Ragno M - Search Results

1

Benign monomelic amyotrophy of lower limb: a rare entity with a characteristic muscular CT.

Di Muzio A, Delli Pizzi C, Lugaresi A, Ragno M, Uncini A. Di Muzio A, et al. Among authors: ragno m. J Neurol Sci. 1994 Nov;126(2):153-61. doi: 10.1016/0022-510x(94)90266-6. J Neurol Sci. 1994. PMID: 7853021

2

Acute motor axonal neuropathy with high titer IgG and IgA anti-GD1a antibodies following Campylobacter enteritis.

Lugaresi A, Ragno M, Torrieri F, Di Guglielmo G, Fermani P, Uncini A. Lugaresi A, et al. Among authors: ragno m. J Neurol Sci. 1997 Apr 15;147(2):193-200. doi: 10.1016/s0022-510x(96)05349-x. J Neurol Sci. 1997. PMID: 9106127

3

Lewis-Sumner syndrome in hepatitis C virus infection: a possible pathogenetic association with therapeutic problems.

Caporale CM, Capasso M, Ragno M, Di Muzio A, Uncini A. Caporale CM, et al. Among authors: ragno m. Muscle Nerve. 2006 Jul;34(1):116-21. doi: 10.1002/mus.20517. Muscle Nerve. 2006. PMID: 16453326

4

Possible role for nitric oxide dysregulation in critical illness myopathy.

Capasso M, Di Muzio A, Pandolfi A, Pace M, Di Tomo P, Ragno M, Uncini A. Capasso M, et al. Among authors: ragno m. Muscle Nerve. 2008 Feb;37(2):196-202. doi: 10.1002/mus.20907. Muscle Nerve. 2008. PMID: 17924542

5

Androgen receptor gene (CAG)n repeat analysis in the differential diagnosis between Kennedy disease and other motoneuron disorders.

Ferlini A, Patrosso MC, Guidetti D, Merlini L, Uncini A, Ragno M, Plasmati R, Fini S, Repetto M, Vezzoni P, et al. Ferlini A, et al. Among authors: ragno m. Am J Med Genet. 1995 Jan 2;55(1):105-11. doi: 10.1002/ajmg.1320550125. Am J Med Genet. 1995. PMID: 7702080

6

Wide expressivity variation and high but no gender-related penetrance in two dopa-responsive dystonia families with a novel GCH-I mutation.

Uncini A, De Angelis MV, Di Fulvio P, Ragno M, Annesi G, Filla A, Stuppia L, Gambi D. Uncini A, et al. Among authors: ragno m. Mov Disord. 2004 Oct;19(10):1139-45. doi: 10.1002/mds.20048. Mov Disord. 2004. PMID: 15390021

7

Benign monomelic amyotrophy: description of a patient with a focal motor neuron disorder.

Di Bella P, Logullo F, Tulli D, Ragno M, Scarpelli M. Di Bella P, et al. Among authors: ragno m. Ital J Neurol Sci. 1992 Feb;13(1):84. doi: 10.1007/BF02222894. Ital J Neurol Sci. 1992. PMID: 1559789 No abstract available.

8

Changes in magnetic resonance imaging disease measures over 3 years in mildly disabled patients with relapsing-remitting multiple sclerosis receiving interferon β-1a in the COGnitive Impairment in MUltiple Sclerosis (COGIMUS) study.

Bastianello S, Giugni E, Amato MP, Tola MR, Trojano M, Galletti S, Luccichenti G, Quarantelli M, Picconi O, Patti F; COGIMUS study group. Bastianello S, et al. BMC Neurol. 2011 Oct 14;11:125. doi: 10.1186/1471-2377-11-125. BMC Neurol. 2011. PMID: 21999142 Free PMC article. Clinical Trial.

9

Autosomal dominant cerebellar ataxia type I. Clinical and molecular study in 36 Italian families including a comparison between SCA1 and SCA2 phenotypes.

Filla A, De Michele G, Campanella G, Perretti A, Santoro L, Serlenga L, Ragno M, Calabrese O, Castaldo I, De Joanna G, Cocozza S. Filla A, et al. Among authors: ragno m. J Neurol Sci. 1996 Oct;142(1-2):140-7. doi: 10.1016/0022-510x(96)00177-3. J Neurol Sci. 1996. PMID: 8902734

10

Subcutaneous interferon β-1a may protect against cognitive impairment in patients with relapsing-remitting multiple sclerosis: 5-year follow-up of the COGIMUS study.

Patti F, Morra VB, Amato MP, Trojano M, Bastianello S, Tola MR, Cottone S, Plant A, Picconi O; COGIMUS Study Group. Patti F, et al. PLoS One. 2013 Aug 30;8(8):e74111. doi: 10.1371/journal.pone.0074111. eCollection 2013. PLoS One. 2013. PMID: 24137499 Free PMC article. Clinical Trial.

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