Roberto Massa
Department of Neurosciences
Tor Vergata University of Rome
Via Montpellier 1
I-00133
Italy
Name/email consistency: high
- The myotonic dystrophy type 2 (DM2) gene product zinc finger protein 9 (ZNF9) is associated with sarcomeres and normally localized in DM2 patients' muscles. Massa, R., Panico, M.B., Caldarola, S., Fusco, F.R., Sabatelli, P., Terracciano, C., Botta, A., Novelli, G., Bernardi, G., Loreni, F. Neuropathol. Appl. Neurobiol. (2010)
- Late-onset MNGIE without peripheral neuropathy due to incomplete loss of thymidine phosphorylase activity. Massa, R., Tessa, A., Margollicci, M., Micheli, V., Romigi, A., Tozzi, G., Terracciano, C., Piemonte, F., Bernardi, G., Santorelli, F.M. Neuromuscul. Disord. (2009)
- Adult polyglucosan body disease: proton magnetic resonance spectroscopy of the brain and novel mutation in the GBE1 gene. Massa, R., Bruno, C., Martorana, A., de Stefano, N., van Diggelen, O.P., Federico, A. Muscle. Nerve (2008)
- Sural nerve without nerve fibers in leprous neuropathy. Massa, R., Morello, M., Sancesario, G., Bernardi, G. Arch. Neurol. (2002)
- Intracellular localization and isoform expression of the voltage-dependent anion channel (VDAC) in normal and dystrophic skeletal muscle. Massa, R., Marliera, L.N., Martorana, A., Cicconi, S., Pierucci, D., Giacomini, P., De Pinto, V., Castellani, L. J. Muscle Res. Cell. Motil. (2000)
