New advances in identifying genetic anomalies in stroke-prone probands-Reference-Cited by-同舟云学术

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New advances in identifying genetic anomalies in stroke-prone probands

Published:2003-07 Issue:4 Volume:5 Page:317-323
ISSN:1523-3804
Container-title:Current Atherosclerosis Reports
language:en
Short-container-title:Curr Atheroscler Rep

Author:

Meschia James F.,Worrall Bradford B.

Publisher

Springer Science and Business Media LLC

Subject

Cardiology and Cardiovascular Medicine

Link

http://link.springer.com/content/pdf/10.1007/s11883-003-0055-5.pdf

Reference64 articles.

1. Joutel A, Corpechot C, Ducros A, et al.: Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia. Nature 1996, 383:707–710.

2. Gretarsdottir S, Sveinbjornsdottir S, Jonsson HH, et al.: Localization of a susceptibility gene for common forms of stroke to 5q12. Am J Hum Genet 2002, 70:593–603.

3. Meschia JF, Brown RD Jr, Brott TG, et al.: The Siblings With Ischemic Stroke Study (SWISS) Protocol. BMC Med Genet 2002, 3:1.

4. Worrall BB, Chen DT, Meschia JF: Ethical and methodological issues in pedigree stroke research. Stroke 2001, 32:1242–1249.

5. Markus HS, Martin RJ, Simpson MA, et al.: Diagnostic strategies in CADASIL. Neurology 2002, 59:1134–1138.

Cited by 6 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. Molecular basis of stroke;Clinical Molecular Medicine;2020

2. Notch signaling in cerebrovascular diseases (Review);Molecular Medicine Reports;2016-08-19

3. Molecular genetics of coronary artery disease and ischemic stroke;Personalized Medicine Universe;2015-07

4. Molecular Genetics of Stroke;Colloquium Series on Genomic and Molecular Medicine;2012-03-31

5. Proinflammatory Gene Polymorphisms and Ischemic Stroke;Current Pharmaceutical Design;2008-11-01

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