Messina C - Search Results

1

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: messina c. Eur Neurol. 1995;35(3):177-9. doi: 10.1159/000117120. Eur Neurol. 1995. PMID: 7628502 No abstract available.

2

Multivariate analysis of cardiovascular reflexes applied to the diagnosis of autonomic neuropathy.

Vita G, Princi P, Messina C. Vita G, et al. Among authors: messina c. J Neurol. 1991 Aug;238(5):251-5. doi: 10.1007/BF00319735. J Neurol. 1991. PMID: 1919608

3

Familial oculopharyngeal muscular dystrophy with distal spread.

Vita G, Dattola R, Santoro M, Messina C. Vita G, et al. Among authors: messina c. J Neurol. 1983;230(1):57-64. doi: 10.1007/BF00313597. J Neurol. 1983. PMID: 6194273

4

Bezafibrate-induced myopathy: no evidence for defects in muscle metabolism.

Vita G, Toscano A, Mileto G, Pitrone F, Ferrò MT, Gagliardi E, Bresolin N, Fortunato F, Messina C. Vita G, et al. Among authors: messina c. Eur Neurol. 1993;33(2):168-72. doi: 10.1159/000116927. Eur Neurol. 1993. PMID: 8467827

5

Activation of nuclear factor-kappaB in inflammatory myopathies and Duchenne muscular dystrophy.

Monici MC, Aguennouz M, Mazzeo A, Messina C, Vita G. Monici MC, et al. Among authors: messina c. Neurology. 2003 Mar 25;60(6):993-7. doi: 10.1212/01.wnl.0000049913.27181.51. Neurology. 2003. PMID: 12654966

6

Oromandibular dystonia in a patient with bilateral putaminal necrosis after methanol poisoning: an electrophysiological study.

Quartarone A, Girlanda P, Vita G, Battaglia F, Majorana G, Monici M, Messina C. Quartarone A, et al. Among authors: messina c. Eur Neurol. 2000;44(2):127-8. doi: 10.1159/000008214. Eur Neurol. 2000. PMID: 10965171 No abstract available.

7

Muscle rearrangement in patients with hemiparesis after stroke: an electrophysiological and morphological study.

Dattola R, Girlanda P, Vita G, Santoro M, Roberto ML, Toscano A, Venuto C, Baradello A, Messina C. Dattola R, et al. Among authors: messina c. Eur Neurol. 1993;33(2):109-14. doi: 10.1159/000116915. Eur Neurol. 1993. PMID: 8467816

8

Muscle mitochondria investigation in myotonic dystrophy.

Vita G, Toscano A, Prelle A, Bordoni A, Checcarelli N, Bresolin N, Baradello A, Messina C. Vita G, et al. Among authors: messina c. Eur Neurol. 1993;33(6):423-7. doi: 10.1159/000116987. Eur Neurol. 1993. PMID: 8307063

9

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

10

Muscle phosphoglycerate mutase (PGAM) deficiency in the first Caucasian patient: biochemistry, muscle culture and 31P-MR spectroscopy.

Vita G, Toscano A, Bresolin N, Meola G, Fortunato F, Baradello A, Barbiroli B, Frassineti C, Zaniol P, Messina C. Vita G, et al. Among authors: messina c. J Neurol. 1994 Mar;241(5):289-94. doi: 10.1007/BF00868435. J Neurol. 1994. PMID: 8006681

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