European Journal of Neurology

Calendar
pp. i-i(1)

Instructions for Authors
pp. ii-iii(2)

Bilateral pulvinar thalamic calcification in a patient with chronic cryptococcal meningitis
pp. e1-e2(2)
Authors: Sahraian, M. A.; Motamedi, M.; Azimi, A. R.; Hasan Paknejad, S. M.

IP-10 serum levels are not increased in mild cognitive impairment and Alzheimer's disease
pp. e3-e4(2)
Authors: Galimberti, D.; Venturelli, E.; Fenoglio, C.; Lovati, C.; Guidi, I.; Scalabrini, D.; Mariani, C.; Bresolin, N.; Scarpini, E.

Cerebral venous thrombosis associated with repeated use of emergency contraception
pp. e5-e5(1)
Authors: Horga, A.; Santamarina, E.; Quilez, A.; de Francisco, J.; Garcia-Martinez, R.; Alvarez-Sabin, J.

Persistent anarthria following mirror infarction in the anterior choroidal artery territory
pp. e6-e6(1)
Authors: Boes, M.; Urbach, H.; Klockgether, T.; Schlegel, U.

Acquired prothrombotic state due to protein-losing enteropathy as a rare cause for ischemic stroke?
pp. e7-e8(2)
Authors: Amtage, F.; Marouf, W.; Hetzel, A.; Schubert, M.

Responsiveness to a dopamine agent in Holmes tremor - case report
pp. e9-e10(2)
Authors: Strecker, K.; Schneider, J. P.; Sabri, O.; Wegner, F.; Then Bergh, F.; Schwarz, J.; Hesse, S.

The protein load of therapeutic botulinum toxins
pp. e11-e11(1)
Authors: Pickett, A.; O'Keeffe, R.; Panjwani, N.

Law and the Brain
pp. e12-e12(1)
Author: Jellinger, K. A.

Multiple Sclerosis and Demyelinating Diseases
pp. e13-e13(1)
Author: Jellinger, K.A.

From Basic Pain Mechanisms to Headache
pp. e14-e14(1)
Author: Jellinger, K. A.

The Nerve Tower. A Neurological Time Journey
pp. e15-e15(1)
Author: Jellinger, K. A.

Stroke Medicine
pp. e16-e16(1)
Author: Jellinger, K. A.

Molecular imaging in hereditary forms of parkinsonism
pp. 359-368(10)
Authors: Shih, M. C.; Felicio, A. C.; de Oliveira Godeiro-Junior, C.; de Carvalho Aguiar, P.; de Andrade, L. A. F.; Ferraz, H. B.; Bressan, R. A.

Juvenile-onset neuronal ceroid lipofuscinosis with infantile CLN1 mutation and palmitoyl-protein thioesterase deficiency
pp. 369-372(4)
Authors: Kälviäinen, R.; Eriksson, K.; Losekoot, M.; Sorri, I.; Harvima, I.; Santavuori, P.; Järvelä, I.; Autti, T.; Vanninen, R.; Salmenperä, T.; van Diggelen, O. P.

Blood pressure and heart rate in parkinsonian patients with and without wearing-off
pp. 373-378(6)
Authors: Pursiainen, V.; Korpelainen, J. T.; Haapaniemi, T. H.; Sotaniemi, K. A.; Myllylä, V. V.

Metabolic syndrome is more associated with intracranial atherosclerosis than extracranial atherosclerosis
pp. 379-386(8)
Authors: Park, J.-H.; Kwon, H.-M.; Roh, J.-K.

Slowly progressive hemiparesis in childhood as a consequence of Rasmussen encephalitis without or with delayed-onset seizures
pp. 387-390(4)
Authors: Bien, C. G.; Elger, C. E.; Leitner, Y.; Gomori, M.; Ran, B.; Urbach, H.; Wilken, B.; Korn-Lubetzki, I.

Treatment of newly diagnosed symptomatic pure low-grade oligodendrogliomas with PCV chemotherapy
pp. 391-398(8)
Authors: Lebrun, C.; Fontaine, D.; Bourg, V.; Ramaioli, A.; Chanalet, S.; Vandenbos, F.; Lonjon, M.; Fauchon, F.; Paquis, P.; Frenay, M.

Neurological negligence claims in the NHS from 1995 to 2005
pp. 399-402(4)
Author: McNeill, A.

