Vittorio Maglione

Mutations in a Gene Encoding a Novel Protein Containing a Phosphotyrosine-Binding Domain Cause Type 2 Cerebral Cavernous Malformations

Christina L. Liquori, Michel J. Berg, Adrian M. Siegel et al. · The American Journal of Human Genetics · 2003 · 343 citations · Full text

Medicine, Molecular Genetics, Neuroscience +14

Ganglioside GM1 induces phosphorylation of mutant huntingtin and restores normal motor behavior in Huntington disease mice

Alba Di Pardo, Vittorio Maglione, Melanie Alpaugh et al. · Proceedings of the National Academy of Sciences · 2012 · 174 citations · Full text

Life Sciences, Neurology, Neuroscience +17

Impaired Ganglioside Metabolism in Huntington's Disease and Neuroprotective Role of GM1

Vittorio Maglione, Paolo Marchi, Alba Di Pardo et al. · Journal of Neuroscience · 2010 · 144 citations · Full text

Life Sciences, Neurology, Neuroscience +17

Low frequency of PDCD10 mutations in a panel of CCM3 probands: potential for a fourth CCM locus

Christina L. Liquori, Michel J. Berg, Ferdinando Squitieri et al. · Human Mutation · 2005 · 112 citations · Full text

Life Sciences, Genetics, Molecular Genetics +10

Impairment of blood-brain barrier is an early event in R6/2 mouse model of Huntington Disease

Alba Di Pardo, Enrico Amico, Francesco Scalabrì et al. · Scientific Reports · 2017 · 105 citations · Full text

Life Sciences, Neurobiology, Neuroscience +14