| 缩写名/全名 |
J INHERIT METAB DIS
JOURNAL OF INHERITED METABOLIC DISEASE |
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| ISSN号 | 0141-8955 | ||||||||||||||||||||
| 研究方向 | 医学-内分泌学与代谢 | ||||||||||||||||||||
| 影响因子 | 2015:3.541, 2016:3.97, 2017:4.092, 2018:4.287, 2019:4.036, | ||||||||||||||||||||
| 出版国家 | NETHERLANDS | ||||||||||||||||||||
| 出版周期 | Bimonthly | ||||||||||||||||||||
| 年文章数 | 108 | ||||||||||||||||||||
| 出版年份 | 1978 | ||||||||||||||||||||
| 是否OA | No | ||||||||||||||||||||
| 审稿周期(仅供参考) | 偏慢,4-8周 |
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| 录用比例 | 一般 | ||||||||||||||||||||
| 投稿链接 | https://www.editorialmanager.com/boli/default.aspx | ||||||||||||||||||||
| 投稿官网 | http://www.springer.com/medicine/internal/journal/10545 | ||||||||||||||||||||
| h-index | 91 | ||||||||||||||||||||
| CiteScore |
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| PubMed Central (PMC)链接 | http://www.ncbi.nlm.nih.gov/nlmcatalog?term=0141-8955%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. | AMP-activated protein kinase activation in mediating phenylalanine-induced neurotoxicity in experimental models of phenylketonuria Author: Lihua Lu, Xiaoming Ben, Lingling Xiao, Min Peng, Yongjun Zhang Journal: JOURNAL OF INHERITED METABOLIC DISEASE, 2017, Vol.41, 679-687, DOI:10.1007/s10545-017-0115-6 DOI |
| 2. | Demographics, diagnosis and treatment of 256 patients with tetrahydrobiopterin deficiency in mainland China: results of a retrospective, multicentre study Author: Jun Ye, Yanling Yang, Weimin Yu, Hui Zou, Jianhui Jiang, Rulai Yang, Sunny Shang, Xuefan Gu Journal: JOURNAL OF INHERITED METABOLIC DISEASE, 2012, Vol.36, 893-901, DOI:10.1007/s10545-012-9550-6 DOI |
| 3. | Clinical features and <Emphasis Type="Italic">ETFDH</Emphasis> mutation spectrum in a cohort of 90 Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency Author: Jianying Xi, Bing Wen, Jie Lin, Wenhua Zhu, Sushan Luo, Chongbo Zhao, Duoling Li, Pengfei Lin, Jiahong Lu, Chuanzhu Yan Journal: JOURNAL OF INHERITED METABOLIC DISEASE, 2013, Vol.37, 399-404, DOI:10.1007/s10545-013-9671-6 DOI |
| 4. | Hypervalinemia and hyperleucine-isoleucinemia caused by mutations in the branched-chain-amino-acid aminotransferase gene Author: X. L. Wang, C. J. Li, Y. Xing, Y. H. Yang, J. P. Jia Journal: JOURNAL OF INHERITED METABOLIC DISEASE, 2015, Vol.38, 855-861, DOI:10.1007/s10545-015-9814-z DOI |
| 5. | Household financial burden of phenylketonuria and its impact on treatment in China: a cross-sectional study Author: Lin Wang, Hui Zou, Fang Ye, Kundi Wang, Xiaowen Li, Zhihua Chen, Jie Chen, Bingjuan Han, Weimin Yu, Chun He, Ming Shen Journal: JOURNAL OF INHERITED METABOLIC DISEASE, 2016, Vol.40, 369-376, DOI:10.1007/s10545-016-9995-0 DOI |
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