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Browsing by Author Monti, L.

Full Text	Issue Date	Title	Author(s)
	2012	Mutations in SLC30A10 cause parkinsonism and dystonia with hypermanganesemia, polycythemia, and chronic liver disease.	Quadri, M.; Federico, A.; Zhao, T.; Breedveld, G.J.; Battisti, C., et al
	2011	Creatine transporter defect diagnosed by proton NMR spectroscopy in males with intellectual disability	Mencarelli, M.A.; Tassini, M.; Pollazzon, M.; Vivi, A.; Calderisi, M., et al
	2010	[(1)H] magnetic resonance spectroscopy of urine: diagnosis of a guanidinoacetate methyl transferase deficiency case.	Tassini, M.; Zannolli, R.; Buoni, S.; Engelke, U.F.H.; Vivi, A., et al