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La Clinica Terapeutica|September 7, 2016
Role of Whole-Body MR with DWIBS in child's BartonellosisE Rossi, A Perrone, D Narese, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 24, 2001
Imaging axonal damage in multiple sclerosis by means of MR spectroscopyN De Stefano, S Narayanan, M Mortilla, et al.
Journal of Neurovirology|June 29, 2000
Proton MR spectroscopy to assess axonal damage in multiple sclerosis and other white matter disordersN De Stefano, S Narayanan, P M Matthews, et al.
Neuroscience Letters|January 3, 1994
Absence of APP713 mutation in Italian and Russian families with schizophreniaM Mortilla, L Amaducci, A Bruni, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 3, 2008
Structural and metabolic brain abnormalities in preclinical cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathyM L Stromillo, M T Dotti, M Battaglini, et al.
Neuroscience Letters|September 14, 1992
A novel but non-pathogenic mutation in exon 4 of the human amyloid precursor protein (APP) geneG Vaula, M Mortilla, R Tupler, et al.
Neurology|July 14, 2004
Neocortical volume decrease in relapsing-remitting MS patients with mild cognitive impairmentM P Amato, M L Bartolozzi, V Zipoli, et al.
Neurology|August 1, 1992
Molecular and prospective phenotypic characterization of a pedigree with familial Alzheimer's disease and a missense mutation in codon 717 of the beta-amyloid precursor protein geneH Karlinsky, G Vaula, J L Haines, et al.
Brain Imaging and Behavior|October 9, 2020
Peak width of skeletonized mean diffusivity (PSMD) and cognitive functions in relapsing-remitting multiple sclerosisC Vinciguerra, A Giorgio, J Zhang, et al.
American Journal of Human Genetics|August 1, 1992
Assessment of amyloid beta-protein precursor gene mutations in a large set of familial and sporadic Alzheimer disease casesR E Tanzi, G Vaula, D M Romano, et al.
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