Utility of delayed spinal cord injury rehabilitation: an Italian study G. ScivolettoB. MorgantiM. Molinari ORIGINAL Pages: 86 - 90
Validation of the Swedish version of the disease-specific Myasthenia Gravis Questionnaire A. RostedtL. PaduaE. V. Stålberg ORIGINAL Pages: 91 - 96
Two new families with hereditary essential chin myoclonus: clinical features, neurophysiological findings and treatment F. Devetag ChalaupkaF. BartholiniM. Turro ORIGINAL Pages: 97 - 103
Size frequency distributions of the florid prion protein aggregates in variant Creutzfeldt-Jakob disease follow a power-law function R. A. ArmstrongN. J. CairnsJ. W. Ironside ORIGINAL Pages: 104 - 109
Transitory, spontaneously recovering, peripheral facial nerve palsy after vinorelbine administration M. MassiminoF. SimonettiL. Gandola ORIGINAL Pages: 110 - 113
A novel missense mutation in the L1CAM gene in a boy with L1 disease A. SimonatiF. BoarettoM. L. Mostacciuolo CASE REPORT Pages: 114 - 117
Creutzfeldt-Jakob disease presenting as corticobasal degeneration: a neurophysiological study L. AvanzinoL. MarinelliG. Abbruzzese CASE REPORT Pages: 118 - 121
Neurological manifestation of tick-borne encephalitis in North-Eastern Italy B. CruciattiA. BeltrameG. L. Gigli CASE REPORT Pages: 122 - 124
Acute iliopsoas and adductor brevis abscesses presenting with proximal leg muscle weakness F. Devetag Chalaupka CASE REPORT Pages: 125 - 128
Severe amnesia following bilateral medial temporal lobe damage occurring on two distinct occasions G. Di GennaroL. G. GrammaldoA. Picardi CASE REPORT Pages: 129 - 133
Epilepsy and limb girdle muscular dystrophy type 2A: double trouble, serendipitous finding or new phenotype? C. PizzanelliM. MancusoL. Murri CASE REPORT Pages: 134 - 137
SPIR MRI usefulness for steroid treatment management in Tolosa-Hunt syndrome S. ColnaghiA. PichiecchioM. Versino CASE REPORT Pages: 137 - 139
Friedreich’s ataxia: clinical heterogeneity in two sisters M. ArmaniM. ZorteaC. P. Trevisan CASE REPORT Pages: 140 - 142
Clinical and molecular diagnosis of cerebrotendinous xanthomatosis with a review of the mutations in the CYP27A1 gene G. N. GallusM. T. DottiA. Federico UPDATE IN NEUROGENETICS Pages: 143 - 149