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WPRIM Management System>
DCMS
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Chinese Journal of Neurology
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2019
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52
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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