Bono F - Search Results

1

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

2

Chronic inflammatory demyelinating polyneuropathy in patient with rheumatoid arthritis.

Zappia M, Valentino P, Bono F, Vita G, Aguglia U, Messina C, Quattrone A. Zappia M, et al. Among authors: bono f. Eur Neurol. 1995;35(3):177-9. doi: 10.1159/000117120. Eur Neurol. 1995. PMID: 7628502 No abstract available.

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

4

Localization of a gene responsible for autosomal recessive demyelinating neuropathy with focally folded myelin sheaths to chromosome 11q23 by homozygosity mapping and haplotype sharing.

Bolino A, Brancolini V, Bono F, Bruni A, Gambardella A, Romeo G, Quattrone A, Devoto M. Bolino A, et al. Among authors: bono f. Hum Mol Genet. 1996 Jul;5(7):1051-4. doi: 10.1093/hmg/5.7.1051. Hum Mol Genet. 1996. PMID: 8817346

5

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

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

6

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. Eur Neurol. 1998;39(3):191-2. Eur Neurol. 1998. PMID: 9605401 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. Among authors: bono f. 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: bono f. 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: bono f. 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: bono f. Ann Neurol. 1998 Nov;44(5):836-9. doi: 10.1002/ana.410440522. Ann Neurol. 1998. PMID: 9818944

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