Is unilateral spatial neglect a single phenomenon? S. MaeshimaG. TrumanN. Komai Original communication Pages: 412 - 417
T-cell tumour necrosis factor-α receptor binding in demented patients P. BongioanniMaria Rosaria RomanoMonica Borgna Original communication Pages: 418 - 425
Intrafamilial heterogeneity of movement disorders: Report of three cases in one family A. LossosOren CohenAvinoam Reches Original communication Pages: 426 - 430
The use of percutaneous endoscopic gastrostomy (PEG) feeding tubes in patients with neurological disease J. E. R. BrittonG. LipscombA. C. Young Original communication Pages: 431 - 434
Meningitis due to viridans streptococci in adults R. H. EntingJ. de GansL. Spanjaard Original communication Pages: 435 - 438
The genetics of localization-related symptomatic epilepsy: risk of a family history with seizures in patients who have undergone surgery Rolf DegenHans HolthausenPeter Wolf Original communication Pages: 439 - 445
Dominantly inherited leukodystrophy showing cerebellar deficits and spastic paraparesis: a new entity? T. FukazawaH. SasakiK. Tashiro Original communication Pages: 446 - 449
Human herpes virus 6 and human herpes virus 8 DNA sequences in brains of multiple sclerosis patients, normal adults and children E. MerelliR. BedinG. Franchini Original communication Pages: 450 - 454
Plasticity of the spinal cord contributes to neurological improvement after treatment by cervical decompression H. BabaYasuhisa MaezawaShinichi Imura Original communication Pages: 455 - 460
Upside-down reversal of vision in multiple sclerosis Çig˘dem F. Dog˘uluTülay Kansu Letter to the editors Pages: 461 - 461
Pulsed high-dose dexamethasone treatment of polyneuropathy associated with monoclonal gammopathy N. C. NotermansM. VermeulenJ. H. J. Wokke Letter to the editors Pages: 462 - 463
Nerve biopsy findings in hemizygous and heterozygous patients with Fabry’s disease Keiko ToyookaGérard Said Letter to the editors Pages: 464 - 468
Maternally inherited diabetes and deafness with cerebellar ataxia: a new clinical phenotype associated with the mitochondrial DNA 3243 mutation M. AraiShin-ichi Ohshima Letter to the editors Pages: 468 - 469
Delayed-onset hemidystonia secondary to herpes zoster ophthalmicus-related intracerebral arteritis in an adolescent P. BurbaudJ. BergeB. Bioulac Letter to the editors Pages: 470 - 472