Quattrone A - Search Results

1

Cognitive deficits in multiple sclerosis patients with cerebellar symptoms.

Valentino P, Cerasa A, Chiriaco C, Nisticò R, Pirritano D, Gioia M, Lanza P, Canino M, Del Giudice F, Gallo O, Condino F, Torchia G, Quattrone A. Valentino P, et al. Among authors: quattrone a. Mult Scler. 2009 Jul;15(7):854-9. doi: 10.1177/1352458509104589. Mult Scler. 2009. PMID: 19542264

2

Negative myoclonus during valproate-related stupor. Neurophysiological evidence of a cortical non-epileptic origin.

Aguglia U, Gambardella A, Zappia M, Valentino P, Quattrone A. Aguglia U, et al. Among authors: quattrone a. Electroencephalogr Clin Neurophysiol. 1995 Feb;94(2):103-8. doi: 10.1016/0013-4694(94)00268-p. Electroencephalogr Clin Neurophysiol. 1995. PMID: 7532570

3

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. Neurology. 1996 May;46(5):1318-24. doi: 10.1212/wnl.46.5.1318. Neurology. 1996. PMID: 8628474

4

Action palatal tremor in a patient with primary intestinal lymphoma.

Gambardella A, Zappia A, Valentino P, Aguglia U, Fera F, Pardatscher K, Quattrone A. Gambardella A, et al. Among authors: quattrone a. Mov Disord. 1997 Sep;12(5):794-7. doi: 10.1002/mds.870120530. Mov Disord. 1997. PMID: 9380069

5

Genetic heterogeneity in autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths (CMT4B).

Gambardella A, Bolino A, Muglia M, Valentino P, Bono F, Oliveri RL, Sabatelli M, Brancolini V, Van Broeckhoven C, Romeo G, Devoto M, Quattrone A. Gambardella A, et al. Among authors: quattrone a. Neurology. 1998 Mar;50(3):799-801. doi: 10.1212/wnl.50.3.799. Neurology. 1998. PMID: 9521281

6

Randomized trial comparing two different high doses of methylprednisolone in MS: a clinical and MRI study.

Oliveri RL, Valentino P, Russo C, Sibilia G, Aguglia U, Bono F, Fera F, Gambardella A, Zappia M, Pardatscher K, Quattrone A. Oliveri RL, et al. Among authors: quattrone a. Neurology. 1998 Jun;50(6):1833-6. doi: 10.1212/wnl.50.6.1833. Neurology. 1998. PMID: 9633736 Clinical Trial.

7

Pulsed methylprednisolone induces a reversible impairment of memory in patients with relapsing-remitting multiple sclerosis.

Oliveri RL, Sibilia G, Valentino P, Russo C, Romeo N, Quattrone A. Oliveri RL, et al. Among authors: quattrone a. Acta Neurol Scand. 1998 Jun;97(6):366-9. doi: 10.1111/j.1600-0404.1998.tb05967.x. Acta Neurol Scand. 1998. PMID: 9669468 Clinical Trial.

8

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: quattrone a. J Neurol. 1998 Oct;245(10):647-52. doi: 10.1007/s004150050261. J Neurol. 1998. PMID: 9776463

9

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: quattrone a. Neurology. 1998 Oct;51(4):1180-2. doi: 10.1212/wnl.51.4.1180. Neurology. 1998. PMID: 9781553

10

Spinal muscular atrophy due to an isolated deletion of exon 8 of the telomeric survival motor neuron gene.

Gambardella A, Mazzei R, Toscano A, Annesi G, Pasqua A, Annesi F, Quattrone F, Oliveri RL, Valentino P, Bono F, Aguglia U, Zappia M, Vita G, Quattrone A. Gambardella A, et al. Among authors: quattrone f, quattrone a. Ann Neurol. 1998 Nov;44(5):836-9. doi: 10.1002/ana.410440522. Ann Neurol. 1998. PMID: 9818944

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