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The British Journal of Surgery
|
June 12, 2013
Raised haematocrit concentration and the risk of death and vascular complications after major surgery
K 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 Iran
M 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.
Journal of Thrombosis and Haemostasis : JTH
|
April 27, 2017
Caplacizumab reduces the frequency of major thromboembolic events, exacerbations and death in patients with acquired thrombotic thrombocytopenic purpura
F Peyvandi, M Scully, J A Kremer Hovinga, et al.
Journal of Thrombosis and Haemostasis : JTH
|
July 6, 2011
Platelet reactive conformation and multimeric pattern of von Willebrand factor in acquired thrombotic thrombocytopenic purpura during acute disease and remission
L A Lotta, R Lombardi, M Mariani, et al.
Journal of Thrombosis and Haemostasis : JTH
|
October 13, 2018
Hemostatic abnormalities in patients with Ehlers-Danlos syndrome
A Artoni, A Bassotti, M Abbattista, et al.
Journal of Thrombosis and Haemostasis : JTH
|
May 25, 2011
Oxidized von Willebrand factor is efficiently cleaved by serine proteases from primary granules of leukocytes: divergence from ADAMTS-13
S Lancellotti, V De Filippis, N Pozzi, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
May 5, 2011
Central nervous system bleeding in patients with rare bleeding disorders
S M Siboni, E Zanon, G Sottilotta, et al.
Journal of Thrombosis and Haemostasis : JTH
|
November 29, 2015
Thrombotic microangiopathy without renal involvement: two novel mutations in complement-regulator genes
F Peyvandi, R Rossio, B Ferrari, et al.
Journal of Thrombosis and Haemostasis : JTH
|
February 28, 2009
Major differences in bleeding symptoms between factor VII deficiency and hemophilia B
F Bernardi, A Dolce, M Pinotti, et al.
Page
of 17
Search research articles
Search
Showing results (131-140 of 166) with videos related to
Sort By:
Page
of 17
The British Journal of Surgery
|
June 12, 2013
Raised haematocrit concentration and the risk of death and vascular complications after major surgery
K 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 Iran
M 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.
Journal of Thrombosis and Haemostasis : JTH
|
April 27, 2017
Caplacizumab reduces the frequency of major thromboembolic events, exacerbations and death in patients with acquired thrombotic thrombocytopenic purpura
F Peyvandi, M Scully, J A Kremer Hovinga, et al.
Journal of Thrombosis and Haemostasis : JTH
|
July 6, 2011
Platelet reactive conformation and multimeric pattern of von Willebrand factor in acquired thrombotic thrombocytopenic purpura during acute disease and remission
L A Lotta, R Lombardi, M Mariani, et al.
Journal of Thrombosis and Haemostasis : JTH
|
October 13, 2018
Hemostatic abnormalities in patients with Ehlers-Danlos syndrome
A Artoni, A Bassotti, M Abbattista, et al.
Journal of Thrombosis and Haemostasis : JTH
|
May 25, 2011
Oxidized von Willebrand factor is efficiently cleaved by serine proteases from primary granules of leukocytes: divergence from ADAMTS-13
S Lancellotti, V De Filippis, N Pozzi, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
May 5, 2011
Central nervous system bleeding in patients with rare bleeding disorders
S M Siboni, E Zanon, G Sottilotta, et al.
Journal of Thrombosis and Haemostasis : JTH
|
November 29, 2015
Thrombotic microangiopathy without renal involvement: two novel mutations in complement-regulator genes
F Peyvandi, R Rossio, B Ferrari, et al.
Journal of Thrombosis and Haemostasis : JTH
|
February 28, 2009
Major differences in bleeding symptoms between factor VII deficiency and hemophilia B
F Bernardi, A Dolce, M Pinotti, et al.
Page
of 17