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Journal of Thrombosis and Haemostasis : JTH
|
November 27, 2014
Predictors of von Willebrand disease diagnosis in individuals with borderline von Willebrand factor plasma levels
P 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 stress
G 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 colitis
O 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 deficiency
M Neerman-Arbez, K M Johnson, M A Morris, et al.
Journal of Thrombosis and Haemostasis : JTH
|
December 9, 2017
Pharmacokinetics, clot strength and safety of a new fibrinogen concentrate: randomized comparison with active control in congenital fibrinogen deficiency
C Ross, S Rangarajan, M Karimi, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
June 25, 2008
Genetic aspects and research development in haemostasis
E G Tuddenham, J Ingerslev, L Norengaard Sørensen, 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-analysis
A Maino, B Siegerink, L A Lotta, et al.
Orphanet Journal of Rare Diseases
|
June 23, 2022
Lombardy diagnostic and therapeutic network of thrombotic microangiopathy
I Mancini, P Agosti, M Boscarino, et al.
Blood Advances
|
November 13, 2019
Thrombotic thrombocytopenic purpura and defective apoptosis due to CASP8/10 mutations: the role of mycophenolate mofetil
F Fioredda, E Cappelli, A Mariani, et al.
Scientific Reports
|
November 6, 2022
Reduced circulating FABP2 in patients with moderate to severe COVID-19 may indicate enterocyte functional change rather than cell death
G Assante, A Tourna, R Carpani, et al.
Page
of 17
Search research articles
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Showing results (151-160 of 166) with videos related to
Sort By:
Page
of 17
Journal of Thrombosis and Haemostasis : JTH
|
November 27, 2014
Predictors of von Willebrand disease diagnosis in individuals with borderline von Willebrand factor plasma levels
P 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 stress
G 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 colitis
O 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 deficiency
M Neerman-Arbez, K M Johnson, M A Morris, et al.
Journal of Thrombosis and Haemostasis : JTH
|
December 9, 2017
Pharmacokinetics, clot strength and safety of a new fibrinogen concentrate: randomized comparison with active control in congenital fibrinogen deficiency
C Ross, S Rangarajan, M Karimi, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
June 25, 2008
Genetic aspects and research development in haemostasis
E G Tuddenham, J Ingerslev, L Norengaard Sørensen, 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-analysis
A Maino, B Siegerink, L A Lotta, et al.
Orphanet Journal of Rare Diseases
|
June 23, 2022
Lombardy diagnostic and therapeutic network of thrombotic microangiopathy
I Mancini, P Agosti, M Boscarino, et al.
Blood Advances
|
November 13, 2019
Thrombotic thrombocytopenic purpura and defective apoptosis due to CASP8/10 mutations: the role of mycophenolate mofetil
F Fioredda, E Cappelli, A Mariani, et al.
Scientific Reports
|
November 6, 2022
Reduced circulating FABP2 in patients with moderate to severe COVID-19 may indicate enterocyte functional change rather than cell death
G Assante, A Tourna, R Carpani, et al.
Page
of 17