JAK2V617F is infrequently associated with arterial stroke in the absence of overt myeloproliferative disorder
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1538-7836.2007.02616.x/fullpdf
Reference11 articles.
1. Thrombosis and haemorrhage in polycythaemia vera and essential thrombocythaemia
2. Definition of subtypes of essential thrombocythaemia and relation to polycythaemia vera based on JAK2 V617F mutation status: a prospective study
3. Prevalence of the Activating JAK2 Tyrosine Kinase Mutation V617F in the Budd–Chiari Syndrome
4. Latent myeloproliferative disorder revealed by the JAK2-V617F mutation and endogenous megakaryocytic colonies in patients with splanchnic vein thrombosis
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1. JAK2V617Fmutation is highly prevalent in patients with ischemic stroke: a case-control study;Blood Advances;2023-09-29
2. JAK 2 positive myeloproliferative neoplasm presenting as stroke, recurrent TIA and isolated third nerve palsy;BMJ Case Reports;2021-06
3. Enhanced Risk for Specific Somatic Myeloproliferative Neoplastic Mutations in Patients with Stroke;Current Neurovascular Research;2017-08-25
4. Cerebrovascular events as presenting manifestations of Myeloproliferative Neoplasm;Revue Neurologique;2016-11
5. Transient Ischemic Attacks as the First Presentation of JAK2-V617F Positive Chronic Myeloproliferative Neoplasm;Hematology Reports;2012-06-29
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