- Homocysteine and holotranscobalamin and the risk of Alzheimer disease A longitudinal study
[作者：Hooshmand, B; Solomon, A; Kareholt, I; Leiviska, J; Rusanen, M; Ahtiluoto, S; Winblad, B; Laatikainen, T; Soininen, H; Kivipelto, M,期刊：Neurology, 页码：1408-1414 , 文章类型： Article，,卷期：2010年75-16]
- Objective: To examine the relation between serum levels of homocysteine (tHcy) and holotranscobalamin (holoTC), the active fraction of vitamin B12, and risk of incident Alzheimer disease (AD) in a sample of Finnish commu...
- Physical activity predicts gray matter volume in late adulthood The Cardiovascular Health Study
[作者：Erickson, KI; Raji, CA; Lopez, OL; Becker, JT; Rosano, C; Newman, AB; Gach, HM; Thompson, PM; Ho, AJ; Kuller, LH,期刊：Neurology, 页码：1415-1422 , 文章类型： Article，,卷期：2010年75-16]
- Objectives: Physical activity (PA) has been hypothesized to spare gray matter volume in late adulthood, but longitudinal data testing an association has been lacking. Here we tested whether PA would be associated with gr...
- IFN beta-1b may severely exacerbate Japanese optic-spinal MS in neuromyelitis optica spectrum
[作者：Shimizu, J; Hatanaka, Y; Hasegawa, M; Iwata, A; Sugimoto, I; Date, H; Goto, J; Shimizu, T; Takatsu, M; Sakurai, Y; Nakase, H; Uesaka, Y; Hashida, H; Hashimoto, K; Komiya, T; Tsuji, S,期刊：Neurology, 页码：1423-1427 , 文章类型： Article，,卷期：2010年75-16]
- Background: Interferon-beta-1b (IFN beta-1b) has been used to prevent exacerbation of relapsing-remitting multiple sclerosis (RRMS) including optic-spinal multiple sclerosis (OSMS) in Japan. We encountered 2 patients wit...
- Premorbid cognitive leisure independently contributes to cognitive reserve in multiple sclerosis
[作者：Sumowski, JF; Wylie, GR; Gonnella, A; Chiaravalloti, N; DeLuca, J,期刊：Neurology, 页码：1428-1431 , 文章类型： Article，,卷期：2010年75-16]
- Objective: Consistent with the cognitive reserve hypothesis, higher education and vocabulary help persons with Alzheimer disease (AD) and multiple sclerosis (MS) better withstand neuropathology before developing cognitiv...
- Prevalence of multiple sclerosis in Korea
[作者：Kim, NH; Kim, HJ; Cheong, HK; Kim, BJ; Lee, KH; Kim, EH; Kim, EA; Kim, S; Park, MS; Yoon, WT,期刊：Neurology, 页码：1432-1438 , 文章类型： Article，,卷期：2010年75-16]
- Objective: The aim of this study was to estimate the prevalence of multiple sclerosis (MS) in Korea through a nationwide survey.Methods: We estimated the prevalence of MS in Korea using several sources collected between ...
- Pain in Guillain-Barre syndrome A long-term follow-up study
[作者：Ruts, L; Drenthen, J; Jongen, JLM; Hop, WCJ; Visser, GH; Jacobs, BC; Doorn, PA,期刊：Neurology, 页码：1439-1447 , 文章类型： Article，,卷期：2010年75-16]
- Background: Pain in Guillain-Barre syndrome (GBS) may be pronounced and is often overlooked. Objectives: To obtain detailed information about pain in GBS and its clinical variants.Methods: This was a prospective cohort s...
- Predictors of seizure freedom after incomplete resection in children
[作者：Perry, MS; Dunoyer, C; Dean, P; Bhatia, S; Bavariya, A; Ragheb, J; Miller, I; Resnick, T; Jayakar, P; Duchowny, M,期刊：Neurology, 页码：1448-1453 , 文章类型： Article，,卷期：2010年75-16]
- Objective: Incomplete resection of the epileptogenic zone (EZ) is the most important predictor of poor outcome after resective surgery for intractable epilepsy. We analyzed the contribution of preoperative and perioperat...
- SCN2A mutation associated with neonatal epilepsy, late-onset episodic ataxia, myoclonus, and pain
[作者：Liao, Y; Anttonen, AK; Liukkonen, E; Gaily, E; Maljevic, S; Schubert, S; Bellan-Koch, A; Petrou, S; Ahonen, VE; Lerche, H; Lehesjoki, AE,期刊：Neurology, 页码：1454-1458 , 文章类型： Article，,卷期：2010年75-16]
- Background: Inherited and de novo mutations in sodium channel genes underlie a variety of channelopathies. Mutations in SCN2A, encoding the brain sodium channel Na(V)1.2, have previously been reported to be associated wi...
- Pontocerebellar hypoplasia Clinical, pathologic, and genetic studies
[作者：Cassandrini, D; Biancheri, R; Tessa, A; Di Rocco, M; Di Capua, M; Bruno, C; Denora, PS; Sartori, S; Rossi, A; Nozza, P; Emma, F; Mezzano, P; Politi, MR; Laverda, AM; Zara, F; Pavone, L; Simonati, A; Leuzzi, V; Santorelli, FM; Bertini, E,期刊：Neurology, 页码：1459-1464 , 文章类型： Article，,卷期：2010年75-16]
- Background: Mutations in genes encoding subunits of the tRNA-splicing endonuclease (TSEN) complex were identified in patients with pontocerebellar hypoplasia 2 (PCH2) and pontocerebellar hypoplasia 4 (PCH4). Objective: W...
- Transcranial magnetic brain stimulation modulates blepharospasm A randomized controlled study
[作者：Kranz, G; Shamim, EA; Lin, PT; Kranz, GS; Hallett, M,期刊：Neurology, 页码：1465-1471 , 文章类型： Article，,卷期：2010年75-16]
- Background: Benign essential blepharospasm (BEN is a common form of focal dystonia. Besides pathology in the basal ganglia, accumulating evidence suggests pathologic changes in the anterior cingulate cortex (ACC).Methods...
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