- Relationship between etiology and covert cognition in the minimally conscious state
[作者：Cruse, D; Chennu, S; Chatelle, C; Fernandez-Espejo, D; Bekinschtein, TA; Pickard, JD; Laureys, S; Owen, AM,期刊：Neurology, 页码：816-822 , 文章类型： Article，,卷期：2012年78-11]
- Objectives: Functional neuroimaging has shown that the absence of externally observable signs of consciousness and cognition in severely brain-injured patients does not necessarily indicate the true absence of such abili...
- SMN1 gene duplications are associated with sporadic ALS
[作者：Blauw, HM; Barnes, CP; van Vught, PWJ; van Rheenen, W; Verheul, M; Cuppen, E; Veldink, JH; van den Berg, LH,期刊：Neurology, 页码：776-780 , 文章类型： Article，,卷期：2012年78-11]
- Objective: To investigate the role of SMN1 and SMN2 copy number variation and point mutations in amyotrophic lateral sclerosis (ALS) pathogenesis in a large population. Methods: We conducted a genetic association study i...
- The LRRK2 G2019S mutation is associated with Parkinson disease and concomitant non-skin cancers
[作者：Inzelberg, R; Cohen, OS; Aharon-Peretz, J; Schlesinger, I; Gershoni-Baruch, R; Djaldetti, R; Nitsan, Z; Ephraty, L; Tunkel, O; Kozlova, E; Inzelberg, L; Kaplan, N; Mehr, TF; Mory, A; Dagan, E; Schechtman, E; Friedman, E; Hassin-Baer, S,期刊：Neurology, 页码：781-786 , 文章类型： Article，,卷期：2012年78-11]
- Objective: In view of the fact that cancer patterns in patients with Parkinson disease (PD) differ from the general population, we aimed to verify whether patients with PD with LRRK2 mutations have an increased risk for ...
- The tremor network targeted by successful VIM deep brain stimulation in humans
[作者：Klein, JC; Barbe, MT; Seifried, C; Baudrexel, S; Runge, M; Maarouf, M; Gasser, T; Hattingen, E; Liebig, T; Deichmann, R; Timmermann, L; Weise, L; Hilker, R,期刊：Neurology, 页码：787-795 , 文章类型： Article，,卷期：2012年78-11]
- Objective: Deep brain stimulation (DBS) of the ventral intermediate nucleus of thalamus (VIM) is a treatment option in medically intractable tremor, such as essential tremor or tremor-dominant Parkinson disease (PD). Alt...
- Homozygous c.14576G > A variant of RNF213 predicts early-onset and severe form of moyamoya disease
[作者：Miyatake, S; Miyake, N; Touho, H; Nishimura-Tadaki, A; Kondo, Y; Okada, I; Tsurusaki, Y; Doi, H; Sakai, H; Saitsu, H; Shimojima, K; Yamamoto, T; Higurashi, M; Kawahara, N; Kawauchi, H; Nagasaka, K; Okamoto, N; Mori, T; Koyano, S; Kuroiwa, Y; Taguri, M; Morita, S; Matsubara, Y; Kure, S; Matsumoto, N,期刊：Neurology, 页码：803-810 , 文章类型： Article，,卷期：2012年78-11]
- Objective: RNF213 was recently reported as a susceptibility gene for moyamoya disease (MMD). Our aim was to clarify the correlation between the RNF213 genotype and MMD phenotype. Methods: The entire coding region of the ...
- The evidence for a role of B cells in multiple sclerosis
[作者：Disanto, G; Morahan, JM; Barnett, MH; Giovannoni, G; Ramagopalan, SV,期刊：Neurology, 页码：823-832 , 文章类型： Review，,卷期：2012年78-11]
- Understanding the pathogenesis of complex immunologic disorders such as multiple sclerosis (MS) is challenging. Abnormalities in many different cell types are observed in the immune system and CNS of patients with MS and...
- Predictors of hemorrhage volume and disability after perimesencephalic subarachnoid hemorrhage
[作者：Naidech, AM; Rosenberg, NF; Maas, MB; Bendok, BR; Batjer, HH; Nemeth, AJ,期刊：Neurology, 页码：811-815 , 文章类型： Article，,卷期：2012年78-11]
- Objective: The determinants of subarachnoid hemorrhage (SAH) volume and an atypical pattern of blood are not clear. Our objective was to determine if reduced platelet activity on admission and abnormal venous drainage ar...
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