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Page 1
Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths: clinical, electrophysiologic, and genetic aspects of a large family.
Quattrone A, Gambardella A, Bono F, Aguglia U, Bolino A, Bruni AC, Montesi MP, Oliveri RL, Sabatelli M, Tamburrini O, Valentino P, Van Broeckhoven C, Zappia M. Quattrone A, et al. Among authors: valentino p. Neurology. 1996 May;46(5):1318-24. doi: 10.1212/wnl.46.5.1318. Neurology. 1996. PMID: 8628474
CAG repeat length and clinical features in three Italian families with spinocerebellar ataxia type 2 (SCA2): early impairment of Wisconsin Card Sorting Test and saccade velocity.
Gambardella A, Annesi G, Bono F, Spadafora P, Valentino P, Pasqua AA, Mazzei R, Montesanti R, Conforti FL, Oliveri RL, Zappia M, Aguglia U, Quattrone A. Gambardella A, et al. Among authors: valentino p. J Neurol. 1998 Oct;245(10):647-52. doi: 10.1007/s004150050261. J Neurol. 1998. PMID: 9776463
Kufs' disease presenting as late-onset epilepsia partialis continua.
Gambardella A, Pasquinelli G, Cittadella R, Bono F, Oliveri RL, Valentino P, Zappia M, Quattrone A, Aguglia U. Gambardella A, et al. Among authors: valentino p. Neurology. 1998 Oct;51(4):1180-2. doi: 10.1212/wnl.51.4.1180. Neurology. 1998. PMID: 9781553
APOE and risk of cognitive impairment in multiple sclerosis.
Oliveri RL, Cittadella R, Sibilia G, Manna I, Valentino P, Gambardella A, Aguglia U, Zappia M, Romeo N, Andreoli V, Bono F, Caracciolo M, Quattrone A. Oliveri RL, et al. Among authors: valentino p. Acta Neurol Scand. 1999 Nov;100(5):290-5. doi: 10.1111/j.1600-0404.1999.tb00398.x. Acta Neurol Scand. 1999. PMID: 10536914
248 results