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Increased risk of recurrent thrombosis in patients with essential thrombocythemia carrying the homozygous JAK2 V617F mutation.
De Stefano V, Za T, Rossi E, Vannucchi AM, Ruggeri M, Elli E, Micò C, Tieghi A, Cacciola RR, Santoro C, Vianelli N, Guglielmelli P, Pieri L, Scognamiglio F, Cacciola E, Rodeghiero F, Pogliani EM, Finazzi G, Gugliotta L, Leone G, Barbui T; GIMEMA Chronic Myeloproliferative Neoplasms Working Party. De Stefano V, et al. Among authors: finazzi g. Ann Hematol. 2010 Feb;89(2):141-6. doi: 10.1007/s00277-009-0788-5. Epub 2009 Jul 7. Ann Hematol. 2010. PMID: 19582452
[Congenital deficiency of antithrombin III].
Finazzi G, Barbui T. Finazzi G, et al. Haematologica. 1990 Mar-Apr;75 Suppl 2:6-13. Haematologica. 1990. PMID: 2201606 Review. Italian. No abstract available.
373 results