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Browsing by Author Monti, L.
Showing results 1 to 3 of 3
| Full Text | Issue Date | Title | Author(s) | | 2010 | [(1)H] magnetic resonance spectroscopy of urine: diagnosis of a guanidinoacetate methyl transferase deficiency case. | Tassini, M.; Zannolli, R.; Buoni, S., et al |
| 2011 | Creatine transporter defect diagnosed by proton NMR spectroscopy in males with intellectual disability | Mencarelli, M.A.; Tassini, M.; Pollazzon, M., et al |
| 2012 | Mutations in SLC30A10 cause parkinsonism and dystonia with hypermanganesemia, polycythemia, and chronic liver disease. | Quadri, M.; Federico, A.; Zhao, T., et al |
Showing results 1 to 3 of 3
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