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Journal of Thrombosis and Haemostasis : JTH|October 21, 2016
Immunochip analysis identifies novel susceptibility loci in the human leukocyte antigen region for acquired thrombotic thrombocytopenic purpuraI Mancini, I Ricaño-Ponce, E Pappalardo, et al.
Journal of Thrombosis and Haemostasis : JTH|September 1, 2018
Targeted sequencing to identify novel genetic risk factors for deep vein thrombosis: a study of 734 genesH G de Haan, A van Hylckama Vlieg, L A Lotta, et al.
Journal of Thrombosis and Haemostasis : JTH|November 27, 2014
Predictors of von Willebrand disease diagnosis in individuals with borderline von Willebrand factor plasma levelsP Bucciarelli, S M Siboni, F Stufano, et al.
Journal of Thrombosis and Haemostasis : JTH|July 4, 2013
The type 2B p.R1306W natural mutation of von Willebrand factor dramatically enhances the multimer sensitivity to shear stressG L Scaglione, S Lancellotti, M Papi, et al.
Alimentary Pharmacology & Therapeutics|January 31, 2006
Variants of OCTN1-2 cation transporter genes are associated with both Crohn's disease and ulcerative colitisO Palmieri, A Latiano, R Valvano, et al.
Blood|March 26, 1999
Molecular analysis of the ERGIC-53 gene in 35 families with combined factor V-factor VIII deficiencyM Neerman-Arbez, K M Johnson, M A Morris, et al.
Journal of Thrombosis and Haemostasis : JTH|June 16, 2015
Plasma ADAMTS-13 levels and the risk of myocardial infarction: an individual patient data meta-analysisA Maino, B Siegerink, L A Lotta, et al.
Orphanet Journal of Rare Diseases|June 23, 2022
Lombardy diagnostic and therapeutic network of thrombotic microangiopathyI Mancini, P Agosti, M Boscarino, et al.
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