全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...
-  2018 

有汗性外胚叶发育不良合并系统性红斑狼疮1例

DOI: 10.6040/j.issn.1671-7554.0.2017.273

Keywords: 系统性红斑狼疮,有汗性外胚叶发育不良,

Full-Text   Cite this paper   Add to My Lib

Abstract:

References

[1]  Lee JR, White TW. Connexin-26 mutations in deafness and skin disease[J]. Expert Rev Mol Med, 2009, 19(11):35.
[2]  赵蓓,陈学军,周夕湲,等.应用外显子测序技术查找有汗性外胚叶发育不良综合征家系致病基因[J]. 中国皮肤性病学杂志,2017,31(9):16-20.
[3]  Kiani AN, Magder LS, Post WS, et al. Coronary calcification in SLE:comparison with the multi-ethnic study of atherosclerosis[J].Rheumatology(Oxford), 2015, 54(11):1976-1981.
[4]  Torrente-segarra V, Salman-monte TC, Rua-figueroa I, et al. Fibromyalgia prevalence and related factors in a large registry of patients with systemic lupus erythematosus[J]. Clin Exp Rheumatol, 2016, 34(Suppl 2):40-47.
[5]  刘丽,高阳,李亚男. 儿童有汗性外胚层发育不良合并银屑病一例[J]. 中华全科医师杂志,2015,14(11):884-885.
[6]  Van Steensel MA, Steijlen PM, Bladergroen RS, et al. A phenotype resembling the clouston syndrome with deafness is associated with a novel missens GJB2 mutation[J]. J Invest Dermatol, 2004, 123(2):291-293.
[7]  Cao L, Tong H, Xu G, et al. Systemic lupus erythematous and malignancy risk: a meta-analysis[J]. PLoS One, 2015, 10(4):122964.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133