Ausgabe 4/2006
Inhalt (11 Artikel)
ORIGINAL
Expression of multidrug resistance type 1 gene (MDR1) P-glycoprotein in intractable epilepsy with different aetiologies: a double-labelling and electron microscopy study
D. Chengyun, L. Guoming, M. Elia, M. V. Catania, X. Qunyuan
ORIGINAL
Two novel Italian CADASIL families from Central Italy with mutation CGC-TGC at codon 1006 in the exon 19 Notch3 gene
M. Ragno, G. M. Fabrizi, G. Cacchiò, M. Scarcella, G. Sirocchi, F. Selvaggio, F. Taioli, M. Ferrarini, L. Trojano
ORIGINAL
Human T-cell lymphotropic virus type I (HTLV-I) confirmed by PCR-Southern blot and sequencing analysis in a woman with tropical spastic paraparesis
F. Perandin, A. Cariani, C. Bonfanti, L. Trainini, M. Magoni, N. Manca
ORIGINAL
Pravastatin in vivo reduces mononuclear cell migration through endothelial monolayers
S. Frigerio, M. Gelati, G. Boncoraglio, E. Ciusani, D. Croci, M. de Curtis, E. Parati, A. Salmaggi
UPDATE IN NEUROGENETICS
The spectrum of mutations for the diagnosis of vanishing white matter disease
O. Scali, C. Di Perri, A. Federico
CASE REPORT
Isolated bilateral anterior optic neuritis following chickenpox in an immunocompetent adult
A. Galbussera, E. Tagliabue, M. Frigo, P. Apale, C. Ferrarese, I. Appollonio
CASE REPORT
Meningitis following relapsing painful ophthalmoplegia in aspergillus sphenoidal sinusitis: a case report
A. Botturi, A. Salmaggi, B. Pollo, E. Lamperti, A. Erbetta, A. Boiardi
CASE REPORT
Isolated oculomotor nerve palsy as the presenting clinical manifestation of a meningeal carcinomatosis: a case report
R. Nardone, M. Herz, E. Egarter-Vigl, F. Tezzon
LETTER
Spontaneous bilateral carotid artery dissection and hereditary haemochromatosis: what relationship?
S. Gallerini, N. Morelli, A. Chiti, F. Baldacci, C. Sonnoli, G. Orlandi, L. Murri