Oliveri RL - Search Results

1

Clinical and genetic study of a large Charcot-Marie-Tooth type 2A family from southern Italy.

Muglia M, Zappia M, Timmerman V, Valentino P, Gabriele AL, Conforti FL, De Jonghe P, Ragno M, Mazzei R, Sabatelli M, Nicoletti G, Patitucci AM, Oliveri RL, Bono F, Gambardella A, Quattrone A. Muglia M, et al. Among authors: oliveri rl. Neurology. 2001 Jan 9;56(1):100-3. doi: 10.1212/wnl.56.1.100. Neurology. 2001. PMID: 11148244

2

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

3

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: oliveri rl. Neurology. 1998 Mar;50(3):799-801. doi: 10.1212/wnl.50.3.799. Neurology. 1998. PMID: 9521281

4

MRI of skeletal muscles in autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths.

Bono F, Gambardella A, Oliveri RL, Aguglia U, Zappia M, Tamburrini O, Quattrone A. Bono F, et al. Among authors: oliveri rl. Eur Neurol. 1998;39(3):191-2. Eur Neurol. 1998. PMID: 9605401 No abstract available.

5

A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chromosome 1.

Gambardella A, Annesi G, De Fusco M, Patrignani A, Aguglia U, Annesi F, Pasqua AA, Spadafora P, Oliveri RL, Valentino P, Zappia M, Ballabio A, Casari G, Quattrone A. Gambardella A, et al. Among authors: oliveri rl. Neurology. 2000 Nov 28;55(10):1467-71. doi: 10.1212/wnl.55.10.1467. Neurology. 2000. PMID: 11094099

6

Pontine lesion of the abducens fasciculus producing so-called posterior internuclear ophthalmoplegia.

Oliveri RL, Bono F, Quattrone A. Oliveri RL, et al. Eur Neurol. 1997;37(1):67-9. doi: 10.1159/000117410. Eur Neurol. 1997. PMID: 9018039 No abstract available.

7

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. Neurology. 1998 Jun;50(6):1833-6. doi: 10.1212/wnl.50.6.1833. Neurology. 1998. PMID: 9633736 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: oliveri rl. 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: oliveri rl. 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: oliveri rl. Ann Neurol. 1998 Nov;44(5):836-9. doi: 10.1002/ana.410440522. Ann Neurol. 1998. PMID: 9818944

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