- Transcranial brain sonography findings predict disease progression in multiple sclerosis
[作者：Walter, U; Wagner, S; Horowski, S; Benecke, R; Zettl, UK,期刊：Neurology, 页码：1010-1017 , 文章类型： Article，,卷期：2009年73-13]
- Objective: In multiple sclerosis (MS), an early neurodegenerative affection of subcortical gray matter has been suggested. Transcranial sonography (TCS) shows hyperechogenic lesions of substantia nigra (SN) and basal gan...
- Apolipoprotein genotype does not influence MS severity, cognition, or brain atrophy
[作者：van der Walt, A; Stankovich, J; Bahlo, M; Taylor, BV; van der Mei, IAF; Foote, SJ; Kilpatrick, TJ; Rubio, JP; Butzkueven, H,期刊：Neurology, 页码：1018-1025 , 文章类型： Article，,卷期：2009年73-13]
- Background: The influence of APOE allelic heterogeneity on multiple sclerosis (MS) disease severity has been reported in multiple datasets with conflicting results. Several studies have reported an unfavorable associatio...
- Increased neuronal proliferation in human bacterial meningitis
[作者：Gerber, J; Tauber, SC; Armbrecht, I; Schmidt, H; Bruck, W; Nau, R,期刊：Neurology, 页码：1026-1032 , 文章类型： Article，,卷期：2009年73-13]
- Objective: Neurogenesis is increased in experimental models of bacterial meningitis. In this study, neurogenesis was examined after bacterial infection of the CNS, and after stroke and brain trauma in humans.Methods: Bra...
- Bilateral reorganization of the dentate gyrus in hippocampal sclerosis A postmortem study
[作者：Thom, M; Martinian, L; Catarino, C; Yogarajah, M; Koepp, MJ; Caboclo, L; Sisodiya, SM,期刊：Neurology, 页码：1033-1040 , 文章类型： Article，,卷期：2009年73-13]
- Background: Hippocampal sclerosis (HS) is the most common surgical pathology associated with mesial temporal lobe epilepsy (MTLE). HS is typically characterized by mossy fiber sprouting (MFS) and reorganization of neurop...
- De novo mutations of voltage-gated sodium channel alpha(II) gene SCN2A in intractable epilepsies
[作者：Ogiwara, I; Ito, K; Sawaishi, Y; Osaka, H; Mazaki, E; Inoue, I; Montal, M; Hashikawa, T; Shike, T; Fujiwara, T; Inoue, Y; Kaneda, M; Yamakawa, K,期刊：Neurology, 页码：1046-1053 , 文章类型： Article，,卷期：2009年73-13]
- Background: Mutations of voltage-gated sodium channel alpha(II) gene, SCN2A, have been described in a wide spectrum of epilepsies. While inherited SCN2A mutations have been identified in multiple mild epilepsy cases, a d...
- Atrophy patterns in IVS10+16, IVS10+3, N279K, S305N, P301L, and V337M MAPT mutations
[作者：Whitwell, JL; Jack, CR; Boeve, BF; Senjem, ML; Baker, M; Ivnik, RJ; Knopman, DS; Wszolek, ZK; Petersen, RC; Rademakers, R; Josephs, KA,期刊：Neurology, 页码：1058-1065 , 文章类型： Article，,卷期：2009年73-13]
- Objective: To use a case-control study to assess and compare patterns of gray matter loss across groups of subjects with different mutations in the microtubule-associated protein tau (MAPT) gene.Methods: We identified al...
- Good clinical outcome after ischemic stroke with successful revascularization is time-dependent
[作者：Khatri, P; Abruzzo, T; Yeatts, SD; Nichols, C; Broderick, JP; Tomsick, TA,期刊：Neurology, 页码：1066-1072 , 文章类型： Article，,卷期：2009年73-13]
- Background: Trials of IV recombinant tissue plasminogen activator (rt-PA) have demonstrated that longer times from ischemic stroke symptom onset to initiation of treatment are associated with progressively lower likeliho...
- Child Neurology: Dravet syndrome When to suspect the diagnosis
[作者：Millichap, JJ; Koh, S; Laux, LC; Nordli, DR,期刊：Neurology, 页码：e59-e62 , 文章类型： Article，,卷期：2009年73-13]
- Dravet syndrome (DS), previously known as severe myoclonic epilepsy in infancy (SMEI), is an epileptic encephalopathy that presents with prolonged seizures in the first year of life. The seizures often occur with fever o...
|