Publisher: Elsevier

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Volume 157, Number 2, 7 May 1998

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Modulation of ICAM-1, VCAM-1 and HLA-DR by cytokines and steroids on HUVECs and human brain endothelial cells
pp. 117-121(5)
Authors: Dufour, A.; Corsini, E.; Gelati, M.; Ciusani, E.; Zaffaroni, M.; Giombini, S.; Massa, G.; Salmaggi, A.

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Multiple sclerosis with mite antigen-specific IgE
pp. 138-142(5)
Authors: Kira J.-i.; Kawano, Y.; Yamasaki, K.

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Late-onset sporadic progressive subcortical gliosis
pp. 143-147(5)
Authors: Lanska, D.J.; Markesbery, W.R.; Cochran, E.; Bennett, D.; Lanska, M.J.; Cohen, M.

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Diagnosis of herpes simplex encephalitis by magnetic resonance imaging and polymerase chain reaction assay of cerebrospinal fluid
pp. 148-153(6)
Authors: Domingues, R.B.; Fink, M.C.D.; Tsanaclis, A.M.C.; de Castro, C.C.; Cerri, G.G.; Mayo, M.S.; Lakeman, F.D.

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The spinal cord descending pathway for micturition: analysis in patients with spinal cord infarction
pp. 154-157(4)
Authors: Inatomi, Y.; Itoh, Y.; Fujii, N.; Nakanishi, K.

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Determinants of cognitive disorders in Autosomal Dominant Cerebellar Ataxia type 1
pp. 162-167(6)
Authors: Trojano, L.; Chiacchio, L.; Grossi, D.; Pisacreta, A.I.; Calabrese, O.; Castaldo, I.; de Michele, G.; Filla, A.

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Intrathecal activation of the complement system and disability in multiple sclerosis
pp. 168-174(7)
Authors: Sellebjerg, F.; Jaliashvili, I.; Christiansen, M.; Garred, P.

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Natural killer cells in patients with Guillain-Barre syndrome
pp. 175-178(4)
Authors: Yoshii, F.; Shinohara, Y.

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Molecular characterisation of Duchenne muscular dystrophy and phenotypic correlation
pp. 179-186(8)
Authors: Mital, A.; Kumari, D.; Gupta, M.; Goyle, S.

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Serum gelsolin and rhabdomyolysis
pp. 187-190(4)
Authors: Lofberg, M.; Paunio, T.; Tahtela, R.; Kiuru, S.; Somer, H.

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The importance of electrodiagnostic studies in acute organophosphate poisoning
pp. 191-200(10)
Authors: Singh, G.; Mahajan, R.; Whig, J.

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Pyruvate dehydrogenase complex deficiency and altered respiratory chain function in a patient with Kearns-Sayre/MELAS overlap syndrome and A3243G mtDNA mutation
pp. 206-213(8)
Authors: Wilichowski, E.; Christoph Korenke, G.; Ruitenbeek, W.; de Meirleir, L.; Hagendorff, A.; Janssen, A.J.M.; Lissens, W.; Hanefeld, F.

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Kleine-Levin syndrome and Parkinsonian symptoms - a case report
pp. 214-216(3)
Authors: Muller, T.; Kuhn, W.; Bornke, C.; Buttner, T.; Przuntek, H.

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Unusual association of multiple sclerosis and tomaculous neuropathy
pp. 217-222(6)
Authors: Drulovic, J.; Dozic, S.; Levic, Z.; Stojsavljevic, N.; Trikic, R.; Cvetkovic, D.; Apostolski, S.

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