|The risk of recurrent deep venous thrombosis among heterozygous carriers of both factor V Leiden and the G20210A prothrombin mutation|
V De Stefano, I Martinelli, PM Mannucci, K Paciaroni, P Chiusolo, ...
New England Journal of Medicine 341 (11), 801-806, 1999
|Prothrombin G20210A mutant genotype is a risk factor for cerebrovascular ischemic disease in young patients|
V De Stefano, P Chiusolo, K Paciaroni, I Casorelli, E Rossi, M Molinari, ...
Blood, The Journal of the American Society of Hematology 91 (10), 3562-3565, 1998
|Preponderance of methylenetetrahydrofolate reductase C677T homozygosity among leukemia patients intolerant to methotrexate|
P Chiusolo, G Reddiconto, I Casorelli, L Laurenti, F Sora, L Mele, ...
Annals of oncology 13 (12), 1915-1918, 2002
|The risk of recurrent venous thromboembolism among heterozygous carriers of the G20210A prothrombin gene mutation|
V De Stefano, I Martinelli, PM Mannucci, K Paciaroni, E Rossi, P Chiusolo, ...
British journal of haematology 113 (3), 630-635, 2001
|Hyperhomocysteinemia and prevalence of polymorphisms of homocysteine metabolism-related enzymes in patients with inflammatory bowel disease|
A Papa, V De Stefano, S Danese, P Chiusolo, S Persichilli, I Casorelli, ...
The American journal of gastroenterology 96 (9), 2677-2682, 2001
|Mismatch repair and response to DNA-damaging antitumour therapies|
M Bignami, I Casorelli, P Karran
European journal of cancer 39 (15), 2142-2149, 2003
|Interaction between hyperhomocysteinemia and inherited thrombophilic factors in venous thromboembolism|
V DE STEFANO, IDA Casorelli, E Rossi, B Zappacosta, G Leone
Seminars in thrombosis and hemostasis 26 (03), 305-312, 2000
|Prevalence of mild hyperhomocysteinaemia and association with thrombophilic genotypes (factor V Leiden and prothrombin G20210A) in Italian patients with venous thromboembolic …|
V De Stefano, B Zappacosta, S Persichilli, E Rossi, I Casorelli, ...
British journal of haematology 106 (2), 564-568, 1999
|Drug treatment in the development of mismatch repair defective acute leukemia and myelodysplastic syndrome|
I Casorelli, J Offman, L Mele, L Pagano, S Sica, M D’Errico, G Giannini, ...
DNA repair 2 (5), 547-559, 2003
|Role of mismatch repair and MGMT in response to anticancer therapies|
I Casorelli, MT Russo, M Bignami
Anti-Cancer Agents in Medicinal Chemistry (Formerly Current Medicinal …, 2008
|Increased prevalence of the G20210A prothrombin gene variant in acute coronary syndromes without metabolic or acquired risk factors or with limited extent of disease|
F Burzotta, K Paciaroni, V De Stefano, P Chiusolo, A Manzoli, I Casorelli, ...
European heart journal 23 (1), 26-30, 2002
|Role of MUTYH and MSH2 in the control of oxidative DNA damage, genetic instability, and tumorigenesis|
MT Russo, G De Luca, I Casorelli, P Degan, S Molatore, F Barone, ...
Cancer research 69 (10), 4372-4379, 2009
|Prevalence of factor V Leiden and the G20210A prothrombin-gene mutation in inflammatory bowel disease|
A Papa, V De Stefano, A Gasbarrini, P Chiusolo, R Cianci, I Casorelli, ...
Blood coagulation & fibrinolysis 11 (5), 499-503, 2000
|The C807T/G873A polymorphism in the platelet glycoprotein Ia gene and the risk of acute coronary syndrome in the Italian population|
I Casorelli, V De Stefano, AM Leone, P Chiusolo, F Burzotta, K Paciaroni, ...
British journal of haematology 114 (1), 150-154, 2001
|DNA damage and repair in human cancer: molecular mechanisms and contribution to therapy-related leukemias|
I Casorelli, C Bossa, M Bignami
International journal of environmental research and public health 9 (8 …, 2012
|Acute lymphoblastic leukemia in the elderly. A twelve-year retrospective, single center study|
L Pagano, L Mele, I Casorelli, L Fianchi, A Di Febo, G Leone
Haematologica 85 (12), 1327-1329, 2000
|Repeated sequences in CASPASE-5 and FANCD2 but not NF1 are targets for mutation in microsatellite-unstable acute leukemia/myelodysplastic syndrome|
J Offman, K Gascoigne, F Bristow, P Macpherson, M Bignami, I Casorelli, ...
Molecular cancer research 3 (5), 251-260, 2005
|Prevalence of the factor II G20210A mutation in symptomatic patients with inherited thrombophilia|
V De Stefano, P Chiusolo, K Paciaroni, I Casorelli, A Di Mario, E Rossi, ...
Thrombosis and haemostasis 80 (08), 342-343, 1998
|Prevalence of the 677C to T mutation in the methylenetetrahydrofolate reductase gene in Italian patients with venous thrombotic disease|
V De Stefano, P Chiusolo, K Paciaroni, FG Serra, MT Voso, I Casorelli, ...
Thrombosis and haemostasis 79 (03), 686-687, 1998
|Intratumoral injection of IFN-alpha dendritic cells after dacarbazine activates anti-tumor immunity: results from a phase I trial in advanced melanoma|
C Rozera, GA Cappellini, G D’Agostino, L Santodonato, L Castiello, ...
Journal of Translational Medicine 13 (1), 139, 2015