WPRIM Management System> DCMS> Chinese Journal of Neurology> 2019> 52> 6

Volume: 52 Issue: 6

1. Paying attention to the study of proteomics in muscular diseases Page:441—445
2. The correlation of the levels of interleukin-15 with late onset myasthenia gravis Page:446—451
3. Needle electromyography of the genioglossus muscle in the detection of amyotrophic lateral sclerosis Page:452—456
4. Paramyotonia congenita and hypokalemic periodic paralysis in a family with mutation p.R1448H in α-subunit type Ⅳ of voltage gated sodium channel gene Page:457—462
5. Effects of cardiac function and renal function on early neurological function recovery in patients with acute stroke Page:463—471
6. The role of intravenous thrombolysis in the endovascular treatment of acute anterior circulation vascular occlusive stroke Page:472—477
7. Pedigree study of hereditary small cerebral vascular disease caused by c.821G＞A heterozygous mutation of HtrA serine protease-1 gene Page:478—486
8. Clinical analysis of four cases of KCNQ2 gene-related neonatal-infantile epilepsy Page:487—492
9. Clinical and aspartoacylase gene mutation analysis of Canavan disease in a child Page:493—497
10. Dystrophinopathy Page:498—506
11. Progress of disturbances in energy metabolism in amyotrophic lateral sclerosis Page:507—509
12. Clinical application of assessment scales related to Charcot-Marie-Tooth disease Page:510—515
13. Research progresses on the role of metal ions in the pathogenesis of Parkinson's disease Page:516—520

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