ClinicalJAK2V617F mutation testing: Limited utility for general hospital patients with venous and arterial thromboses in common locations
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajh.21159/fullpdf
Reference6 articles.
1. The JAK2 V617F mutation frequently occurs in patients with portal and mesenteric venous thrombosis
2. Prevalence of the Activating JAK2 Tyrosine Kinase Mutation V617F in the Budd–Chiari Syndrome
3. The V617F mutation of JAK2 is very uncommon in patients with thrombosis
4. JAK2V617F prevalence and allele burden in non-splanchnic venous thrombosis in the absence of overt myeloproliferative disorder
5. JAK2V617F is infrequently associated with arterial stroke in the absence of overt myeloproliferative disorder
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. JAK2V617Fmutation is highly prevalent in patients with ischemic stroke: a case-control study;Blood Advances;2023-09-29
2. Meta-analysis: the significance of screening for JAK2V617F mutation in Budd-Chiari syndrome and portal venous system thrombosis;Alimentary Pharmacology & Therapeutics;2011-03-13
3. JAK2V617F mutation in patients with thrombosis: to screen or not to screen?;International Journal of Laboratory Hematology;2010-12-01
4. JAK2V617F mutation for the early diagnosis of Ph− myeloproliferative neoplasms in patients with venous thromboembolism: a meta-analysis;Blood;2009-05-28
5. JAK2V617F mutation in patients with arterial thrombosis in the absence of overt myeloproliferative disease;Journal of Thrombosis and Haemostasis;2009-04
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