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Volume: Issue: 2

1. The clinical-electroencephalographic features of the 6 patients with idiopathic generalized epilepsy in adults with phantom absences Page:78—81
2. Clinical and imaging characteristics of chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids: one case report Page:95—99
3. Early diagnosis of peripheral neuropathy by corneal confocal microscopy in patients with impaired glucose tolerance Page:107—111
4. Twenty cases of cerebral venous sinus thrombosis presented as isolated intracranial hypertension Page:112—116
5. Effect of transplantation of mouse marrow stromal cells through injection into cerebrospinal fluid on Cu/Zn superoxide dismutase 1 transgenic mice Page:122—126
6. A study of disability adjusted life year about patients with epilepsy Page:87—90
7. Expressions of inositol requiring enzyme 1α mediated endoplasmic reticulum stress-associated molecules in the hippocampus of rats following status epilepsy Page:91—94
8. Identification of two survival motor neuron gene 1 gene mutations and evaluation of their effects on full-length survival motor neuron gene 1 transcripts Page:100—106
9. Research on the relationship between recurrence of cryptogenic ischemic cerebrovascular disease and patent foramen ovale Page:117—121
10. Effects of cytochrome P450 isozymes 2A6, 2B6, 2C9 and 2C19 genetic polymorphisms on plasma concentration of sodium valproate Page:82—86
11. Correlation of the levels of interleukin-17 and its receptor with myasthenia gravis Page:118—122
12. Walking ability and cognitive function changes in normal pressure hydrocephalus patients after cerebrospinal fluid tap test Page:113—117
13. Effect of mini Ad-ATP7B-GFP on the copper metabolism of skin fibroblasts of Wilson′s disease patients Page:102—107
14. Analysis of clinical and electrophysiological features in patients with hereditary neuropathy with liability to pressure palsy diagnosed by gene analysis Page:93—97
15. Analysis of electroencephalography and synchronous electrocardiography changes in non-epileptic seizures Page:123—126
16. Imaging diagnosis of congenital absence of the internal carotid artery Page:108—112
17. Mutation (Thr704Met) of the SCN4A gene causes severe familial hypokalemic periodic paralysis Page:98—101
18. Clinical, neuroimaging and genetic profiles of amyotrophic lateral sclerosis with frontotemporal lobe degeneration Page:87—92

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