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U Wendel

Showing results (181-190 of 186) with videos related to

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Pediatric Research|March 27, 2001
Normal clinical outcome in untreated subjects with mild hyperphenylalaninemiaJ Weglage, M Pietsch, R Feldmann, et al.
Journal of Inherited Metabolic Disease|August 1, 1998
Carnitine-acylcarnitine carrier deficiency: identification of the molecular defect in a patientM Huizing, U Wendel, W Ruitenbeek, et al.
Annals of Neurology|June 14, 2000
Clinical and biochemical characteristics of congenital disorder of glycosylation type Ic, the first recognized endoplasmic reticulum defect in N-glycan synthesisS Grünewald, T Imbach, K Huijben, et al.
Journal of Inherited Metabolic Disease|April 29, 2009
Management and outcome in 75 individuals with long-chain fatty acid oxidation defects: results from a workshopU Spiekerkoetter, M Lindner, R Santer, et al.
Journal of Inherited Metabolic Disease|May 20, 2009
Treatment recommendations in long-chain fatty acid oxidation defects: consensus from a workshopU Spiekerkoetter, M Lindner, R Santer, et al.
Journal of Inherited Metabolic Disease|June 20, 2008
Diagnostic work-up and management of patients with isolated methylmalonic acidurias in European metabolic centresT Zwickler, M Lindner, H I Aydin, et al.
Pageof 19

Showing results (181-190 of 186) with videos related to

Sort By:
Pageof 19
You have reached the last page of results.This site can display upto 186 results.
Pediatric Research|March 27, 2001
Normal clinical outcome in untreated subjects with mild hyperphenylalaninemiaJ Weglage, M Pietsch, R Feldmann, et al.
Journal of Inherited Metabolic Disease|August 1, 1998
Carnitine-acylcarnitine carrier deficiency: identification of the molecular defect in a patientM Huizing, U Wendel, W Ruitenbeek, et al.
Annals of Neurology|June 14, 2000
Clinical and biochemical characteristics of congenital disorder of glycosylation type Ic, the first recognized endoplasmic reticulum defect in N-glycan synthesisS Grünewald, T Imbach, K Huijben, et al.
Journal of Inherited Metabolic Disease|April 29, 2009
Management and outcome in 75 individuals with long-chain fatty acid oxidation defects: results from a workshopU Spiekerkoetter, M Lindner, R Santer, et al.
Journal of Inherited Metabolic Disease|May 20, 2009
Treatment recommendations in long-chain fatty acid oxidation defects: consensus from a workshopU Spiekerkoetter, M Lindner, R Santer, et al.
Journal of Inherited Metabolic Disease|June 20, 2008
Diagnostic work-up and management of patients with isolated methylmalonic acidurias in European metabolic centresT Zwickler, M Lindner, H I Aydin, et al.
Pageof 19