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Neurology|April 1, 1988
Lack of efficacy of phosphatidylcholine in ataxiasS Sorbi, S Piacentini, P Marini, et al.
Annals of the New York Academy of Sciences|February 15, 2000
Oxidative stress and a key metabolic enzyme in Alzheimer brains, cultured cells, and an animal model of chronic oxidative deficitsG E Gibson, L C Park, H Zhang, et al.
Neuroscience Letters|January 7, 2000
5-HT2A receptor gene polymorphisms in anorexia nervosa and bulimia nervosaB Nacmias, V Ricca, A Tedde, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|October 30, 2003
Interobserver agreement on Poser's and the new McDonald's diagnostic criteria for multiple sclerosisV Zipoli, E Portaccio, G Siracusa, et al.
The Clinical Neuropsychologist|July 9, 2008
A short version of Rao's Brief Repeatable Battery as a screening tool for cognitive impairment in multiple sclerosisE Portaccio, B Goretti, V Zipoli, et al.
Neuroscience Letters|May 4, 2000
Absence of linkage between familial amyotrophic lateral sclerosis and copper chaperone for the superoxide dismutase gene locus in two Italian pedigreesA Orlacchio, T Kawarai, A M Massaro, et al.
Journal of Neural Transmission. Parkinson'S Disease and Dementia Section|January 1, 1990
Changes in pyruvate dehydrogenase complex (PDHc) activity and [3H]QNB-receptor binding in rat brain subsequent to intracerebroventricular injection of bromopyruvateL Frölich, M Strauss, J Kornhuber, et al.
Neuroscience Letters|November 17, 2001
The C677T methylenetetrahydrofolate reductase mutation is not associated with Alzheimer's diseaseT Brunelli, S Bagnoli, B Giusti, et al.
Neuroscience Letters|April 26, 1996
The effect of tetraethylammonium on intracellular calcium concentration in Alzheimer's disease fibroblasts with APP, S182 and E5-1 missense mutationsP Failli, G Tesco, C Ruocco, et al.
Neuroscience Letters|January 31, 1997
Presenilin-1 gene intronic polymorphism in sporadic and familial Alzheimer's diseaseS Sorbi, B Nacmias, A Tedde, et al.
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