Bengt Zöller
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- 2002
-
Mark
Naturally occurring mutations in the thrombomodulin gene leading to impaired expression and function
Kunz, G ; Öhlin, Ann-Kristin LU ; Adami, A ; Zöller, Bengt LU
; Svensson, P
and Lane, DA
(2002)
In Blood
99(10).
p.3646-3653
- Contribution to journal › Article
-
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
- 2001
-
Mark
Improved hemoglobin status and reduced menstrual blood loss among female carriers of factor V Leiden--an evolutionary advantage?
Lindqvist, Pelle LU ; Zöller, Bengt LU
and Dahlbäck, Björn
LU
(2001)
In Thrombosis and Haemostasis
86(4).
p.1122-1123
- Contribution to journal › Letter
- 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
-
Mark
The Ala25-Thr mutation in the thrombomodulin gene is not frequent in Swedish patients suffering from ischemic heart disease [9]
Norlund, Lena LU ; Holm, J. LU ; Zöller, Bengt LU
and Öhlin, Ann-Kristin
LU
(1999)
In Thrombosis and Haemostasis
82(4).
p.1367-1368
- Contribution to journal › Letter
-
Mark
Factor V Q506 (resistance to activated protein C) and prognosis after acute coronary syndrome
Holm, Johan LU ; Hillarp, Andreas LU ; Zöller, Bengt LU
; Erhardt, Leif RW
LU
; Berntorp, Erik
LU
and Dahlbäck, Björn
LU
(1999)
In Thrombosis and Haemostasis
81(6).
p.857-860
- Contribution to journal › Article
- 1998
-
Mark
A common 4G allele in the promoter of the plasminogen activator inhibitor-1 (PAI-1) gene as a risk factor for pulmonary embolism and arterial thrombosis in hereditary protein S deficiency
Zöller, Bengt LU
; Garcia de Frutos, Pablo
LU
and Dahlbäck, B
LU
(1998)
In Thrombosis and Haemostasis
79(4).
p.802-807
- Contribution to journal › Article
-
Mark
A new direct, fast and quantitative enzyme-linked ligandsorbent assay for measurement of free protein S antigen
Giri, Tusar K LU ; Hillarp, Andreas LU ; Härdig, Ylva ; Zöller, Bengt LU
and Dahlbäck, Björn
LU
(1998)
In Thrombosis and Haemostasis
79(4).
p.767-772
- Contribution to journal › Article
-
Mark
Clarification of the risk for venous thrombosis associated with hereditary protein S deficiency by investigation of a large kindred with a characterized gene defect
Simmonds, R E ; Ireland, H ; Lane, D A ; Zöller, B LU
; García de Frutos, P
and Dahlbäck, B
LU
(1998)
In Annals of Internal Medicine
128(1).
p.8-14
- Contribution to journal › Article
-
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