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U Wendel

Showing results (81-90 of 186) with videos related to

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Zeitschrift Fur Kinderheilkunde|February 11, 1974
Maple syrup urine disease variant: report on an infantP Koepp, C Rybak, H W Rüdiger, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 31, 1994
Simultaneous determination of betaine and N,N-dimethylglycine in urineM D Laryea, R Zass, J Ritgen, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 15, 1988
Analysis of the fatty acid composition of erythrocyte phospholipids by a base catalysed transesterification method--prevention of formation of dimethylacetalsM D Laryea, P Cieslicki, E Diekmann, et al.
Pediatric Research|January 1, 1988
Transamination and oxidative decarboxylation rates of branched-chain 2-oxo acids in cultured human skin fibroblastsP Schadewaldt, W Radeck, H W Hammen, et al.
Clinical Chemistry|September 11, 1998
Simple method for the routine determination of betaine and N,N-dimethylglycine in blood and urineM D Laryea, F Steinhagen, S Pawliczek, et al.
Humangenetik|January 1, 1973
Maple syrup urine disease: rapid prenatal diagnosis by enzyme assayU Wendel, H W Rüdiger, E Passarge, et al.
Hoppe-Seyler'S Zeitschrift Fur Physiologische Chemie|October 1, 1972
[Aspects of metabolic correction in cells with pathologically increased mucopolysaccharide storage]U Wendel, W Wöhler, H W Rüdiger, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Genetic counselling and prenatal diagnosis in disorders of the mitochondrial energy metabolismW Ruitenbeek, U Wendel, B C Hamel, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
On the mechanism of L-alloisoleucine formation: studies on a healthy subject and in fibroblasts from normals and patients with maple syrup urine diseaseP Schadewaldt, H W Hammen, C Dalle-Feste, et al.
Acta Paediatrica (Oslo, Norway : 1992)|January 23, 1999
Diurnal changes in plasma amino acids in maple syrup urine diseaseB Schwahn, U Wendel, P Schadewaldt, et al.
Pageof 19

Showing results (81-90 of 186) with videos related to

Sort By:
Pageof 19
Zeitschrift Fur Kinderheilkunde|February 11, 1974
Maple syrup urine disease variant: report on an infantP Koepp, C Rybak, H W Rüdiger, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 31, 1994
Simultaneous determination of betaine and N,N-dimethylglycine in urineM D Laryea, R Zass, J Ritgen, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 15, 1988
Analysis of the fatty acid composition of erythrocyte phospholipids by a base catalysed transesterification method--prevention of formation of dimethylacetalsM D Laryea, P Cieslicki, E Diekmann, et al.
Pediatric Research|January 1, 1988
Transamination and oxidative decarboxylation rates of branched-chain 2-oxo acids in cultured human skin fibroblastsP Schadewaldt, W Radeck, H W Hammen, et al.
Clinical Chemistry|September 11, 1998
Simple method for the routine determination of betaine and N,N-dimethylglycine in blood and urineM D Laryea, F Steinhagen, S Pawliczek, et al.
Humangenetik|January 1, 1973
Maple syrup urine disease: rapid prenatal diagnosis by enzyme assayU Wendel, H W Rüdiger, E Passarge, et al.
Hoppe-Seyler'S Zeitschrift Fur Physiologische Chemie|October 1, 1972
[Aspects of metabolic correction in cells with pathologically increased mucopolysaccharide storage]U Wendel, W Wöhler, H W Rüdiger, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Genetic counselling and prenatal diagnosis in disorders of the mitochondrial energy metabolismW Ruitenbeek, U Wendel, B C Hamel, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
On the mechanism of L-alloisoleucine formation: studies on a healthy subject and in fibroblasts from normals and patients with maple syrup urine diseaseP Schadewaldt, H W Hammen, C Dalle-Feste, et al.
Acta Paediatrica (Oslo, Norway : 1992)|January 23, 1999
Diurnal changes in plasma amino acids in maple syrup urine diseaseB Schwahn, U Wendel, P Schadewaldt, et al.
Pageof 19