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2022
Mark Genetic variation of the blood coagulation regulator tissue factor pathway inhibitor and venous thromboembolism among middle-aged and older adults: A population-based cohort study
Manderstedt, E. ; Elf, J. ^LU ; Svensson, P.J. ^LU ; Engström, G. ^LU ; Melander, O. ^LU and Zöller, B. ^LU (2022) In Research and practice in thrombosis and haemostasis 6(7).
- Contribution to journal › Letter
Mark Classic Thrombophilias and Thrombotic Risk Among Middle-Aged and Older Adults : A Population-Based Cohort Study
Manderstedt, Eric ^LU ; Lind-Halldén, Christina ^LU ; Halldén, Christer ^LU ; Elf, Johan ^LU ; Svensson, Peter J. ^LU ; Dahlbäck, Björn ^LU ; Engström, Gunnar ^LU ; Melander, Olle ^LU ; Baras, Aris and Lotta, Luca A. , et al. (2022) In Journal of the American Heart Association 11(4).
- Contribution to journal › Article
2020
Mark Genetic risk factors for venous thromboembolism
Zöller, Bengt ^LU ; Svensson, Peter J. ^LU ; Dahlbäck, Björn ^LU ; Lind-Hallden, Christina ^LU ; Hallden, Christer ^LU and Elf, Johan ^LU (2020) In Expert Review of Hematology 13(9). p.971-981
- Contribution to journal › Scientific review
2016
Mark Epidemiology of Familial Aggregation of Venous Thromboembolism
Zöller, Bengt ^LU ; Li, Xinjun ^LU ; Ohlsson, Henrik ^LU ; Ji, Jianguang ^LU ; Memon, Ashfaque A. ^LU ; Svensson, Peter J. ^LU ; Palmér, Karolina ^LU ; Dahlbäck, Björn ^LU ; Sundquist, Jan ^LU and Sundquist, Kristina ^LU (2016) In Seminars in Thrombosis and Hemostasis 42(8). p.821-832
- Contribution to journal › Scientific review
2012
Mark Small and large PROS1 deletions but no other types of rearrangements detected in patents with protein S deficiency
Lind-Hallden, Christina ; Dahlen, Anna ; Hillarp, Andreas ^LU ; Zöller, Bengt ^LU ; Dahlbäck, Björn ^LU and Hallden, Christer (2012) In Thrombosis and Haemostasis 108(1). p.94-100
- Contribution to journal › Article
2002
Mark Genetic and phenotypic variability between families with hereditary protein S deficiency
Rezende, SM ; Lane, DA ; Zöller, Bengt ^LU ; Mille-Baker, B ; Laffan, M ; Dahlbäck, Björn ^LU and Simmonds, RE (2002) In Thrombosis and Haemostasis 87(2). p.258-265
- Contribution to journal › Article
1999
Mark Thrombophilia as a multigenic disease
Zöller, Bengt ^LU ; Garcia de Frutos, Pablo ^LU ; Hillarp, A ^LU and Dahlbäck, Björn ^LU (1999) In Haematologica 84(1). p.59-70
- Contribution to journal › Article
1998
Mark The A20210 allele of the prothrombin gene is frequently associated with the factor V Arg 506 to Gln mutation but not with protein S deficiency in thrombophilic families
Zöller, Bengt ^LU ; Svensson, P J ^LU ; Dahlbäck, Björn ^LU and Hillarp, A ^LU (1998) In Blood 91(6). p.1-2210
- Contribution to journal › Letter
Mark The A20210 allele of the prothrombin gene is frequently associated with the factor V Arg 506 to Gln mutation but not with protein S deficiency in thrombophilic families [3]
Zöller, Bengt ^LU ; Svensson, P.J. ^LU ; Dahlbäck, Björn ^LU and Hillarp, A. ^LU (1998) In Blood 91(6). p.2210-2211
- Contribution to journal › Letter
1997
Mark A novel thrombomodulin gene mutation in a patient suffering from sagittal sinus thrombosis
Norlund, Lena ^LU ; Zöller, Bengt ^LU and Öhlin, Ann-Kristin ^LU (1997) In Thrombosis and Haemostasis 78(4). p.1164-1166
- Contribution to journal › Article

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