Genetic basis of mitochondrial HMG-CoA synthase deficiencyR Aledo, J Zschocke, J Pié, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 29, 2007
Indications for pediatric liver transplantation. Data from the Heidelberg pediatric liver transplantation programG Engelmann, J Schmidt, J Oh, et al.
Journal of the Neurological Sciences|February 13, 2001
Defective metabolism of leukotriene B4 in the Sjögren-Larsson syndromeM A Willemsen, J J Rotteveel, J G de Jong, et al.
Neuropediatrics|October 9, 2002
Aromatic L-amino acid decarboxylase deficiency with hyperdopaminuria. Clinical and laboratory findings in response to different therapiesA Fiumara, C Bräutigam, K Hyland, et al.
BMJ Case Reports|June 21, 2011
Pyridoxal phosphate-dependent neonatal epileptic encephalopathyS Bagci, J Zschocke, G F Hoffmann, et al.
Journal of Inherited Metabolic Disease|August 19, 2007
LC-MS/MS determination of dibasic amino acids for the diagnosis of cystinuria. Application in a family affected by a novel splice-acceptor site mutation in the SLC7A9 geneO Y Al-Dirbashi, K K Abu-Amero, A F Alswaid, et al.
Neurochemistry International|February 17, 2007
Enzymatic and metabolic evidence for a region specific mitochondrial dysfunction in brains of murine succinic semialdehyde dehydrogenase deficiency (Aldh5a1-/- mice)S W Sauer, S Kölker, G F Hoffmann, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|February 26, 2008
Pyridoxal phosphate-dependent neonatal epileptic encephalopathyS Bagci, J Zschocke, G F Hoffmann, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Excitotoxicity and bioenergetics in glutaryl-CoA dehydrogenase deficiencyS Kölker, D M Koeller, S Sauer, et al.
European Journal of Pediatrics|August 1, 1997
Assessment of energy expenditure in metabolic disordersO A Bodamer, G F Hoffmann, G H Visser, et al.
Pageof 22