| 缩写名/全名 |
AMYOTROPH LAT SCL FR
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration |
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| ISSN号 | 2167-8421 | ||||||||||||||||||||
| 研究方向 | CLINICAL NEUROLOGY- | ||||||||||||||||||||
| 影响因子 | 2015:2.677, 2016:3.054, 2017:2.982, 2018:2.883, 2019:3.286, | ||||||||||||||||||||
| 出版国家 | ENGLAND | ||||||||||||||||||||
| 出版周期 | |||||||||||||||||||||
| 年文章数 | 61 | ||||||||||||||||||||
| 出版年份 | 0 | ||||||||||||||||||||
| 是否OA | No | ||||||||||||||||||||
| 审稿周期(仅供参考) | |||||||||||||||||||||
| 录用比例 | |||||||||||||||||||||
| 投稿链接 | https://mc.manuscriptcentral.com/als | ||||||||||||||||||||
| 投稿官网 | http://www.tandfonline.com/loi/iafd20 | ||||||||||||||||||||
| h-index | 66 | ||||||||||||||||||||
| CiteScore |
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| PubMed Central (PMC)链接 | http://www.ncbi.nlm.nih.gov/nlmcatalog?term=2167-8421%5BISSN%5D | ||||||||||||||||||||
| 中科院SCI期刊分区 （ 2018年新版本） |
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| 中科院SCI期刊分区 （ 2020年新版本） |
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| 中国学者近期发表的论文 | |
| 1. | Associations between neuropsychiatric symptoms and cognition in Chinese patients with amyotrophic lateral sclerosis. Author: Wei Q, Chen X, Cao B, Ou R, Zhao B, Wu Y, Shang H. Journal: Amyotroph Lateral Scler Frontotemporal Degener. 2016 Jul-Aug;17(5-6):358-65. doi: 10.3109/21678421.2016.1154574. Epub 2016 Mar 10. PubMed |
| 2. | Mutations in FUS are the most frequent genetic cause in juvenile sporadic ALS patients of Chinese origin. Author: Zou ZY, Liu MS, Li XG, Cui LY. Journal: Amyotroph Lateral Scler Frontotemporal Degener. 2016 Apr-May;17(3-4):249-52. doi: 10.3109/21678421.2016.1143012. Epub 2016 Mar 14. PubMed |
| 3. | CHCHD10 is not a frequent causative gene in Chinese ALS patients. Author: Li XL, Shu S, Li XG, Liu Q, Liu F, Cui B, Liu MS, Peng B, Cui LY, Zhang X. Journal: Amyotroph Lateral Scler Frontotemporal Degener. 2016 Jul-Aug;17(5-6):458-60. doi: 10.3109/21678421.2016.1170151. Epub 2016 Apr 14. PubMed |
| 4. | Screening of the TBK1 gene in familial and sporadic amyotrophic lateral sclerosis patients of Chinese origin. Author: Shu S, Li XL, Liu Q, Liu F, Cui B, Liu MS, Cui LY, Li XG, Zhang X. Journal: Amyotroph Lateral Scler Frontotemporal Degener. 2016 Jun 3:1-3. [Epub ahead of print] PubMed |
| 5. | H46R SOD1 mutation is consistently associated with a relatively benign form of amyotrophic lateral sclerosis with slow progression. Author: Zou ZY, Liu MS, Li XG, Cui LY. Journal: Amyotroph Lateral Scler Frontotemporal Degener. 2016 Jun 27:1-4. [Epub ahead of print] PubMed |
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