Publisher: Wiley-Blackwell

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Volume 116, Number 6, December 2007

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Posterior cortical brain dysfunction in cognitively impaired patients with Parkinson’s disease – a rCBF scintigraphy study
pp. 347-354(8)
Authors: Wallin, A.; Ekberg, S.; Lind, K.; Milos, V.; Granérus, A.-K.; Granerus, G.

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Emotional arousal enhances declarative memory in patients with Alzheimer’s disease
pp. 355-360(6)
Authors: Satler, C.; Garrido, L. M.; Sarmiento, E. P.; Leme, S.; Conde, C.; Tomaz, C.

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Prevalence of epilepsy in Croatia: a population-based survey
pp. 361-367(7)
Authors: Bielen, I.; Cvitanovic-Sojat, L.; Bergman-Markovic, B.; Kosicek, M.; Planjar-Prvan, M.; Vuksic, L.; Miketek, G.; Matek, P.

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Nitric oxide synthase and NMDA receptor expressions in cavernoma tissues with epileptogenesis
pp. 368-373(6)
Authors: Kamida, T.; Takeda, Y.; Fujiki, M.; Abe, T.; Abe, E.; Kobayashi, H.

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Circulating interleukin-15 and RANTES chemokine in Parkinson’s disease
pp. 374-379(6)
Authors: Rentzos, M.; Nikolaou, C.; Andreadou, E.; Paraskevas, G. P.; Rombos, A.; Zoga, M.; Tsoutsou, A.; Boufidou, F.; Kapaki, E.; Vassilopoulos, D.

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Serum levels of glial fibrillary acidic protein correlate to tumour volume of high-grade gliomas
pp. 380-384(5)
Authors: Brommeland, T.; Rosengren, L.; Fridlund, S.; Hennig, R.; Isaksen, V.

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Schizotypal personality traits in Gilles de la Tourette syndrome
pp. 385-391(7)
Authors: Cavanna, A. E.; Robertson, M. M.; Critchley, H. D.

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The APOE polymorphism and 1-year outcome in ischemic stroke: genotype–gender interaction
pp. 392-398(7)
Authors: Gromadzka, G.; Baranska-Gieruszczak, M.; Sarzynska-Dlugosz, I.; Ciesielska, A.; Czlonkowska, A.

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A comparison of sural nerve conduction studies in patients with impaired oral glucose tolerance test
pp. 399-405(7)
Authors: Koçer, A.; Domaç, F. M.; Boylu, E.; Us, Ö.; Tanridağ, T.

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Long-term effect of intravenous immunoglobulin on anti-MuSK antibody-positive myasthenia gravis
pp. 406-408(3)
Authors: Shibata-Hamaguchi, A.; Samuraki, M.; Furui, E.; Iwasa, K.; Yoshikawa, H.; Hayashi, S.; Yamada, M.

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Serum levels and genetic variation of TGF-β1 are not associated with Alzheimer’s disease
pp. 409-412(4)
Authors: Rodríguez-Rodríguez, E.; Sánchez-Juan, P.; Mateo, I.; Llorca, J.; Infante, J.; García-Gorostiaga, I.; Berciano, J.; Combarros, O.

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MECP2 mutations in Serbian Rett syndrome patients
pp. 413-419(7)
Authors: Djarmati, A.; Dobričić, V.; Kecmanović, M.; Marsh, P.; Jančić-Stefanović, J.; Klein, C.; Djurić, M.; Romac, S.

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