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U Wendel

Showing results (71-80 of 186) with videos related to

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Pediatric Research|November 1, 1991
Oral L-alloisoleucine loading studies in healthy subjects and in patients with maple syrup urine diseaseP Schadewaldt, C Dalle-Feste, U Langenbeck, et al.
International Journal for Vitamin and Nutrition Research. Internationale Zeitschrift Fur Vitamin- Und Ernahrungsforschung. Journal International De Vitaminologie Et De Nutrition|January 1, 1989
Plasma tocopherol and tocopherol to lipid ratios in a normal population of infants and childrenM D Laryea, B Biggemann, P Cieslicki, et al.
European Journal of Pediatrics|January 1, 1989
Ornithine transcarbamylase deficiency in a male: strict correlation between metabolic control and plasma arginine concentrationU Wendel, J Wieland, H J Bremer, et al.
European Journal of Pediatrics|December 22, 1999
Liver transplantation in maple syrup urine diseaseU Wendel, J M Saudubray, A Bodner, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Glutaric aciduria mediated by gut bacteriaU Wendel, J Bakkeren, J de Jong, et al.
Deutsche Medizinische Wochenschrift (1946)|January 25, 1974
[Diseases caused by genetic defects in lysosomal muco-polysaccharide-catabolism. Mucopolysaccharidoses]E Passarge, U Wendel, W Wöhler, et al.
Humangenetik|April 24, 1974
Enhancement of amniotic fluid cell growth in cultureH W Rüdiger, R Wolff, U Wendel, et al.
Journal of Inherited Metabolic Disease|May 11, 1999
Novel mutations in patients with fructose-1,6-bisphosphatase deficiencyB Herzog, U Wendel, A A Morris, et al.
Analytical Biochemistry|August 10, 1995
Enzymatic-chemical preparation of quinoxaline derivatives from L-amino acids for gas chromatographic-mass spectrometric analysesP Schadewaldt, H W Hammen, U Wendel, et al.
European Journal of Pediatrics|November 1, 1982
Maple syrup urine disease--therapeutic use of insulin in catabolic statesU Wendel, U Langenbeck, I Lombeck, et al.
Pageof 19

Showing results (71-80 of 186) with videos related to

Sort By:
Pageof 19
Pediatric Research|November 1, 1991
Oral L-alloisoleucine loading studies in healthy subjects and in patients with maple syrup urine diseaseP Schadewaldt, C Dalle-Feste, U Langenbeck, et al.
International Journal for Vitamin and Nutrition Research. Internationale Zeitschrift Fur Vitamin- Und Ernahrungsforschung. Journal International De Vitaminologie Et De Nutrition|January 1, 1989
Plasma tocopherol and tocopherol to lipid ratios in a normal population of infants and childrenM D Laryea, B Biggemann, P Cieslicki, et al.
European Journal of Pediatrics|January 1, 1989
Ornithine transcarbamylase deficiency in a male: strict correlation between metabolic control and plasma arginine concentrationU Wendel, J Wieland, H J Bremer, et al.
European Journal of Pediatrics|December 22, 1999
Liver transplantation in maple syrup urine diseaseU Wendel, J M Saudubray, A Bodner, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Glutaric aciduria mediated by gut bacteriaU Wendel, J Bakkeren, J de Jong, et al.
Deutsche Medizinische Wochenschrift (1946)|January 25, 1974
[Diseases caused by genetic defects in lysosomal muco-polysaccharide-catabolism. Mucopolysaccharidoses]E Passarge, U Wendel, W Wöhler, et al.
Humangenetik|April 24, 1974
Enhancement of amniotic fluid cell growth in cultureH W Rüdiger, R Wolff, U Wendel, et al.
Journal of Inherited Metabolic Disease|May 11, 1999
Novel mutations in patients with fructose-1,6-bisphosphatase deficiencyB Herzog, U Wendel, A A Morris, et al.
Analytical Biochemistry|August 10, 1995
Enzymatic-chemical preparation of quinoxaline derivatives from L-amino acids for gas chromatographic-mass spectrometric analysesP Schadewaldt, H W Hammen, U Wendel, et al.
European Journal of Pediatrics|November 1, 1982
Maple syrup urine disease--therapeutic use of insulin in catabolic statesU Wendel, U Langenbeck, I Lombeck, et al.
Pageof 19