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- 2000
-
Mark
Använd hela "analyspaketet" vid utredning av trombospatienten! Och glöm inte släktingarna ...
Persson, Kristina LU
; Hillarp, Andreas
LU
; Lethagen, Stefan
LU
; Berntorp, Erik
LU
and Dahlbäck, Björn
LU
(2000)
In Läkartidningen
97(47).
p.5452-5456
- Contribution to journal › Article
- 1999
-
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
-
Mark
Probing the activation of protein C by the thrombin-thrombomodulin complex using structural analysis, site-directed mutagenesis, and computer modeling
- Contribution to journal › Article
-
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
Activated protein C resistance in patients with peripheral vascular disease
- Contribution to journal › Article
-
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
-
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