Showing results (21-30 of 99) with videos related to

Sort By:
Pageof 10
Molecular Human Reproduction|June 9, 2012
The M2 haplotype in the ANXA5 gene is an independent risk factor for idiopathic small-for-gestational age newbornsG Tiscia, D Colaizzo, G Favuzzi, et al.
British Journal of Haematology|February 13, 2001
The risk of venous thromboembolism in family members with mutations in the genes of factor V or prothrombin or bothI Martinelli, P Bucciarelli, M Margaglione, et al.
Indian Journal of Human Genetics|March 20, 2010
Identification of FVIII gene mutations in patients with hemophilia A using new combinatorial sequencing by hybridizationM Chetta, A Drmanac, R Santacroce, et al.
Journal of Thrombosis and Haemostasis : JTH|December 6, 2011
Risk of obstetric and thromboembolic complications in family members of women with previous adverse obstetric outcomes carrying common inherited thombophiliasM Villani, G L Tiscia, M Margaglione, et al.
Italian Heart Journal. Supplement : Official Journal of the Italian Federation of Cardiology|April 20, 2001
[Hypersensitivity to oral anticoagulants: report of a case]M M Patella, P E Russo, D De Lucia, et al.
Ophthalmic Research|November 27, 2001
Apolipoprotein E polymorphisms in age-related macular degeneration in an Italian populationF Simonelli, M Margaglione, F Testa, et al.
Thrombosis and Haemostasis|December 8, 1998
Fibrinogen plasma levels in an apparently healthy general population--relation to environmental and genetic determinantsM Margaglione, G Cappucci, D Colaizzo, et al.
Haematologica|April 28, 2001
Familial thrombophilia and the occurrence of fetal growth restrictionP Martinelli, E Grandone, D Colaizzo, et al.
Thrombosis and Haemostasis|December 29, 2000
Genetic modulation of oral anticoagulation with warfarinM Margaglione, D Colaizzo, G D'Andrea, et al.
American Journal of Obstetrics and Gynecology|November 20, 1998
Genetic susceptibility to pregnancy-related venous thromboembolism: roles of factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutationsE Grandone, M Margaglione, D Colaizzo, et al.
Pageof 10