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U Wendel

Showing results (61-70 of 186) with videos related to

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European Journal of Pediatrics|January 1, 1990
Six-year follow up of phenylalanine intakes and plasma phenylalanine concentrationsU Wendel, K Ullrich, H Schmidt, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Phenylketonuria in Turkey: experience with an enzymatic colorimetric test for measurement of serum phenylalanineU Wendel, I Ozalp, U Langenbeck, et al.
Zeitschrift Fur Ernahrungswissenschaft|December 1, 1990
Age-dependent fatty acid composition of erythrocyte membrane phospholipids in healthy childrenM Laryea, P Cieslicki, E Diekmann, et al.
Analytical Biochemistry|September 20, 1995
Enzymatic method for determination of branched-chain amino acid aminotransferase activityP Schadewaldt, W Hummel, U Wendel, et al.
European Journal of Pediatrics|May 1, 1988
DNA analysis of ornithine transcarbamylase deficiencyU Wendel, E Wilichowski, J Schmidtke, et al.
AJNR. American Journal of Neuroradiology|March 1, 1997
MR and proton MR spectroscopy of the brain in hyperhomocysteinemia caused by methylenetetrahydrofolate reductase deficiencyV Engelbrecht, M Rassek, J Huismann, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Evaluation of prenatal treatment in newborns with cobalamin-responsive methylmalonic acidaemiaR Zass, D Leupold, M A Fernandez, et al.
European Journal of Pediatrics|July 1, 1982
Exchange transfusion in acute episodes of maple syrup urine disease. Studies on branched-chain amino and keto acidsU Wendel, U Langenbeck, I Lombeck, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|August 1, 1985
[Somatostatin in the emergency treatment of persistent hypoglycemias caused by hyperinsulinism (nesidioblastosis of the pancreas)]U Wendel, C Kardorff, P Dorittke, et al.
Journal of Inherited Metabolic Disease|January 14, 1998
Neonatal lethal mitochondrial trifunctional protein deficiency mimicking a respiratory chain defectS Grünewald, J Bakkeren, R A Wanders, et al.
Pageof 19

Showing results (61-70 of 186) with videos related to

Sort By:
Pageof 19
European Journal of Pediatrics|January 1, 1990
Six-year follow up of phenylalanine intakes and plasma phenylalanine concentrationsU Wendel, K Ullrich, H Schmidt, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Phenylketonuria in Turkey: experience with an enzymatic colorimetric test for measurement of serum phenylalanineU Wendel, I Ozalp, U Langenbeck, et al.
Zeitschrift Fur Ernahrungswissenschaft|December 1, 1990
Age-dependent fatty acid composition of erythrocyte membrane phospholipids in healthy childrenM Laryea, P Cieslicki, E Diekmann, et al.
Analytical Biochemistry|September 20, 1995
Enzymatic method for determination of branched-chain amino acid aminotransferase activityP Schadewaldt, W Hummel, U Wendel, et al.
European Journal of Pediatrics|May 1, 1988
DNA analysis of ornithine transcarbamylase deficiencyU Wendel, E Wilichowski, J Schmidtke, et al.
AJNR. American Journal of Neuroradiology|March 1, 1997
MR and proton MR spectroscopy of the brain in hyperhomocysteinemia caused by methylenetetrahydrofolate reductase deficiencyV Engelbrecht, M Rassek, J Huismann, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Evaluation of prenatal treatment in newborns with cobalamin-responsive methylmalonic acidaemiaR Zass, D Leupold, M A Fernandez, et al.
European Journal of Pediatrics|July 1, 1982
Exchange transfusion in acute episodes of maple syrup urine disease. Studies on branched-chain amino and keto acidsU Wendel, U Langenbeck, I Lombeck, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|August 1, 1985
[Somatostatin in the emergency treatment of persistent hypoglycemias caused by hyperinsulinism (nesidioblastosis of the pancreas)]U Wendel, C Kardorff, P Dorittke, et al.
Journal of Inherited Metabolic Disease|January 14, 1998
Neonatal lethal mitochondrial trifunctional protein deficiency mimicking a respiratory chain defectS Grünewald, J Bakkeren, R A Wanders, et al.
Pageof 19