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2023
Mark "Hereditary angioedema is associated with an increased risk of venous thromboembolism" : reply
Grover, Steven P. ; Björkman, Linda Sundler ^LU ; Egesten, Arne ^LU ; Moll, Stephan and Mackman, Nigel (2023) In Journal of thrombosis and haemostasis : JTH 21(1). p.180-182
- Contribution to journal › Letter
2022
Mark Diagnosis and management of severe congenital protein C deficiency (SCPCD) : Communication from the SSC of the ISTH
Minford, Adrian ; Brandão, Leonardo R. ; Othman, Maha ; Male, Christoph ; Abdul-Kadir, Rezan ; Monagle, Paul ; Mumford, Andrew D. ; Adcock, Dorothy ; Dahlbäck, Björn ^LU and Miljic, Predrag , et al. (2022) In Journal of Thrombosis and Haemostasis 20(7). p.1735-1743
- Contribution to journal › Article
Mark Von Willebrand factor propeptide and pathophysiological mechanisms in European and Iranian patients with type 3 von Willebrand disease enrolled in the 3WINTERS-IPS study
Pagliari, Maria Teresa ; Rosendaal, Frits R. ; Ahmadinejad, Minoo ; Badiee, Zahra ; Baghaipour, Mohammad Reza ; Baronciani, Luciano ; Benítez Hidalgo, Olga ; Bodó, Imre ; Budde, Ulrich and Castaman, Giancarlo , et al. (2022) In Journal of Thrombosis and Haemostasis 20(5). p.1106-1114
- Contribution to journal › Article
Mark The preAR2 region (1458–1492) in factor V-Short is crucial for the synergistic TFPIα-cofactor activity with protein S and the assembly of a trimolecular factor Xa-inhibitory complex comprising FV-Short, protein S, and TFPIα
Dahlbäck, Björn ^LU and Tran, Sinh ^LU (2022) In Journal of Thrombosis and Haemostasis 20(1). p.58-68
- Contribution to journal › Article
Mark A hydrophobic patch (PLVIVG; 1481–1486) in the B-domain of factor V-short is crucial for its synergistic TFPIα-cofactor activity with protein S and for the formation of the FXa-inhibitory complex comprising FV-short, TFPIα, and protein S
Dahlbäck, Björn ^LU and Tran, Sinh ^LU (2022) In Journal of Thrombosis and Haemostasis 20(5). p.1146-1157
- Contribution to journal › Article
Mark Thrombotic risk determined by rare and common SERPINA1 variants in a population-based cohort study
Manderstedt, E. ; Halldén, Christer ; Lind-Halldén, Christina ; Elf, J. ^LU ; Svensson, P.J. ^LU ; Engström, G. ^LU ; Melander, O. ^LU ; Baras, Aris ; Lotta, Luca A. and Zöller, B. ^LU (2022) In Journal of Thrombosis and Haemostasis 20(6).
- Contribution to journal › Article
Mark Thrombomodulin (THBD) gene variants and thrombotic risk in a population-based cohort study
Manderstedt, Eric ; Halldén, Christer ; Lind-Halldén, Christina ; Elf, Johan ^LU ; Svensson, Peter J. ^LU ; Engström, Gunnar ^LU ; Melander, Olle ^LU ; Baras, Aris ; Lotta, Luca A. and Zöller, Bengt ^LU (2022) In Journal of Thrombosis and Haemostasis 20(4). p.929-935
- Contribution to journal › Article
Mark Hereditary angioedema is associated with an increased risk of venous thromboembolism
Grover, Steven P. ; Sundler Björkman, Linda ^LU ; Egesten, Arne ^LU ; Moll, Stephan and Mackman, Nigel (2022) In Journal of Thrombosis and Haemostasis 20(11). p.2703-2706
- Contribution to journal › Letter
2021
Mark Suggested treatment of serious complications to COVID-19 vaccination with IdeS, a bacterial antibody-cleaving enzyme
Kahn, Fredrik ^LU ; Shannon, Oonagh ^LU and Björck, Lars ^LU (2021) In Journal of Thrombosis and Haemostasis 19(9). p.2363-2364
- Contribution to journal › Letter
Mark The Copenhagen founder variant GP1BA c.58T>G is the most frequent cause of inherited thrombocytopenia in Denmark
Leinøe, Eva ; Brøns, Nanna ; Rasmussen, Andreas Ørslev ; Gabrielaite, Migle ; Zaninetti, Carlo ; Palankar, Raghavendra ; Zetterberg, Eva ^LU ; Rosthøj, Steen ; Ostrowski, Sisse Rye and Rossing, Maria (2021) In Journal of Thrombosis and Haemostasis 19(11). p.2884-2892
- Contribution to journal › Article

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