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Journal of Inherited Metabolic Disease|February 10, 2011
Non-invasive measurements of atherosclerosis in adult cystinosis patientsMartine T P Besouw, Suzanne Holewijn, Elena N Levtchenko, et al.Journal of Inherited Metabolic Disease|February 15, 2011
Brain white matter abnormalities in paediatric Gaucher Type I and Type III using diffusion tensor imagingElin Haf Davies, Kiran K Seunarine, Tina Banks, et al.Journal of Inherited Metabolic Disease|February 25, 2011
Cross-sectional analysis of speech and cognitive performance in 32 patients with classic galactosemiaBjörn Hoffmann, Udo Wendel, Susanne Schweitzer-KrantzJournal of Inherited Metabolic Disease|February 25, 2011
Mild hyperphenylalaninemia: to treat or not to treatFrancjan J van SpronsenJournal of Inherited Metabolic Disease|January 1, 1990
A preliminary report of the collaborative study of maternal phenylketonuria in the United States and CanadaR Koch, W Hanley, H Levy, et al.Journal of Inherited Metabolic Disease|January 1, 1990
Molecular genetics of phosphorylase kinase: cDNA cloning, chromosomal mapping and isoform structureM W KilimannJournal of Inherited Metabolic Disease|January 1, 1990
Cataract and metabolic diseaseW Endres, Y S ShinJournal of Inherited Metabolic Disease|January 1, 1990
Transport of amino acids by the human placenta: predicted effects thereon of maternal hyperphenylalaninaemiaY Kudo, C A BoydJournal of Inherited Metabolic Disease|January 26, 2011
The sodium-dependent di- and tricarboxylate transporter, NaCT, is not responsible for the uptake of D-, L-2-hydroxyglutarate and 3-hydroxyglutarate into neuronsKatja Brauburger, Gerhard Burckhardt, Birgitta C BurckhardtPageof 429