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Molecular and Cellular Probes|June 17, 1999
Two novel missense mutations causing adrenoleukodystrophy in Italian patientsC Perusi, M Gomez-Lira, M Mottes, et al.Journal of Neuropathology and Experimental Neurology|September 1, 1992
Inherited neuroaxonal dystrophy in C6 deficient rabbitsC Giannini, S Monaco, M Kirschfink, et al.Neuroepidemiology|March 20, 2002
Prevalence of dementia and apolipoprotein e genotype distribution in the elderly of buttapietra, verona province, ItalyM D Benedetti, A Salviati, S Filipponi, et al.Italian Journal of Neurological Sciences|August 1, 1996
Familial cavernous hemangioma with atypical neuroimagingM G Passarin, A Salviati, G Gambina, et al.Neuroscience Letters|July 2, 2016
Mitochondrial DNA haplogroups may influence Fabry disease phenotypeC Simoncini, L Chico, D Concolino, et al.Journal of Neurology|July 29, 2020
Oxidative stress biomarkers in Fabry disease: is there a room for them?C Simoncini, S Torri, V Montano, et al.Journal of Neuropathology and Experimental Neurology|December 6, 2003
Neuropathology of cognitively normal elderlyD S Knopman, J E Parisi, A Salviati, et al.Pageof 3