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Journal of Inherited Metabolic Disease|October 14, 2000
Acylcarnitines in plasma and blood spots of patients with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase defiencyJ L Van Hove, S G Kahler, M D Feezor, et al.Human Molecular Genetics|October 9, 2001
Gestational, pathologic and biochemical differences between very long-chain acyl-CoA dehydrogenase deficiency and long-chain acyl-CoA dehydrogenase deficiency in the mouseK B Cox, D A Hamm, D S Millington, et al.Journal of Inherited Metabolic Disease|February 22, 2000
Acylcarnitines in fibroblasts of patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and other fatty acid oxidation disordersJ J Shen, D Matern, D S Millington, et al.European Journal of Pediatrics|December 22, 1999
Liver transplantation for glycogen storage disease types I, III, and IVD Matern, T E Starzl, W Arnaout, et al.Journal of Inherited Metabolic Disease|December 18, 2008
Essential fatty acid profiling for routine nutritional assessment unmasks adrenoleukodystrophy in an infant with isovaleric acidaemiaR Bonilla Guerrero, L A Wolfe, N Payne, et al.Pediatric Research|August 29, 2000
Glucose-6-phosphatase mutation G188R confers an atypical glycogen storage disease type 1b phenotypeB W Weston, J L Lin, J Muenzer, et al.Pediatric Research|January 3, 2001
Role of common gene variations in the molecular pathogenesis of short-chain acyl-CoA dehydrogenase deficiencyM J Corydon, J Vockley, P Rinaldo, et al.Pediatrics|April 1, 1997
The clinical phenotype of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria): case reports of 23 new patientsK M Gibson, E Christensen, C Jakobs, et al.Pageof 4