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浏览/检索结果: 共5条，第1-5条 帮助 已选(0)清除 条数/页：5101520253035404550556065707580859095100   排序方式：请选择作者升序作者降序题名升序题名降序发表日期升序发表日期降序提交时间升序提交时间降序 Vascular Ehlers-Danlos Syndrome With a Novel Missense COL3A1 Mutation Present With Pulmonary Complications and Iliac Arterial Dissection 期刊论文 2018, 卷号: 52, 期号: 2, 页码: 138-142 作者:  Gu, Guangchao;  Yang, Hang;  Cui, Lijia;  Fu, Yuanyuan;  Li, Fangda 收藏  |  浏览/下载：4/0  |  提交时间：2020/01/03 Ehlers-Danlos syndrome type IV  arterial dissection  pulmonary cyst  COL3A1   Systemic Multiple Aneurysms Caused by Vascular Ehlers-Danlos Syndrome 期刊论文 2016, 卷号: 50, 期号: 5, 页码: 354-8 作者:  Gui Xinyu;  Li Fangda;  Wu Lingeer;  Zheng Yuehong 收藏  |  浏览/下载：2/0  |  提交时间：2020/01/04 Ehlers-Danlos syndrome  intraperitoneal hemorrhage  systemic multiple aneurysms  vascular EDS   T in COL1A1 may cause mild osteogenesis imperfecta/Ehlers-Danlos syndrome in a Chinese family">Heterozygous mutation of c.3521C>T in COL1A1 may cause mild osteogenesis imperfecta/Ehlers-Danlos syndrome in a Chinese family 期刊论文 Intractable and Rare Diseases Research, 2015, 卷号: 4, 期号: 1, 页码: 49-53 作者:  Shi X.;  Lu Y.;  Wang Y.;  Zhang Y.-A.;  Teng Y. 收藏  |  浏览/下载：9/0  |  提交时间：2019/12/17 Ehlers-Danlos syndrome  In silico prediction  Mutations  Osteogenesis imperfecta  Type I collagen   T in COL1A1 may cause mild osteogenesis imperfecta/Ehlers-Danlos syndrome in a Chinese family."> Heterozygous mutation of c.3521C>T in COL1A1 may cause mild osteogenesis imperfecta/Ehlers-Danlos syndrome in a Chinese family. 期刊论文 Intractable & rare diseases research, 2015, 卷号: 4, 期号: 1 作者:  Shi, Xianlong;  Lu, Yanqin;  Wang, Yanzhou;  Zhang, Yu-Ang;  Teng, Yuanwei 收藏  |  浏览/下载：3/0  |  提交时间：2019/12/17 Endovascular Treatment of Bilateral Multiple Carotid-Cavernous Fistulas in a Patient with Ehlers-Danlos Syndrome 期刊论文 JOURNAL OF NEUROLOGICAL SURGERY PART A-CENTRAL EUROPEAN NEUROSURGERY, 2013, 卷号: 74 作者:  Wang, Qihong;  Chen, Gong 收藏  |  浏览/下载：1/0  |  提交时间：2019/12/19 minimal invasive  Ehlers-Danlos syndrome  endovascular treatment  caroticocavernous fistula