Publisher: Elsevier

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Volume 196, Number 1, 15 April 2002

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Sialosyl-galactose: a common denominator of Guillain-Barre and related disorders?
pp. 1-7(7)
Authors: Moran, A.P.; Prendergast, M.M.; Hogan, E.L.

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Very early activation of m-calpain in peripheral nerve during Wallerian degeneration
pp. 9-20(12)
Authors: Glass, J.D.; Culver, D.G.; Levey, A.I.; Nash, N.R.

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Up-regulation of interleukin-12 receptor expression in peripheral blood mononuclear cells of patients with HTLV-I-associated myelopathy/tropical spastic paraparesis
pp. 21-26(6)
Authors: Fujimoto, T.; Nakamura, T.; Nishiura, Y.; Ichinose, K.; Furuya, T.; Shirabe, S.; Eguchi, K.

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Hypercortisolemia in acute stroke is related to the inflammatory response
pp. 27-32(6)
Authors: Slowik, A.; Turaj, W.; Pankiewicz, J.; Dziedzic, T.; Szermer, P.; Szczudlik, A.

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Restless legs syndrome in Parkinson's disease
pp. 33-36(4)
Authors: Tan, E.K.; Lum, S.Y.; Wong, M.C.

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Diffusion MRI in three types of anoxic encephalopathy
pp. 37-40(4)
Authors: Singhal, A.B.; Topcuoglu, M.A.; Koroshetz, W.J.

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Detection of anti-ganglioside antibodies in Guillain-Barre syndrome and its variants by the agglutination assay
pp. 41-44(4)
Authors: Alaedini, A.; Briani, C.; Wirguin, I.; Siciliano, G.; D'Avino, C.; Latov, N.

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Cytoskeleton abnormalities in axonopathies of unknown aetiology: correlations with morphometry
pp. 53-61(9)
Authors: Fressinaud, C.; Vigneron, I.; Letournel, F.; Nicolas, G.; Jean, I.; Dubas, F.

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Subtype analysis of neuropathologically diagnosed patients in a Japanese geriatric hospital
pp. 63-69(7)
Authors: Akatsu, H.; Takahashi, M.; Matsukawa, N.; Ishikawa, Y.; Kondo, N.; Sato, T.; Nakazawa, H.; Yamada, T.; Okada, H.; Yamamoto, T.; Kosaka, K.

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Severe involvement of the ambient gyrus in a case of dementia with argyrophilic grain disease
pp. 71-75(5)
Authors: Saito, Y.; Yamazaki, M.; Kanazawa, I.; Murayama, S.

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Neurotologic manifestations of the fibromyalgia syndrome
pp. 77-80(4)
Authors: Bayazit, Y.A.; Gursoy, S.; Ozer, E.; Karakurum, G.; Madenci, E.

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Cold pressor test demonstrates residual sympathetic cardiovascular activation in familial dysautonomia
pp. 81-89(9)
Authors: Hilz, M.J.; Axelrod, F.B.; Braeske, K.; Stemper, B.

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Cerebral cavernous malformation: novel mutation in a Chinese family and evidence for heterogeneity
pp. 91-96(6)
Authors: Chen, D.; Lipe, H.P.; Qin, Z.; Bird, T.D.

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