Gong H, Tang Z, Yang Y, Sun L, Zhang W, Wang W, Cui B, Ning G. A patient with pseudohypoaldosteronism type II caused by a novel mutation in WNK4 gene. Endocrine. 2008 Jun;33(3):230-4.
Wang S, Mao C, Zhao Z, Gu Q, Jin M, Xiao Y, Jiang X, Zhao Y, Zhang Y, Ning G. Increased TTS abrogates IDO-mediated CD4(+) T cells suppression in patients with Graves' disease. Endocrine. 2009 Aug;36(1):119-25.
Zhang YW, Jia HY, Hong J, Ge Y, Zhang HJ, Shen CF, Ye L, Cui B, Li XY, Gu WQ, Zhang YF, Wang WQ, Ning G. Clinical and genetic analysis for four Chinese families with Prader-Willi syndrome. Endocrine. 2009 Aug;36(1):37-44. 我们总结下来,用基础研究的方法做临床,就基本没问题。
审稿速度:2.0 | 投稿命中率:50.0
经验分享:在投
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投稿命中率:25.0
经验分享:在投
0
求该期刊的参考文献格式,谢谢!
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偏重的研究方向:甲状腺
经验分享:2024.1.25 editor appointed
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审稿速度:3.0 | 投稿命中率:50.0
偏重的研究方向:内分泌
经验分享:感觉主编权力挺大的,人也很好,不刁钻
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我现在已经投稿了快60天,一直显示Under Review,老天啊
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这个杂志分数不高,老板与主编还认识,几乎成为我们的实验室专业户了。
Gong H, Tang Z, Yang Y, Sun L, Zhang W, Wang W, Cui B, Ning G. A patient with pseudohypoaldosteronism type II caused by a novel mutation in WNK4 gene. Endocrine. 2008 Jun;33(3):230-4.
Wang S, Mao C, Zhao Z, Gu Q, Jin M, Xiao Y, Jiang X, Zhao Y, Zhang Y, Ning G. Increased TTS abrogates IDO-mediated CD4(+) T cells suppression in patients with Graves' disease. Endocrine. 2009 Aug;36(1):119-25.
Zhang YW, Jia HY, Hong J, Ge Y, Zhang HJ, Shen CF, Ye L, Cui B, Li XY, Gu WQ, Zhang YF, Wang WQ, Ning G. Clinical and genetic analysis for four Chinese families with Prader-Willi syndrome. Endocrine. 2009 Aug;36(1):37-44.
我们总结下来,用基础研究的方法做临床,就基本没问题。
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请教下各位大牛,这个杂志接受case report吗
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审稿速度:1.0 | 投稿命中率:50.0
经验分享:5.29投稿,6.28大修,8.31修回(返修时因为拖延耽误了点时间),10.3接受,编辑和审稿人都很友好
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虽然没被接收,但仍然要给这个杂志一个好评,审稿速度快,而且就算拒稿也会给出建设性意见,推荐~
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