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J Zschocke

Showing results (31-40 of 86) with videos related to

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Journal of Inherited Metabolic Disease|March 18, 2003
Emergency management of inherited metabolic diseasesV Prietsch, M Lindner, J Zschocke, et al.
Human Mutation|March 26, 2003
Tetrahydrobiopterin sensitivity in German patients with mild phenylalanine hydroxylase deficiencyM Lindner, R Steinfeld, P Burgard, et al.
Lancet (London, England)|September 15, 1999
Mild trimethylaminuria caused by common variants in FMO3 geneJ Zschocke, D Kohlmueller, E Quak, et al.
Klinische Padiatrie|January 20, 2010
Compliance to clinical guidelines determines outcome in glutaric aciduria type I in the era of newborn screeningI Höliner, B Simma, A Reiter, et al.
Burns : Journal of the International Society for Burn Injuries|October 12, 2000
Eye burns: an emergency and continuing problemN F Schrage, S Langefeld, J Zschocke, et al.
Journal of Inherited Metabolic Disease|September 3, 1999
Large heterozygous deletion masquerading as homozygous missense mutation: a pitfall in diagnostic mutation analysisJ Zschocke, E Quak, A Knauer, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Management of movement disorders in glutaryl-CoA dehydrogenase deficiency: anticholinergic drugs and botulinum toxin as additional therapeutic optionsA P Burlina, G Zara, G F Hoffmann, et al.
Journal of Inherited Metabolic Disease|April 8, 2006
Diagnosis and management of trimethylaminuria (FMO3 deficiency) in childrenR A Chalmers, M D Bain, H Michelakakis, et al.
Human Mutation|January 1, 1994
Non-phenylketonuria hyperphenylalaninaemia in Northern Ireland: frequent mutation allows screening and early diagnosisJ Zschocke, C A Graham, F J Stewart, et al.
Molecular Genetics and Metabolism|March 6, 1999
Glutaryl-CoA dehydrogenase deficiency presenting as 3-hydroxyglutaric aciduriaW L Nyhan, J Zschocke, G Hoffmann, et al.
Pageof 9

Showing results (31-40 of 86) with videos related to

Sort By:
Pageof 9
Journal of Inherited Metabolic Disease|March 18, 2003
Emergency management of inherited metabolic diseasesV Prietsch, M Lindner, J Zschocke, et al.
Human Mutation|March 26, 2003
Tetrahydrobiopterin sensitivity in German patients with mild phenylalanine hydroxylase deficiencyM Lindner, R Steinfeld, P Burgard, et al.
Lancet (London, England)|September 15, 1999
Mild trimethylaminuria caused by common variants in FMO3 geneJ Zschocke, D Kohlmueller, E Quak, et al.
Klinische Padiatrie|January 20, 2010
Compliance to clinical guidelines determines outcome in glutaric aciduria type I in the era of newborn screeningI Höliner, B Simma, A Reiter, et al.
Burns : Journal of the International Society for Burn Injuries|October 12, 2000
Eye burns: an emergency and continuing problemN F Schrage, S Langefeld, J Zschocke, et al.
Journal of Inherited Metabolic Disease|September 3, 1999
Large heterozygous deletion masquerading as homozygous missense mutation: a pitfall in diagnostic mutation analysisJ Zschocke, E Quak, A Knauer, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Management of movement disorders in glutaryl-CoA dehydrogenase deficiency: anticholinergic drugs and botulinum toxin as additional therapeutic optionsA P Burlina, G Zara, G F Hoffmann, et al.
Journal of Inherited Metabolic Disease|April 8, 2006
Diagnosis and management of trimethylaminuria (FMO3 deficiency) in childrenR A Chalmers, M D Bain, H Michelakakis, et al.
Human Mutation|January 1, 1994
Non-phenylketonuria hyperphenylalaninaemia in Northern Ireland: frequent mutation allows screening and early diagnosisJ Zschocke, C A Graham, F J Stewart, et al.
Molecular Genetics and Metabolism|March 6, 1999
Glutaryl-CoA dehydrogenase deficiency presenting as 3-hydroxyglutaric aciduriaW L Nyhan, J Zschocke, G Hoffmann, et al.
Pageof 9