Ausgabe 2/2006
Inhalt (9 Artikel)
Validation of the Swedish version of the disease-specific Myasthenia Gravis Questionnaire
A. Rostedt, L. Padua, E. V. Stålberg
Two new families with hereditary essential chin myoclonus: clinical features, neurophysiological findings and treatment
F. Devetag Chalaupka, F. Bartholini, G. Mandich, M. Turro
Size frequency distributions of the florid prion protein aggregates in variant Creutzfeldt-Jakob disease follow a power-law function
R. A. Armstrong, N. J. Cairns, J. W. Ironside
Creutzfeldt-Jakob disease presenting as corticobasal degeneration: a neurophysiological study
L. Avanzino, L. Marinelli, A. Buccolieri, C. Trompetto, G. Abbruzzese
Severe amnesia following bilateral medial temporal lobe damage occurring on two distinct occasions
G. Di Gennaro, L. G. Grammaldo, P. P. Quarato, V. Esposito, A. Mascia, A. Sparano, G. N. Meldolesi, A. Picardi
Epilepsy and limb girdle muscular dystrophy type 2A: double trouble, serendipitous finding or new phenotype?
C. Pizzanelli, M. Mancuso, R. Galli, A. Choub, M. Fanin, A. C. Nascimbeni, G. Siciliano, L. Murri
SPIR MRI usefulness for steroid treatment management in Tolosa-Hunt syndrome
S. Colnaghi, A. Pichiecchio, S. Bastianello, M. Versino
Friedreich’s ataxia: clinical heterogeneity in two sisters
M. Armani, M. Zortea, E. Pastorello, S. Lombardi, S. Tonello, L. Zuliani, M. T. Rigoni, C. P. Trevisan