Falanga A, Schieppati F, Russo D.
Semin Thromb Hemost. 2015;41(7):756-64.
Pubblicazioni 2015
The mechanisms of cancer-associated thrombosis
Falanga A, Marchetti M, Russo L.
Thromb Res. 2015;135 Suppl 1:S8-S11.
Venous thromboembolism prophylaxis and treatment in patients with cancer: American Society of Clinical Oncology clinical practice guideline update
Lyman GH, Bohlke K, Falanga A; American Society of Clinical Oncology.
J Oncol Pract. 2015;11(3):e442-4.
Management of cancer-associated disseminated intravascular coagulation: guidance from the SSC of the ISTH: reply
Thachil J, Falanga A, Levi M, Liebman H, Di Nisio M.
J Thromb Haemost. 2015;13(7):1352-3.
Recurrent venous thromboembolism in anticoagulated patients with cancer: management and short-term prognosis
Schulman S, Zondag M, Linkins L, Pasca S, Cheung YW, de Sancho M, Gallus A, Lecumberri R, Molnar S, Ageno W, Le Gal G, Falanga A, Hulegårdh E, Ranta S, Kamphuisen P, Debourdeau P, Rigamonti V, Ortel TL, Lee A.
J Thromb Haemost. 2015;13(6):1010-8.
Venous thromboembolism prophylaxis and treatment in patients with cancer: american society of clinical oncology clinical practice guideline update 2014
Lyman GH, Bohlke K, Khorana AA, Kuderer NM, Lee AY, Arcelus JI, Balaban EP, Clarke JM, Flowers CR, Francis CW, Gates LE, Kakkar AK, Key NS, Levine MN, Liebman HA, Tempero MA, Wong SL, Somerfield MR, Falanga A; American Society of Clinical Oncology.
J Clin Oncol. 2015;33(6):654-6.
Management of cancer-associated disseminated intravascular coagulation: guidance from the SSC of the ISTH
Thachil J, Falanga A, Levi M, Liebman H, Di Nisio M; Scientific and Standardization Committee of the International Society on Thrombosis and Hemostasis.
J Thromb Haemost. 2015;13(4):671-5.
FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor
Peterlongo P, Catucci I, Colombo M, Caleca L, Mucaki E, Bogliolo M, Marin M, Damiola F, Bernard L, Pensotti V, Volorio S, Dall’Olio V, Meindl A, Bartram C, Sutter C, Surowy H, Sornin V, Dondon MG, Eon-Marchais S, Stoppa-Lyonnet D, Andrieu N, Sinilnikova OM; GENESIS, Mitchell G, James PA, Thompson E; kConFab; SWE-BRCA, Marchetti M, Verzeroli C, Tartari C, Capone GL, Putignano AL, Genuardi M, Medici V, Marchi I, Federico M, Tognazzo S, Matricardi L, Agata S, Dolcetti R, Della Puppa L, Cini G, Gismondi V, Viassolo V, Perfumo C, Mencarelli MA, Baldassarri M, Peissel B, Roversi G, Silvestri V, Rizzolo P, Spina F, Vivanet C, Tibiletti MG, Caligo MA, Gambino G, Tommasi S, Pilato B, Tondini C, Corna C, Bonanni B, Barile M, Osorio A, Benitez J, Balestrino L, Ottini L, Manoukian S, Pierotti MA, Renieri A, Varesco L, Couch FJ, Wang X, Devilee P, Hilbers FS, van Asperen CJ, Viel A, Montagna M, Cortesi L, Diez O, Balmaña J, Hauke J, Schmutzler RK, Papi L, Pujana MA, Lázaro C, Falanga A, Offit K, Vijai J, Campbell I, Burwinkel B, Kvist A, Ehrencrona H, Mazoyer S, Pizzamiglio S, Verderio P, Surralles J, Rogan PK, Radice P.
Hum Mol Genet. 2015;24(18):5345-55.