Table of Contents
Editor's Note
| Editor's Note | |
| Editorial Office of Chinese Journal of Contemporary Neurology and Neurosurgery |
Special Topics
| Application of peripheral nerve and muscle ultrasound in neuromuscular diseases | |
| Ming‑sheng LIU | 771-774 |
Special Reviews
| Clinical and mechanism research progress on short tandem repeat ⁃ related neuromuscular diseases | |
| Ya‑lan WAN, Jia‑xi YU, Jian‑wen DENG, Dao‑jun HONG, Zhao‑xia WANG | 775-781 |
Neuromuscular Disease: Clinical Study
| Analysis of clinical and histopathology characteristics of asymptomatic and pauci ⁃ symptomatic hyperCKemia | |
| Yu‑jing YUAN, Chang LIU, Zhi‑ying XIE, Ya‑wen ZHAO, Ling‑chao MENG, He LÜ, Zhao‑xia WANG, Yun YUAN, Wei ZHANG | 782-788 |
| Analysis of clinical and pathological characteristics of scleromyositis patients with positive anti⁃Ku or anti⁃PM⁃Scl antibodies | |
| Xin‑yu ZHANG, Ya‑wen ZHAO, Wei ZHANG, Zhao‑xia WANG, Yun YUAN | 789-797 |
| Oculopharyngodistal myopathy caused by CGG repeat expansion in 5'untranslated region of LRP12 gene: four cases report | |
| Jia‑xi YU, Meng YU, Wei ZHANG, Yun YUAN, Jian‑wen DENG, Zhao‑xia WANG | 798-806 |
| Analysis of clinical and electrophysiological charactertics of hereditary neuropathy with liability to pressure palsies | |
| Yi LI, Yun JIANG, Jing HE, Hui‑yan YU, Xiang WANG, Yin‑hong LIU | 807-812 |
Neuromuscular Disease: Case Report
| Hereditary myopathy with early respiratory failure in China: one case report and literatures review | |
| Ying LI, Xue‑liang QI, Wei ZHANG, Li‑qun FENG, Guang‑zhi LIU, Yun YUAN | 813-820 |
| Mitochondrial myopathy presenting as acute respiratory failure: one case report | |
| Hui WANG, Meng YU, He LÜ, Wei ZHANG, Yun YUAN, Zhao‑xia WANG | 821-825 |
| Phosphoserine aminotransferase deficiency in childhood ichthyosis with adolescent peripheral neuropathy caused by PSAT1 gene mutation: one case report | |
| Ping LI, Yan‑fang XU, Shuai HU, Xiao‑xia ZENG, Xue‑liang QI | 826-831 |
| Limb ⁃ girdle muscular dystrophy with congenital myasthenic syndrome caused by GMPPB gene mutation: one case report | |
| Ran LI, Hui‑min ZOU, Chun‑ye XING, Jin SONG, Yan‑lei HAO | 832-837 |
| Perioperative rehabilitation management for a child with spinal muscular atrophy: one case report | |
| Wen‑zhu LI, Chen‑hao WANG, Zhen HUANG, Cui‑jie WEI, Hui XIONG, Bei‑yu XU, Chun‑de LI, Cheng‑li QUE | 838-843 |
Functional Neurological Disorder
| Diagnosis and treatment of functional dystonia | |
| Shu‑hua LI, Wen SU, Hai‑bo CHEN | 844-849 |
| Functional dystonia: one case report | |
| Jin‑tao WANG, Gang WANG | 850-852 |
Clinical Study
| A pedigree of early ⁃ onset familial Alzheimer's disease type 3 with spastic paraplegia as the primary manifestation | |
| Hai‑jiang LI, Chao‑dong WANG | 853-858 |
| Clinical characteristic for stroke in plateau area with altitude of 4000 meters above: 103 cases report | |
| Zhong‑zheng HE, Rui‑qian LI, Zhi‑yong LIU, Qian‑fa LONG, Shu‑yuan YUE, Yan‑ping YANG | 859-863 |
Review
| Research progress on the difference of atherosclerosis between different sexes | |
| Ya‑wei WANG, Feng TIAN | 864-871 |
This work is licensed under a Creative Commons Attribution 3.0 License.
ISSN: 1672-6731