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Journal of Inherited Metabolic Disease|August 1, 1998
Regulation of the urea cycle enzyme genes in nitric oxide synthesisM Mori, T Gotoh, A Nagasaki, et al.
Journal of Inherited Metabolic Disease|August 1, 1998
Intragenic complementation at the argininosuccinate lyase locus: reconstruction of the active siteP L Howell, M A Turner, J Christodoulou, et al.
Journal of Inherited Metabolic Disease|August 1, 1998
Liver transplantation for the treatment of urea cycle disordersP F Whitington, E M Alonso, J T Boyle, et al.
Journal of Inherited Metabolic Disease|August 1, 1998
Developing adenoviral-mediated in vivo gene therapy for ornithine transcarbamylase deficiencyS E Raper, J M Wilson, M Yudkoff, et al.
Journal of Inherited Metabolic Disease|August 1, 1998
Evaluation of gene therapy for citrullinaemia using murine and bovine modelsG Patejunas, B Lee, J A Dennis, et al.
Journal of Inherited Metabolic Disease|April 11, 2015
Old treatments for new insights and strategies: proposed management in adults and children with alkaptonuriaJean-Baptiste Arnoux, Kim-Hanh Le Quan Sang, Anais Brassier, et al.
Journal of Inherited Metabolic Disease|April 15, 2015
Vascular endothelial growth factors: multitasking functionality in metabolism, health and diseaseGina A Smith, Gareth W Fearnley, Michael A Harrison, et al.
Journal of Inherited Metabolic Disease|February 6, 2015
Hypervalinemia and hyperleucine-isoleucinemia caused by mutations in the branched-chain-amino-acid aminotransferase geneX L Wang, C J Li, Y Xing, et al.
Journal of Inherited Metabolic Disease|June 14, 2014
Evaluation of an imaging biomarker, Dixon quantitative chemical shift imaging, in Gaucher disease: lessons learnedL van Dussen, E M Akkerman, C E M Hollak, et al.
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