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Browsing by Author Hayek, J.
Showing results 2 to 5 of 5
| Full Text | Issue Date | Title | Author(s) | | 2011 | Creatine transporter defect diagnosed by proton NMR spectroscopy in males with intellectual disability | Mencarelli, M.A.; Tassini, M.; Pollazzon, M., et al |
| 2012 | Expanding the phenotype associated with FOXG1 mutations and in vivo FoxG1 chromatin-binding dynamics | De Filippis, R.; Pancrazi, L.; Bjorgo, K., et al |
| 2009 | Guanidinoacetate methyltransferase (GAMT) deficiency diagnosed by proton NMR spectroscopy of body fluids. | Engelke, U.F.H.; Tassini, M.; Hayek, J., et al |
| 2010 | Silent increase of urinary ethylmalonic acid is an indicator of nonspecific brain dysfunction. | Zannolli, R.; Buoni, S.; Tassini, M., et al |
Showing results 2 to 5 of 5
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