Successful Endovascular Treatment of a Ruptured Superior Mesenteric Artery in a Patient with Ehlers‒Danlos Syndrome-Reference-Cited by-同舟云学术

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Successful Endovascular Treatment of a Ruptured Superior Mesenteric Artery in a Patient with Ehlers‒Danlos Syndrome

Published:2013-10 Issue:7 Volume:27 Page:975.e1-975.e5
ISSN:0890-5096
Container-title:Annals of Vascular Surgery
language:en
Short-container-title:Annals of Vascular Surgery

Author:

Yasuda Shota,Imoto Kiyotaka,Uchida Keiji,Machida Daisuke,Yanagi Hiromasa,Sugiura Tadahisa,Kurosawa Kenji,Masuda Munetaka

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine,General Medicine,Surgery

Reference16 articles.

1. Results of the Jostent coronary stentgraft implantation in various clinical settings: procedural and follow-up results;Gercken;Catherter Cardiovasc Interv,2002

2. Clinical and genetic aspects of Ehlers‒Danlos syndrome, classic type;Malfait;Genet Med,2010

3. The molecular basis of classic Ehlers‒Danlos syndrome: a comprehensive study of biochemical and molecular findings in 48 unrelated patients;Malfait;Hum Mutat,2005

4. Arterial rupture in classic Ehlers‒Danlos syndrome with COL5A1 mutation;Borck;Am J Med Genet A,2010

5. Endovascular repair of multiple infrageniculate aneurysms in a patient with vascular type Ehlers‒Danlos syndrome;Domenick;J Vasc Surg,2011

Cited by 23 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Iliac artery dissection and rupture in a patient with classic Ehlers-Danlos syndrome due to COL5A1 null variant;Journal of Vascular Surgery Cases, Innovations and Techniques;2024-06

2. Case Report: Hybrid approach as a Rescue Treatment in a patient with vascular Ehlers–Danlos Syndrome;Frontiers in Surgery;2023-10-23

3. Comprehensive genetic screening for vascular Ehlers–Danlos syndrome through an amplification‐based next‐generation sequencing system;American Journal of Medical Genetics Part A;2022-10-03

4. A patient with a novel pathogenic variant in COL5A1 exhibiting prominent vascular and cardiac features;American Journal of Medical Genetics Part A;2022-04-09

5. Clinical and molecular characteristics of 168 probands and 65 relatives with a clinical presentation of classical Ehlers–Danlos syndrome;Human Mutation;2021-07-26

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