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Volume 14, Number 12, December 2007

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Calendar
pp. i-i(1)

Instructions for Authors
pp. ii-iii(2)

Opsoclonus myoclonus syndrome in two cases with neuroborreliosis
pp. e1-e2(2)
Authors: Skeie, G. O.; Eldøen, G.; Skeie, B. S.; Midgard, R.; Kristoffersen, E. K.; Bindoff, L. A.

Aseptic meningitis associated with lamotrigine: report of two cases
pp. e3-e4(2)
Authors: Nesseler, N.; Polard, E.; Arvieux, C.; Coquerel, N.; Michelet, C.; Tattevin, P.

Preferential involvement of the basolateral limbic circuit in an amyotrophic lateral sclerosis patient
pp. e5-e6(2)
Authors: Takeda, T.; Uchihara, T.; Chikugo, T.; Hiraga, T.; Kitaguchi, M.; Kojima, H.

Valproic acid treatment in six patients with spinal muscular atrophy
pp. e8-e9(2)
Authors: Tsai, L.-K.; Yang, C.-C.; Hwu, W.-L.; Li, H.

EFNS guideline on diagnosis and management of limb girdle muscular dystrophies
pp. 1305-1312(8)
Authors: Norwood, F.; de Visser, M.; Eymard, B.; Lochmüller, H.; Bushby, K.

Chronic high dose transdermal nicotine in Parkinson's disease: an open trial
pp. 1313-1316(4)
Authors: Villafane, G.; Cesaro, P.; Rialland, A.; Baloul, S.; Azimi, S.; Bourdet, C.; Le Houezec, J.; Macquin-Mavier, I.; Maison, P.

Prescribing patterns of antiepileptic drugs in Italy: a nationwide population-based study in the years 2000-2005
pp. 1317-1321(5)
Authors: Savica, R.; Beghi, E.; Mazzaglia, G.; Innocenti, F.; Brignoli, O.; Cricelli, C.; Caputi, A. P.; Musolino, R.; Spina, E.; Trifirò, G.

Isoform-specific increase of spastin stability by N-terminal missense variants including intragenic modifiers of SPG4 hereditary spastic paraplegia
pp. 1322-1328(7)
Authors: Schickel, J.; Pamminger, T.; Ehrsam, A.; Münch, S.; Huang, X.; Klopstock, T.; Kurlemann, G.; Hemmerich, P.; Dubiel, W.; Deufel, T.; Beetz, C.

Cerebrospinal fluid neurofilament light levels in amyotrophic lateral sclerosis: impact of SOD1 genotype
pp. 1329-1333(5)
Authors: Zetterberg, H.; Jacobsson, J.; Rosengren, L.; Blennow, K.; Andersen, P. M.

Topiramate: effects on serum lipids and lipoproteins levels in children
pp. 1334-1337(4)
Authors: Franzoni, E.; Verrotti, A.; Sarajlija, J.; Garone, C.; Matricardi, S.; Salerno, G. G.; Monti, M.; Chiarelli, F.

A prospective study of patterns of fatigue in multiple sclerosis
pp. 1338-1343(6)
Authors: Lerdal, A.; Gulowsen Celius, E.; Krupp, L.; Dahl, A. A.

Cognitive changes in asymptomatic carriers of the Huntington disease mutation gene
pp. 1344-1350(7)
Authors: Verny, C.; Allain, P.; Prudean, A.; Malinge, M.-C.; Gohier, B.; Scherer, C.; Bonneau, D.; Dubas, F.; Le Gall, D.

Ischaemic stroke - impact of renal dysfunction on in-hospital mortality
pp. 1351-1356(6)
Authors: Fabjan, T. Hojs; Hojs, R.; Tetičkovič, E.; Balon, B. Pečovnik

Migraine and delayed ischaemic neurological deficit after subarachnoid haemorrhage in women: a case-control study
pp. 1363-1368(6)
Authors: Dreier, J. P.; Kremer, C.; Lammers, G.; Lohmann, F.; Hansen, H. C.; Valdueza, J. M.

Radiotherapy reduces sialorrhea in amyotrophic lateral sclerosis
pp. 1373-1377(5)
Authors: Neppelberg, E.; Haugen, D. F.; Thorsen, L.; Tysnes, O.-B.

Acute subcortical stroke and early serotonergic modification: a IDAP study
pp. 1378-1382(5)
Authors: Rocco, A.; Afra, J.; Toscano, M.; Sirimarco, G.; Di Clemente, L.; Altieri, M.; Lenzi, G. L.; Di Piero, V.

Imbalances in circulating lymphocyte subsets in Hu antibody associated paraneoplastic neurological syndromes
pp. 1383-1391(9)
Authors: de Beukelaar, J. W.; Smitt, P. A. Sillevis; Hop, W. C.; Kraan, J.; Hooijkaas, H.; Verjans, G. M. G. M.; Gratama, J. W.

X chromosome inactivation in females with multiple sclerosis
pp. 1392-1396(5)
Authors: Knudsen, G. P. S.; Harbo, H. F.; Smestad, C.; Celius, E. G.; Åkesson, E.; Oturai, A.; Ryder, L. P.; Spurkland, A.; Ørstavik, K. H.

Intercellular adhesion molecule-1 gene polymorphism in Iranian patients with multiple sclerosis
pp. 1397-1399(3)
Authors: Mousavi, S. A. R.; Nikseresht, A. R.; Arandi, N.; Borhani Haghighi, A.; Ghaderi, A.

Reversible dementia and corresponding CSF alterations due to intraspinal lumbosacral metastasis of a prostate carcinoma
pp. 1400-1402(3)
Authors: Winkler, F.; Gschwendtner, A.; Theisen, D.; Peraud, A.; Straube, A.

Clinical features of patients with myasthenia gravis associated with autoimmune diseases
pp. 1403-1404(2)
Authors: Kanazawa, M.; Shimohata, T.; Tanaka, K.; Nishizawa, M.

Autonomic dysfunction in 3414 Parkinson's disease patients enrolled in the German Network on Parkinson's disease (KNP e.V.): the effect of ageing
pp. 1405-1408(4)
Authors: Wüllner, U.; Schmitz-Hübsch, T.; Antony, G.; Fimmers, R.; Spottke, A.; Oertel, W. H.; Deuschl, G.; Klockgether, T.; Eggert, K.

A novel mutation in the PSEN1 gene (L286P) associated with familial early-onset dementia of Alzheimer type and lobar haematomas
pp. 1409-1412(4)
Authors: Sánchez-Valle, R.; Lladó, A.; Ezquerra, M.; Rey, M. J.; Rami, L.; Molinuevo, J. L.

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