WPRIM Management System> DCMS> Chinese Journal of Neurology> 2009> 42> 4

Volume: 42 Issue: 4

1. Executive function and working memory of patients with mild cognitive impairment Page:237—240
2. Transient white matter lesions in X-linked Charcot-Marie-Tooth disease type 1 with novel I20T mutation of gap junction protein beta 1 gene Page:241—244
3. Multiple infarcts in the posterior circulation: infarcts distribution, vascular malformation and prognosis Page:229—232
4. Mutation and polymorphism analysis of SPG4 and SPG3A in Chinese patients with hereditary spastic paraplegia Page:253—257
5. Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes/Leigh overlap syndrome caused by mutation of mitochondrial DNA G13513A Page:248—252
6. Investigation of survival motor neuron gene deletion in Chinese patients with sporadic amyotrophic lateral sclerosis Page:245—247
7. Correlation between matrix metailoprotelnase-3 polymorphism and the stability of carotid plaque Page:233—236
8. Multicenter randomized, double-blind, placebo-controlled trial of zonisamide as add-on therapy in patients with refractor partial seizures Page:263—267
9. Multicenter controlled randomized clinical trial of akatinol memantine for treatment of Aizheimer's disease Page:268—272
10. Role of autophagy and proteasome degradation pathways in apoptosis of PC12 cells transfected with A53T α-synuclein Page:258—262

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