- Red blood cell omega-3 fatty acid levels and markers of accelerated brain aging
[作者：Tan, ZS; Harris, WS; Beiser, AS; Au, R; Himali, JJ; Debette, S; Pikula, A; DeCarli, C; Wolf, PA; Vasan, RS; Robins, SJ; Seshadri, S,期刊：Neurology, 页码：658-664 , 文章类型： Article，,卷期：2012年78-9]
- Objective: Higher dietary intake and circulating levels of docosahexaenoic acid (DHA) and eicosapentaenoic acid (EPA) have been related to a reduced risk for dementia, but the pathways underlying this association remain ...
- Epileptic seizures at initial presentation in patients with brain arteriovenous malformation
[作者：Garcin, B; Houdart, E; Porcher, R; Manchon, E; Saint-Maurice, JP; Bresson, D; Stapf, C,期刊：Neurology, 页码：626-631 , 文章类型： Article，,卷期：2012年78-9]
- Objectives: Brain arteriovenous malformations (AVMs) often present with epileptic seizures, but prospective data on the risk of seizures with respect to morphologic AVM characteristics are scarce. Methods: We studied 155...
- Serologic diagnosis of NMO A multicenter comparison of aquaporin-4-IgG assays
[作者：Waters, PJ; McKeon, A; Leite, MI; Rajasekharan, S; Lennon, VA; Villalobos, A; Palace, J; Mandrekar, JN; Vincent, A; Bar-Or, A; Pittock, SJ,期刊：Neurology, 页码：665-671 , 文章类型： Article，,卷期：2012年78-9]
- Objectives: Neuromyelitis optica (NMO) immunoglobulin G (IgG) (aquaporin-4 [AQP4] IgG) is highly specific for NMO and related disorders, and autoantibody detection has become an essential investigation in patients with d...
- Adult cases of mitochondrial DNA depletion due to TK2 defect An expanding spectrum
[作者：Behin, A; Jardel, C; Claeys, KG; Fagart, J; Louha, M; Romero, NB; Laforet, P; Eymard, B; Lombes, A,期刊：Neurology, 页码：644-648 , 文章类型： Article，,卷期：2012年78-9]
- Objective: In this study we aim to demonstrate the occurrence of adult forms of TK2 mutations causing progressive mitochondrial myopathy with significant muscle mitochondrial DNA (mtDNA) depletion. Methods: Patients' inv...
- Long-term survival after liver transplantation in patients with familial amyloid polyneuropathy
[作者：Yamashita, T; Ando, Y; Okamoto, S; Misumi, Y; Hirahara, T; Ueda, M; Obayashi, K; Nakamura, M; Jono, H; Shono, M; Asonuma, K; Inomata, Y; Uchino, M,期刊：Neurology, 页码：637-643 , 文章类型： Article，,卷期：2012年78-9]
- Objective: Familial amyloid polyneuropathy (FAP), which is a fatal disorder inherited in an autosomal dominant fashion, is characterized by systemic accumulation of polymerized transthyretin (TTR) in the peripheral nerve...
- Understanding epileptogenesis in calcified neurocysticercosis with perfusion MRI
[作者：Gupta, RK; Awasthi, R; Rathore, RKS; Verma, A; Sahoo, P; Paliwal, VK; Prasad, KN; Pandey, CM; Narayana, PA,期刊：Neurology, 页码：618-625 , 文章类型： Article，,卷期：2012年78-9]
- Objectives: Calcified cysticercus larva with perilesional abnormality is thought to be responsible for seizures in patients with neurocysticercosis (NCC). However, it is not well understood why some calcified cysts are a...
- Variant ataxia-telangiectasia presenting as primary-appearing dystonia in Canadian Mennonites
[作者：Saunders-Pullman, R; Raymond, D; Stoessl, AJ; Hobson, D; Nakamura, T; Pullman, S; Lefton, D; Okun, MS; Uitti, R; Sachdev, R; Stanley, K; San Luciano, M; Hagenah, J; Gatti, R; Ozelius, LJ; Bressman, SB,期刊：Neurology, 页码：649-657 , 文章类型： Article，,卷期：2012年78-9]
- Objective: To compare the phenotype of primary-appearing dystonia due to variant ataxia-telangiectasia (A-T) with that of other dystonia ascertained for genetics research. Methods: Movement disorder specialists examined ...
- Fingolimod-associated macular edema Incidence, detection, and management
[作者：Jain, N; Bhatti, MT,期刊：Neurology, 页码：672-680 , 文章类型： Review，,卷期：2012年78-9]
- Fingolimod (FTY-720), a sphingosine-1-phosphate receptor modulator, is the first US Food and Drug Administration (FDA)-approved oral agent for the treatment of relapsing forms of multiple sclerosis (MS). Two recent phase...
|