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U Wendel

Showing results (91-100 of 186) with videos related to

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Journal of Inherited Metabolic Disease|October 26, 2006
Variant maple syrup urine disease (MSUD)--the entire spectrumE Simon, N Flaschker, P Schadewaldt, et al.
Scandinavian Journal of Immunology|February 3, 2005
Immunoglobulin isotype profile of tissue transglutaminase autoantibodies is correlated with the clinical presentation of coeliac diseaseJ Schilling, U Spiekerkoetter, U Wohlrab, et al.
Journal of Inherited Metabolic Disease|July 18, 2009
Metabolic phenotypes of phenylketonuria. Kinetic and molecular evaluation of the Blaskovics protein loading testU Langenbeck, P Burgard, U Wendel, et al.
Pediatric Research|May 1, 2001
Whole-body L-leucine oxidation in patients with variant form of maple syrup urine diseaseP Schadewaldt, A Bodner-Leidecker, H W Hammen, et al.
Molecular Genetics and Metabolism|March 23, 2005
Diagnosis of MSUD by newborn screening allows early intervention without extraneous detoxificationK Heldt, B Schwahn, I Marquardt, et al.
Pediatric Research|February 16, 2000
Formation of L-alloisoleucine in vivo: an L-[13C]isoleucine study in manP Schadewaldt, A Bodner-Leidecker, H W Hammen, 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|September 3, 1999
Renal clearance of branched-chain L-amino and 2-oxo acids in maple syrup urine diseaseP Schadewaldt, H W Hammen, A C Ott, et al.
Journal of Inherited Metabolic Disease|February 24, 2001
Branched-chain L-amino acid metabolism in classical maple syrup urine disease after orthotopic liver transplantationA Bodner-Leidecker, U Wendel, J M Saudubray, et al.
Clinical Chemistry|October 3, 1999
Significance of L-alloisoleucine in plasma for diagnosis of maple syrup urine diseaseP Schadewaldt, A Bodner-Leidecker, H W Hammen, et al.
Pageof 19

Showing results (91-100 of 186) with videos related to

Sort By:
Pageof 19
Journal of Inherited Metabolic Disease|October 26, 2006
Variant maple syrup urine disease (MSUD)--the entire spectrumE Simon, N Flaschker, P Schadewaldt, et al.
Scandinavian Journal of Immunology|February 3, 2005
Immunoglobulin isotype profile of tissue transglutaminase autoantibodies is correlated with the clinical presentation of coeliac diseaseJ Schilling, U Spiekerkoetter, U Wohlrab, et al.
Journal of Inherited Metabolic Disease|July 18, 2009
Metabolic phenotypes of phenylketonuria. Kinetic and molecular evaluation of the Blaskovics protein loading testU Langenbeck, P Burgard, U Wendel, et al.
Pediatric Research|May 1, 2001
Whole-body L-leucine oxidation in patients with variant form of maple syrup urine diseaseP Schadewaldt, A Bodner-Leidecker, H W Hammen, et al.
Molecular Genetics and Metabolism|March 23, 2005
Diagnosis of MSUD by newborn screening allows early intervention without extraneous detoxificationK Heldt, B Schwahn, I Marquardt, et al.
Pediatric Research|February 16, 2000
Formation of L-alloisoleucine in vivo: an L-[13C]isoleucine study in manP Schadewaldt, A Bodner-Leidecker, H W Hammen, 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|September 3, 1999
Renal clearance of branched-chain L-amino and 2-oxo acids in maple syrup urine diseaseP Schadewaldt, H W Hammen, A C Ott, et al.
Journal of Inherited Metabolic Disease|February 24, 2001
Branched-chain L-amino acid metabolism in classical maple syrup urine disease after orthotopic liver transplantationA Bodner-Leidecker, U Wendel, J M Saudubray, et al.
Clinical Chemistry|October 3, 1999
Significance of L-alloisoleucine in plasma for diagnosis of maple syrup urine diseaseP Schadewaldt, A Bodner-Leidecker, H W Hammen, et al.
Pageof 19