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Browsing by Author Hayek, J.

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Full TextIssue DateTitleAuthor(s)
2011Creatine transporter defect diagnosed by proton NMR spectroscopy in males with intellectual disabilityMencarelli, M.A.; Tassini, M.; Pollazzon, M., et al
2012Expanding the phenotype associated with FOXG1 mutations and in vivo FoxG1 chromatin-binding dynamicsDe Filippis, R.; Pancrazi, L.; Bjorgo, K., et al
2009Guanidinoacetate methyltransferase (GAMT) deficiency diagnosed by proton NMR spectroscopy of body fluids.Engelke, U.F.H.; Tassini, M.; Hayek, J., et al
2010Silent 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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