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Journal of Inherited Metabolic Disease|December 17, 2008
A data-mining approach to rank candidate protein-binding partners-The case of biogenesis of lysosome-related organelles complex-1 (BLOC-1)I A Rodriguez-Fernandez, E C Dell'Angelica
Journal of Inherited Metabolic Disease|December 17, 2008
Maple syrup urine disease due to a new large deletion at BCKDHA caused by non-homologous recombinationS Quental, E Martins, L Vilarinho, et al.
Journal of Inherited Metabolic Disease|October 7, 2008
Legacies of Garrod's brilliance. One hundred years--and countingL E Rosenberg
Journal of Inherited Metabolic Disease|October 27, 2004
Maternal Phenylketonuria Collaborative Study (MPKUCS)--the 'outliers'W B Hanley, C Azen, R Koch, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Excitotoxicity and bioenergetics in glutaryl-CoA dehydrogenase deficiencyS Kölker, D M Koeller, S Sauer, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Vascular dysfunction as an additional pathomechanism in glutaric aciduria type IC Mühlhausen, S Ergün, K A Strauss, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Correlation of genotype and phenotype in glutaryl-CoA dehydrogenase deficiencyE Christensen, A Ribes, B Merinero, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Maintenance treatment of glutaryl-CoA dehydrogenase deficiencyC Mühlhausen, G F Hoffmann, K A Strauss, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Looking forward--an evidence-based approach to glutaryl-CoA dehydrogenase deficiencyS Kölker, P Burgard, J G Okun, et al.
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