Many patients ask, Can I get this again? (a relapse) and How bad is it? Will I end up in a wheelchair? (severity/progression). These two questions guide this brief review of the clinical spectrum of demyelinating diseases of the central nervous system.

Mitochondrial DNA G8363A mutation in the tRNA Lys gene : clinical features of a new family / R. Virgilio, D. Ronchi, A. Bordoni, E. Fassone, M. Moggio, S. Bonato, G. Conti, C. Donadoni, L. Barbetta, G. Torgano, S. Corti, N. Bresolin, G.P. Comi. - In: JOURNAL OF NEUROLOGY. - ISSN 0340-5354. - 255:Suppl. 2(2008 Jun), pp. 69-69. (Intervento presentato al 18. convegno Meeting of the European Neurological Society tenutosi a Nice nel 2008) [10.1007/s00415-008-6013-y].

Mitochondrial DNA G8363A mutation in the tRNA Lys gene : clinical features of a new family

R. Virgilio
Primo
;
D. Ronchi
Secondo
;
A. Bordoni;E. Fassone;S. Bonato;G. Conti;S. Corti;N. Bresolin
Penultimo
;
G.P. Comi
Ultimo
2008

Abstract

Many patients ask, Can I get this again? (a relapse) and How bad is it? Will I end up in a wheelchair? (severity/progression). These two questions guide this brief review of the clinical spectrum of demyelinating diseases of the central nervous system.
Acute disseminated encephalomyelitis (ADEM); Balo's disease; Chronic relapsing inflammatory optic neuropathy (CRION); Clinically isolated syndromes (CIS); Isolated transverse myelitis (ITM); Marburg's variant; Single isolated optic neuritis (SION)
Settore MED/26 - Neurologia
giu-2008
European Neurological Society
http://www.springerlink.com/content/0340-5354/255/s2/
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/57481
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