ida casorelli
ida casorelli
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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
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