Messina C - Search Results

1

Diffuse metabolic changes in the brain of patients with familial amyloid polyneuropathy. A proton MRSI study.

Mazzeo A, Toscano A, Stromillo ML, Battaglini M, Messina C, Federico A, Vita G, De Stefano N. Mazzeo A, et al. Among authors: messina c. J Neurol Sci. 2006 Jul 15;246(1-2):31-5. doi: 10.1016/j.jns.2006.01.017. Epub 2006 Mar 10. J Neurol Sci. 2006. PMID: 16530227

2

Immunolocalization and activation of transcription factor nuclear factor kappa B in dysimmune neuropathies and familial amyloidotic polyneuropathy.

Mazzeo A, Aguennouz M, Messina C, Vita G. Mazzeo A, et al. Among authors: messina c. Arch Neurol. 2004 Jul;61(7):1097-102. doi: 10.1001/archneur.61.7.1097. Arch Neurol. 2004. PMID: 15262741

3

Psychosocial impact of presymptomatic genetic testing for transthyretin amyloidotic polyneuropathy.

Graceffa A, Russo M, Vita GL, Toscano A, Dattola R, Messina C, Vita G, Mazzeo A. Graceffa A, et al. Among authors: messina c. Neuromuscul Disord. 2009 Jan;19(1):44-8. doi: 10.1016/j.nmd.2008.09.017. Epub 2008 Dec 11. Neuromuscul Disord. 2009. PMID: 19084401

4

Osteosclerotic myeloma with spinal leptomeningitis and severe polyneuropathy: A case report.

Mazzeo A, Granata F, Vinci S, Musolino C, Nastasi V, Autunno M, Messina C, Vita G, Longo M. Mazzeo A, et al. Among authors: messina c. J Comput Assist Tomogr. 2006 Jul-Aug;30(4):649-52. doi: 10.1097/00004728-200607000-00016. J Comput Assist Tomogr. 2006. PMID: 16845298

5

Expression of cytoskeleton proteins in central core disease.

Vita G, Migliorato A, Baradello A, Mazzeo A, Rodolico C, Falsaperla R, Messina C. Vita G, et al. Among authors: messina c. J Neurol Sci. 1994 Jun;124(1):71-6. doi: 10.1016/0022-510x(94)90013-2. J Neurol Sci. 1994. PMID: 7931424

6

Cardiovascular autonomic dysfunction in multiple sclerosis is likely related to brainstem lesions.

Vita G, Fazio MC, Milone S, Blandino A, Salvi L, Messina C. Vita G, et al. Among authors: messina c. J Neurol Sci. 1993 Dec 1;120(1):82-6. doi: 10.1016/0022-510x(93)90029-x. J Neurol Sci. 1993. PMID: 8289084

7

Cardiovascular autonomic control in Becker muscular dystrophy.

Vita G, Di Leo R, De Gregorio C, Papalia A, Rodolico C, Coglitore S, Messina C. Vita G, et al. Among authors: messina c. J Neurol Sci. 2001 May 1;186(1-2):45-9. doi: 10.1016/s0022-510x(01)00500-7. J Neurol Sci. 2001. PMID: 11412871

8

Is there a relationship between somatic and autonomic neuropathies in chronic alcoholics?

Nicolosi C, Di Leo R, Girlanda P, Messina C, Vita G. Nicolosi C, et al. Among authors: messina c. J Neurol Sci. 2005 Jan 15;228(1):15-9. doi: 10.1016/j.jns.2004.09.024. J Neurol Sci. 2005. PMID: 15607205

9

Clinical and muscle magnetic resonance imaging study of an Italian family with autosomal dominant inclusion body myopathy not linked to known genetic loci.

Rodolico C, Toscano A, Patitucci A, Muglia M, Gaeta M, D'Arrigo G, Migliorato A, Messina S, Quattrone A, Messina C, Vita G. Rodolico C, et al. Among authors: messina s, messina c. Neurol Sci. 2005 Dec;26(5):303-9. doi: 10.1007/s10072-005-0502-x. Neurol Sci. 2005. PMID: 16388363

10

Charcot-Marie-Tooth type X: unusual phenotype of a novel CX32 mutation.

Mazzeo A, Di Leo R, Toscano A, Muglia M, Patitucci A, Messina C, Vita G. Mazzeo A, et al. Among authors: messina c. Eur J Neurol. 2008 Oct;15(10):1140-2. doi: 10.1111/j.1468-1331.2008.02263.x. Epub 2008 Aug 20. Eur J Neurol. 2008. PMID: 18717720

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