Influence of the JAK2 V617F Mutation and Inherited Thrombophilia on the Thrombotic Risk among Patients with Myeloproliferative Disorders

BACKGROUND: A number of studies showed that the JAK2 V617F mutation increases the thrombotic risk in patients with myeloproliferative disorders (MPN) while others did not reveal this correlation, and it is unknown whether inherited thrombophilia is an additive risk factor in mutated subjects. Our ai...

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Vydáno v:Maedica (Bucur)
Hlavní autoři: TEVET, Mihaela, IONESCU, Razvan, DRAGAN, Cornel, LUPU, Anca Roxana
Médium: Artigo
Jazyk:Inglês
Vydáno: Media Med Publicis 2015
Témata:
Original Papers
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4496761/
https://ncbi.nlm.nih.gov/pubmed/26225146
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