Clinical and demographical characteristics of primary progressive multiple sclerosis in Isfahan, Iran
pp. 403-407(5)
Authors: Maghzi, A. H.; Etemadifar, M.; Saadatnia, M.

Hepatocellular carcinoma presenting as nervous system involvement
pp. 408-412(5)
Authors: Chen, S.-F.; Tsai, N.-W.; Lui, C.-C.; Lu, C.-H.; Huang, C.-R.; Chuang, Y.-C.; Cheng, Y.-F.; Kuo, C.-H.; Chang, W.-N.

A common leucine-rich repeat kinase 2 gene mutation in familial and sporadic Parkinson's disease in Russia
pp. 413-417(5)
Authors: Illarioshkin, S. N.; Shadrina, M. I.; Slominsky, P. A.; Bespalova, E. V.; Zagorovskaya, T. B.; Bagyeva, G. Kh.; Markova, E. D.; Limborska, S. A.; Ivanova-Smolenskaya, I. A.

Human immunodeficiency virus-associated progressive multifocal leucoencephalopathy: epidemiology and predictive factors for prolonged survival
pp. 418-423(6)
Authors: Drake, A. K.; Loy, C. T.; Brew, B. J.; Chen, T. C. C.; Petoumenos, K.; Li, P. C. K.; Wright, E. J.

Genetic variants in the IMPA2 gene do not confer increased risk of febrile seizures in Caucasian patients
pp. 424-427(4)
Authors: Blair, M. A.; Ma, S.; Abou-Khalil, B.; Hedera, P.

A polymorphism of the aldehyde dehydrogenase 2 gene is a risk factor for multiple lacunar infarcts in Japanese men: the Takahata Study
pp. 428-434(7)
Authors: Nagasawa, H.; Wada, M.; Arawaka, S.; Kawanami, T.; Kurita, K.; Daimon, M.; Adachi, M.; Hosoya, T.; Emi, M.; Muramatsu, M.; Kato, T.

One-year outcome after first-ever stroke according to stroke subtype, severity, risk factors and pre-stroke treatment. A population-based study from Tartu, Estonia
pp. 435-439(5)
Authors: Vibo, R.; Kõrv, J.; Roose, M.

Cognitive and behavioural predictors of progression rates in Alzheimer's disease
pp. 440-446(7)
Authors: Buccione, I.; Perri, R.; Carlesimo, G. A.; Fadda, L.; Serra, L.; Scalmana, S.; Caltagirone, C.

Thalami and corona radiata in juvenile NCL (CLN3): a voxel-based morphometric study
pp. 447-450(4)
Authors: Autti, T.; Hämäläinen, J.; Åberg, L.; Lauronen, L.; Tyynelä, J.; Van Leemput, K.

Cerebral embolism with interventional closure of symptomatic patent foramen ovale: An MRI-based study using diffusion-weighted imaging
pp. 451-454(4)
Authors: Dorenbeck, U.; Simon, B.; Skowasch, D.; Stüßer, C.; Gockel, A.; Schild, H. H.; Urbach, H.; Bauriedel, G.

Insight and danger in Alzheimer's disease
pp. 455-460(6)
Authors: Starkstein, S. E.; Jorge, R.; Mizrahi, R.; Adrian, J.; Robinson, R. G.

Paroxysmal sneezing at the onset of lateral medullary syndrome: cause or consequence?
pp. 461-463(3)
Authors: Swenson, A. J.; Leira, E. C.

Novel mutation of the Notch3 gene in a Japanese patient with CADASIL
pp. 464-466(3)
Authors: Oki, K.; Nagata, E.; Ishiko, A.; Shimizu, A.; Tanaka, K.; Takahashi, K.; Tabira, T.; Katayama, T.; Suzuki, N.

Variant Creutzfeldt-Jakob disease: first two indigenous cases in Republic of Ireland. Case report and perspective
pp. 467-469(3)
Authors: McHugh, J. C.; Bradley, D.; Hutchinson, M.; Brett, F.; Heffernan, J.; Howley, R.; Farrell, M.; Tubridy, N.

Turcot syndrome confirmed with molecular analysis
pp. 470-472(3)
Authors: Lebrun, C.; Olschwang, S.; Jeannin, S.; Vandenbos, F.; Sobol, H.; Frenay, M.

Pure word deafness and pure anarthria in a patient with frontotemporal dementia
pp. 473-475(3)
Authors: Iizuka, O.; Suzuki, K.; Endo, K.; Fujii, T.; Mori, E.

ERRATUM
pp. 476-476(1)