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Volume 15, Number 10, October 2008

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Calendar
pp. i-i(1)

Stroke and multiple peripheral thrombotic events in an adult with varicella
pp. e90-e91(2)
Authors: Massano, J.; Ferreira, D.; Toledo, T.; Mansilha, A.; Azevedo, E.; Carvalho, M.

Ptosis, diplopia and statins: an association?
pp. e92-e93(2)
Authors: Elsais, A.; Lund, C.; Kerty, E.

AAN-EFNS guidelines on trigeminal neuralgia management
pp. 1013-1028(16)
Authors: Cruccu, G.; Gronseth, G.; Alksne, J.; Argoff, C.; Brainin, M.; Burchiel, K.; Nurmikko, T.; Zakrzewska, J. M.

Paraneoplastic myasthenia gravis: immunological and clinical aspects
pp. 1029-1033(5)
Authors: Skeie, G. O.; Romi, F.

Misdiagnosis in epilepsy: a review and recognition of diagnostic uncertainty
pp. 1034-1042(9)
Authors: Chowdhury, F. A.; Nashef, L.; Elwes, R. D. C.

Reduced oxygen due to high-altitude exposure relates to atrophy in motor-function brain areas
pp. 1050-1057(8)
Authors: Paola, M. D.; Bozzali, M.; Fadda, L.; Musicco, M.; Sabatini, U.; Caltagirone, C.

A 1H magnetic resonance spectroscopy study in patients with obstructive sleep apnea
pp. 1058-1064(7)
Authors: Sarchielli, P.; Presciutti, O.; Alberti, A.; Tarducci, R.; Gobbi, G.; Galletti, F.; Costa, C.; Eusebi, P.; Calabresi, P.

Clinical heterogeneity and genotype-phenotype correlations in hereditary spastic paraplegia because of Spatacsin mutations (SPG11)
pp. 1065-1070(6)
Authors: Paisan-Ruiz, C.; Nath, P.; Wood, N. W.; Singleton, A.; Houlden, H.

Adapted Finnish Migraine-Specific Questionnaire for family studies (FMSQFS): a validation study in two languages
pp. 1071-1074(4)
Authors: Facheris, M. F.; Vogl, F. D.; Hollmann, S.; Sixt, G.; Pattaro, C.; Schönhuber, R.; Pramstaller, P. P.

Epidemiological study of acute encephalitis in Tottori Prefecture, Japan
pp. 1075-1079(5)
Authors: Wada-Isoe, K.; Kusumi, M.; Kai, T.; Awaki, E.; Shimoda, M.; Yano, H.; Suzuki, K.; Nakayasu, H.; Oota, K.; Kowa, H.; Nakashima, K.

Cytokine IL-1 beta but not IL-1 alpha promoter polymorphism is associated with Alzheimer disease in a population from the Canary Islands, Spain
pp. 1080-1084(5)
Authors: Déniz-Naranjo, M. C.; Muñoz-Fernandez, C.; Alemany-Rodríguez, M. J.; Pérez-Vieitez, M. C.; Aladro-Benito, Y.; Irurita-Latasa, J.; Sánchez-García, F.

Blood pressure is not associated with haematoma enlargement in acute intracerebral haemorrhage
pp. 1085-1090(6)
Authors: Martí-Fàbregas, J.; Martínez-Ramírez, S.; Martínez-Corral, M.; Díaz-Manera, J.; Querol, L.; Suárez-Calvet, M.; de Juan, M.; Santaló, M.; Marín, R.; Martí-Vilalta, J.-L.

Brain atrophy as a marker of cognitive impairment in mildly disabling relapsing-remitting multiple sclerosis
pp. 1091-1099(9)
Authors: Sánchez, M. P.; Nieto, A.; Barroso, J.; Martín, V.; Hernández, M. A.

The role of IL-12 and TNF-α in AIDP and AMAN
pp. 1100-1105(6)
Authors: Deng, H.; Yang, X.; Jin, T.; Wu, J.; Hu, L.-S.; Chang, M.; Sun, X.-J.; Adem, A.; Winblad, B.; Zhu, J.

Concordance and heritability of multiple sclerosis in Finland: study on a nationwide series of twins
pp. 1106-1110(5)
Authors: Kuusisto, H.; Kaprio, J.; Kinnunen, E.; Luukkaala, T.; Koskenvuo, M.; Elovaara, I.

Novel exon 1 progranulin gene variant in Alzheimer's disease
pp. 1111-1117(7)
Authors: Cortini, F.; Fenoglio, C.; Guidi, I.; Venturelli, E.; Pomati, S.; Marcone, A.; Scalabrini, D.; Villa, C.; Clerici, F.; Dalla Valle, E.; Mariani, C.; Cappa, S.; Bresolin, N.; Scarpini, E.; Galimberti, D.

Mechanism of tuberothalamic infarction
pp. 1118-1123(6)
Authors: Kim, J.; Choi, H.-Y.; Nam, H. S.; Lee, J. Y.; Heo, J. H.

A novel presenilin 2 mutation (V393M) in early-onset dementia with profound language impairment
pp. 1135-1139(5)
Authors: Lindquist, S. G.; Hasholt, L.; Bahl, J. M. C.; Heegaard, N. H. H.; Andersen, B. B.; Nørremølle, A.; Stokholm, J.; Schwartz, M.; Batbayli, M.; Laursen, H.; Pardossi-Piquard, R.; Chen, F.; St George-Hyslop, P.; Waldemar, G.; Nielsen, J. E.

Charcot-Marie-Tooth type X: unusual phenotype of a novel CX32 mutation
pp. 1140-1142(3)
Authors: Mazzeo, A.; Di Leo, R.; Toscano, A.; Muglia, M.; Patitucci, A.; Messina, C.; Vita, G.

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