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Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|October 1, 1988
Keeping up with the cancer literature--PDQ ACCESSD J Perry, E M Sloane, S M Hubbard, et al.
Annals of Surgical Oncology|July 18, 2001
Survival after induction chemotherapy and surgical resection for high-grade soft tissue sarcoma. Is radiation necessary?R M Henshaw, D A Priebat, D J Perry, et al.
Journal of Thrombosis and Haemostasis : JTH|January 7, 2005
Structural interpretation of 42 mutations causing factor XI deficiency using homology modelingN M O'Connell, R E Saunders, C A Lee, et al.
Cancer|December 1, 1988
Cisplatin and mitoguazone. An induction chemotherapy regimen in advanced head and neck cancerA A Forastiere, D J Perry, G T Wolf, et al.
Blood|December 12, 2001
Congenital afibrinogenemia: mutations leading to premature termination codons in fibrinogen A alpha-chain gene are not associated with the decay of the mutant mRNAsR Asselta, S Duga, S Spena, et al.
Journal of Thrombosis and Haemostasis : JTH|July 15, 2010
The association of factor V Leiden with myocardial infarction is replicated in 1880 patients with premature diseaseP M Mannucci, R Asselta, S Duga, et al.
The British Journal of Surgery|June 12, 2013
Raised haematocrit concentration and the risk of death and vascular complications after major surgeryK M Musallam, J B Porter, P M Sfeir, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|August 23, 2011
Efficacy of prophylaxis and genotype-phenotype correlation in patients with severe Factor X deficiency in IranM Karimi, A Vafafar, S Haghpanah, et al.
Journal of Thrombosis and Haemostasis : JTH|April 30, 2013
A synonymous (c.3390C>T) or a splice-site (c.3380-2A>G) mutation causes exon 26 skipping in four patients with von Willebrand disease (2A/IIE)M T Pagliari, L Baronciani, I Garcìa Oya, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|October 1, 1996
Low thrombosis rate seen in blood donors and their relatives with inherited deficiencies of antithrombin and protein C: correlation with type of defect, family history, and absence of the factor V Leiden mutationM McColl, R C Tait, I D Walker, et al.
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