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J Zschocke

Showing results (21-30 of 86) with videos related to

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Molecular Genetics and Metabolism|May 15, 2001
Tetrahydrobiopterin responsiveness in phenylketonuria differs between patients with the same genotypeM Lindner, D Haas, E Mayatepek, et al.
JIMD Reports|December 20, 2015
Development of Metabolic Phenotype in Phenylketonuria: Evaluation of the Blaskovics Protein Loading Test at 5 Years of AgeP Burgard, E Mönch, J Zschocke, et al.
Journal of Inherited Metabolic Disease|June 29, 1999
Molecular and biochemical basis for variants and deficiency forms of galactose-1-phosphate uridyltransferaseY S Shin, J Zschocke, A M Das, et al.
European Journal of Human Genetics : EJHG|February 5, 1998
A molecular survey of phenylketonuria in Iceland: identification of a founding mutation and evidence of predominant Norse settlementP Guldberg, J Zschocke, A Dagbjartsson, et al.
Neurology|December 11, 2002
Adult onset glutaric aciduria type I presenting with a leukoencephalopathyO Bähr, I Mader, J Zschocke, et al.
Acta Neurologica Scandinavica|March 21, 2002
Leukotrienes in patients with clinically active multiple sclerosisI S Neu, G Metzger, J Zschocke, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|December 1, 1994
The STR system in the human phenylalanine hydroxylase gene: true fragment length obtained with fluorescent labelled PCR primersJ Zschocke, C A Graham, J J McKnight, et al.
American Journal of Human Genetics|December 1, 1995
Phenylketonuria mutation analysis in Northern Ireland: a rapid stepwise approachJ Zschocke, C A Graham, D J Carson, et al.
Human Genetics|August 1, 1997
Phenylketonuria and the peoples of Northern IrelandJ Zschocke, J P Mallory, H G Eiken, et al.
Journal of Inherited Metabolic Disease|June 29, 1999
Biochemistry of glutaric aciduria type I: activities of in vitro expressed wild-type and mutant cDNA encoding human glutaryl-CoA dehydrogenaseM Liesert, J Zschocke, G F Hoffmann, et al.
Pageof 9

Showing results (21-30 of 86) with videos related to

Sort By:
Pageof 9
Molecular Genetics and Metabolism|May 15, 2001
Tetrahydrobiopterin responsiveness in phenylketonuria differs between patients with the same genotypeM Lindner, D Haas, E Mayatepek, et al.
JIMD Reports|December 20, 2015
Development of Metabolic Phenotype in Phenylketonuria: Evaluation of the Blaskovics Protein Loading Test at 5 Years of AgeP Burgard, E Mönch, J Zschocke, et al.
Journal of Inherited Metabolic Disease|June 29, 1999
Molecular and biochemical basis for variants and deficiency forms of galactose-1-phosphate uridyltransferaseY S Shin, J Zschocke, A M Das, et al.
European Journal of Human Genetics : EJHG|February 5, 1998
A molecular survey of phenylketonuria in Iceland: identification of a founding mutation and evidence of predominant Norse settlementP Guldberg, J Zschocke, A Dagbjartsson, et al.
Neurology|December 11, 2002
Adult onset glutaric aciduria type I presenting with a leukoencephalopathyO Bähr, I Mader, J Zschocke, et al.
Acta Neurologica Scandinavica|March 21, 2002
Leukotrienes in patients with clinically active multiple sclerosisI S Neu, G Metzger, J Zschocke, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|December 1, 1994
The STR system in the human phenylalanine hydroxylase gene: true fragment length obtained with fluorescent labelled PCR primersJ Zschocke, C A Graham, J J McKnight, et al.
American Journal of Human Genetics|December 1, 1995
Phenylketonuria mutation analysis in Northern Ireland: a rapid stepwise approachJ Zschocke, C A Graham, D J Carson, et al.
Human Genetics|August 1, 1997
Phenylketonuria and the peoples of Northern IrelandJ Zschocke, J P Mallory, H G Eiken, et al.
Journal of Inherited Metabolic Disease|June 29, 1999
Biochemistry of glutaric aciduria type I: activities of in vitro expressed wild-type and mutant cDNA encoding human glutaryl-CoA dehydrogenaseM Liesert, J Zschocke, G F Hoffmann, et al.
Pageof 9