Issue 7/1997
Content (15 Articles)
Is unilateral spatial neglect a single phenomenon?
S. Maeshima, G. Truman, D. S. Smith, N. Dohi, K. Nakai, T. Itakura, N. Komai
T-cell tumour necrosis factor-α receptor binding in demented patients
P. Bongioanni, Maria Rosaria Romano, Roberto Sposito, Maura Castagna, Barbara Boccardi, Monica Borgna
Intrafamilial heterogeneity of movement disorders: Report of three cases in one family
A. Lossos, Oren Cohen, Vardiella Meiner, Anat Blumenfeld, Avinoam Reches
The use of percutaneous endoscopic gastrostomy (PEG) feeding tubes in patients with neurological disease
J. E. R. Britton, G. Lipscomb, P. D. Mohr, W. D. Rees, A. C. Young
Meningitis due to viridans streptococci in adults
R. H. Enting, J. de Gans, J. P. Blankevoort, L. Spanjaard
The genetics of localization-related symptomatic epilepsy: risk of a family history with seizures in patients who have undergone surgery
Rolf Degen, Hans Holthausen, Peter Wolf
Dominantly inherited leukodystrophy showing cerebellar deficits and spastic paraparesis: a new entity?
T. Fukazawa, H. Sasaki, S. Kikuchi, K. Hamada, T. Hamada, K. Tashiro
Human herpes virus 6 and human herpes virus 8 DNA sequences in brains of multiple sclerosis patients, normal adults and children
E. Merelli, R. Bedin, P. Sola, P. Barozzi, G. L. Mancardi, G. Ficarra, G. Franchini
Plasticity of the spinal cord contributes to neurological improvement after treatment by cervical decompression
H. Baba, Yasuhisa Maezawa, Kenzo Uchida, Nobuaki Furusawa, Makoto Wada, Shinichi Imura
Upside-down reversal of vision in multiple sclerosis
Çig˘dem F. Dog˘ulu, Tülay Kansu
Nerve biopsy findings in hemizygous and heterozygous patients with Fabry’s disease
Keiko Toyooka, Gérard Said
Pulsed high-dose dexamethasone treatment of polyneuropathy associated with monoclonal gammopathy
N. C. Notermans, M. Vermeulen, H. M. Lokhorst, P. A. Van Doorn, L. H. Van den Berg, L. L. Teunissen, J. H. J. Wokke
Maternally inherited diabetes and deafness with cerebellar ataxia: a new clinical phenotype associated with the mitochondrial DNA 3243 mutation
M. Arai, Shin-ichi Ohshima
Delayed-onset hemidystonia secondary to herpes zoster ophthalmicus-related intracerebral arteritis in an adolescent
P. Burbaud, J. Berge, A. Lagueny, A. Mensire, M. Melon, J. M. Caillé, B. Bioulac