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U Wendel

Showing results (1-10 of 186) with videos related to

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Clinica Chimica Acta; International Journal of Clinical Chemistry|December 22, 1980
Prenatal detection of defects in propionate metabolismU Wendel
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|September 1, 1988
[Diagnostic procedures in pediatric hypoglycemias]U Wendel
Pediatric Research|February 1, 1989
Abnormality of odd-numbered long-chain fatty acids in erythrocyte membrane lipids from patients with disorders of propionate metabolismU Wendel
European Journal of Pediatrics|August 1, 1997
Metabolism of branched-chain amino acids in maple syrup urine diseaseP Schadewaldt, U Wendel
Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz|November 21, 2007
[Rare metabolic diseases]U Wendel, P Burgard
Pediatric Research|November 1, 1987
Comparison of the catabolism of branched-chain L-amino acids in cultured human skin fibroblastsP Schadewaldt, U Wendel
Biochemical Medicine|June 1, 1984
Intracellular levels and metabolism of leucine and alpha-ketoisocaproate in normal and maple syrup urine disease fibroblastsU Wendel, U Langenbeck
Lancet (London, England)|January 20, 1979
Antenatal diagnosis of maple-syrup-urine diseaseU Wendel, U Claussen
European Journal of Pediatrics|July 1, 1996
Towards self-monitoring and self-treatment in phenylketonuria--a way to better diet complianceU Wendel, U Langenbeck
Biochemical Medicine and Metabolic Biology|April 1, 1989
Functional differences in the catabolism of branched-chain L-amino acids in cultured normal and maple syrup urine disease fibroblastsP Schadewaldt, U Wendel
Pageof 19

Showing results (1-10 of 186) with videos related to

Sort By:
Pageof 19
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 22, 1980
Prenatal detection of defects in propionate metabolismU Wendel
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|September 1, 1988
[Diagnostic procedures in pediatric hypoglycemias]U Wendel
Pediatric Research|February 1, 1989
Abnormality of odd-numbered long-chain fatty acids in erythrocyte membrane lipids from patients with disorders of propionate metabolismU Wendel
European Journal of Pediatrics|August 1, 1997
Metabolism of branched-chain amino acids in maple syrup urine diseaseP Schadewaldt, U Wendel
Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz|November 21, 2007
[Rare metabolic diseases]U Wendel, P Burgard
Pediatric Research|November 1, 1987
Comparison of the catabolism of branched-chain L-amino acids in cultured human skin fibroblastsP Schadewaldt, U Wendel
Biochemical Medicine|June 1, 1984
Intracellular levels and metabolism of leucine and alpha-ketoisocaproate in normal and maple syrup urine disease fibroblastsU Wendel, U Langenbeck
Lancet (London, England)|January 20, 1979
Antenatal diagnosis of maple-syrup-urine diseaseU Wendel, U Claussen
European Journal of Pediatrics|July 1, 1996
Towards self-monitoring and self-treatment in phenylketonuria--a way to better diet complianceU Wendel, U Langenbeck
Biochemical Medicine and Metabolic Biology|April 1, 1989
Functional differences in the catabolism of branched-chain L-amino acids in cultured normal and maple syrup urine disease fibroblastsP Schadewaldt, U Wendel
Pageof 19