No indication for CALR mutation analysis in Irish patients presenting with deep vein thrombosis or pulmonary embolism
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s11845-019-02018-3.pdf
Reference5 articles.
1. Martin K (2017) Risk factors for and management of MPN-associated bleeding and thrombosis. Curr Hematol Malig Rep 12:389–396
2. Bertozzi I, Peroni E, Coltro G, Bogoni G, Cosi E, Santarossa C, Fabris F, Randi ML (2016) Thrombotic risk correlates with mutational status in true essential thrombocythemia. Eur J Clin Investig 46:683–689
3. Zerjavic K, Zagradisnik B, Stangler Herodez S, Lokar L, Glaser Krasevac M, Kokalj Vokac N (2010) Is the JAK2 V617F mutation a hallmark for different forms of thrombosis? Acta Haematol 124:49–56
4. Ianotto JC, Chauveau A, Luque Paz D, Delluc A, Tromeur C, Couturier MA, Gouillou M, Berthou C, Mottier D, Ugo V (2016) Absence of CALR mutation among a cohort of 394 unselected patients with a first episode of unprovoked venous thromboembolism. Thromb Haemost 115:225–226
5. Ianotto JC, Chauveau A, Mottier D, Ugo V, Berthou C, Lippert E, Delluc A (2017) JAK2 V617F and calreticulin mutations in recurrent venous thromboembolism: results from the EDITH prospective cohort. Ann Hematol 96:383–386
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