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SCI期刊名:   期刊ISSN:   研究方向:   影响因子: -   结果排序:

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基本信息
期刊名字Orphanet Journal of Rare Diseases
ORPHANET J RARE DIS
期刊ISSN1750-1172
2011-2012最新影响因子5.074
期刊官方网站http://ojrd.biomedcentral.com
期刊投稿网址https://www.editorialmanager.com/ojrd
通讯方式BIOMED CENTRAL LTD, 236 GRAYS INN RD, FLOOR 6, LONDON, ENGLAND, WC1X 8HL
涉及的研究方向医学-医学:研究与实验
出版国家ENGLAND
出版周期Irregular
出版年份2006
中科院SCI期刊分区2 区
PubMed Central (PMC)链接http://www.ncbi.nlm.nih.gov/nlmcatalog?term=1750-1172%5BISSN%5D
平均审稿速度(网友分享经验)平均 个月的审稿周期
平均录用比例(网友分享经验)一般%
该杂志上中国学者近期发表的论文
中国学者近期发表的论文
1.Challenge in pathologic diagnosis of Alport syndrome: evidence from correction of previous misdiagnosis.

Author: Yao XD, Chen X, Huang GY, Yu YT, Xu ST, Hu YL, Wang QW, Chen HP, Zeng CH, Ji DX, Hu WX, Tang Z, Liu ZH.
Journal: Orphanet J Rare Dis. 2012 Dec 21;7:100. doi: 10.1186/1750-1172-7-100.
2.Amyloidosis cutis dyschromica.

Author: Qiao J, Fang H, Yao H.
Journal: Orphanet J Rare Dis. 2012 Dec 12;7:95. doi: 10.1186/1750-1172-7-95.
3.An epidemiological and clinical analysis of craniomaxillofacial fibrous dysplasia in a Chinese population.

Author: Cheng J, Wang Y, Yu H, Wang D, Ye J, Jiang H, Wu Y, Shen G.
Journal: Orphanet J Rare Dis. 2012 Oct 17;7:80. doi: 10.1186/1750-1172-7-80.
4.A systematic review of genetic skeletal disorders reported in Chinese biomedical journals between 1978 and 2012.

Author: Cui Y, Zhao H, Liu Z, Liu C, Luan J, Zhou X, Han J.
Journal: Orphanet J Rare Dis. 2012 Aug 22;7:55. doi: 10.1186/1750-1172-7-55.
5.ESR1, HK3 and BRSK1 gene variants are associated with both age at natural menopause and premature ovarian failure.

Author: Qin Y, Sun M, You L, Wei D, Sun J, Liang X, Zhang B, Jiang H, Xu J, Chen ZJ.
Journal: Orphanet J Rare Dis. 2012 Jan 17;7:5. doi: 10.1186/1750-1172-7-5.
6.FGFR3 gene mutation plus GRB10 gene duplication in a patient with achondroplasia plus growth delay with prenatal onset.

Author: Yuan H, Huang L, Hu X, Li Q, Sun X, Xie Y, Kong S, Wang X.
Journal: Orphanet J Rare Dis. 2016 Jul 2;11(1):89. doi: 10.1186/s13023-016-0465-4.
7.Causes of death and clinical characteristics of 34 patients with Mucopolysaccharidosis II in Taiwan from 1995-2012.

Author: Lin HY, Chuang CK, Huang YH, Tu RY, Lin FJ, Lin SJ, Chiu PC, Niu DM, Tsai FJ, Hwu WL, Chien YH, Lin JL, Chou YY, Tsai WH, Chang TM, Lin SP.
Journal: Orphanet J Rare Dis. 2016 Jun 27;11(1):85. doi: 10.1186/s13023-016-0471-6.
8.Improvement of sexual function in POEMS syndrome after combination therapy of Lenalidomide and dexamethasone.

Author: Yang H, Huang X, Cai Q, Wang C, Cao X, Zhou D, Li J.
Journal: Orphanet J Rare Dis. 2016 Jun 18;11(1):80. doi: 10.1186/s13023-016-0461-8.
9.Catastrophic expenditure and impoverishment of patients affected by 7 rare diseases in China.

Author: Xin XX, Guan XD, Shi LW.
Journal: Orphanet J Rare Dis. 2016 Jun 6;11(1):74. doi: 10.1186/s13023-016-0454-7.
10.Estimating epidemiological data of Multiple sclerosis using hospitalized data in Shandong Province, China.

Author: Liu X, Cui Y, Han J.
Journal: Orphanet J Rare Dis. 2016 Jun 4;11(1):73. doi: 10.1186/s13023-016-0457-4.
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