JAK2 V617F mutational frequency in essential thrombocythemia associated with splanchnic or cerebral vein thrombosis

Etiology, Management, and Outcome of the Budd-Chiari Syndrome

(2013) Sarwa Darwish Murad   ANNALS OF INTERNAL MEDICINE

Rare thromboses of cerebral, splanchnic and upper-extremity veins

(2010) Valerio De Stefano et al.   THROMBOSIS AND HAEMOSTASIS

JAK2V617F mutation for the early diagnosis of Ph- myeloproliferative neoplasms in patients with venous thromboembolism: a meta-analysis

(2009) F. Dentali et al.   BLOOD

The presence of JAK2V617F mutation in the liver endothelial cells of patients with Budd-Chiari syndrome

(2009) S. Sozer et al.   BLOOD

JAK2V617F Mutation Associated with Cerebral Venous Thrombosis: A Report of Five Cases

(2009) G. Godeneche et al.   CEREBROVASCULAR DISEASES

Influence of the JAK2 V617F mutation and inherited thrombophilia on the thrombotic risk among patients with essential thrombocythemia

(2009) V. De Stefano et al.   HAEMATOLOGICA

JAK2-V617F mutation in cerebral venous thrombosis

(2009) K. KOOPMAN et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

Association of V617F Jak2 mutation with the risk of thrombosis among patients with essential thrombocythaemia or idiopathic myelofibrosis: A systematic review

(2009) Federico Lussana et al.   THROMBOSIS RESEARCH

Absence of the JAK2 exon 12 mutations in patients with splanchnic venous thrombosis and without overt myeloproliferative neoplasms

(2008) Alessia Fiorini et al.   AMERICAN JOURNAL OF HEMATOLOGY

The impact of JAK2 and MPL mutations on diagnosis and prognosis of splanchnic vein thrombosis: a report on 241 cases

(2008) J.-J. Kiladjian et al.   BLOOD

Prevalence of theJAK2V617F mutation in patients with unprovoked venous thromboembolism of common sites and without overt myeloproliferative neoplasms

(2008) Tommaso Za et al.   BRITISH JOURNAL OF HAEMATOLOGY

Effect of JAK2 V617F on thrombotic risk in patients with essential thrombocythemia: measuring the uncertain

(2008) P. D. Ziakas   HAEMATOLOGICA

Is JAK2 V617F mutation more than a diagnostic index?

(2008) Issa J. Dahabreh et al.   LEUKEMIA RESEARCH