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- 1999
-
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
- 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
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
Genetic and phenotypic analysis of a large (122-member) protein S-deficient kindred provides an explanation for the familial coexistence of type I and type III plasma phenotypes
Simmonds, Rachel E. ; Zöller, Bengt LU
; Ireland, Helen
; Thompson, Elizabeth
; García De Frutos, Pablo
LU
; Dahlbäck, Björn
LU
and Lane, David A.
(1997)
In Blood
89(12).
p.4364-4370
- Contribution to journal › Article
-
Mark
Evaluation of original and modified APC-resistance tests in unselected outpatients with clinically suspected thrombosis and in healthy controls
Svensson, Peter LU ; Zöller, Bengt LU
and Dahlbäck, Björn
LU
(1997)
In Thrombosis and Haemostasis
77(2).
p.332-335
- Contribution to journal › Article
-
Mark
The factor VR5O6Q mutation causing APC resistance is highly prevalent amongst unselected outpatients with clinically suspected deep venous thrombosis
Svensson, P.J. LU ; Zöller, B. LU
; Mattiasson, I.
LU
and Dahlbäck, B.
LU
(1997)
In Journal of Internal Medicine
241(5).
p.379-385
- Contribution to journal › Article
- 1996
-
Mark
Familial thrombophilia : clinical and molecular analysis of Swedish families with inherited resistance to activated protein C or protein S deficiency
Zöller, Bengt LU
(1996)
In Scandinavian journal of clinical and laboratory investigation. Supplementum
56(226).
p.19-46
- Contribution to journal › Scientific review
-
Mark
Resistance to activated protein C, the FV:Q506 allele, and venous thrombosis
Dahlbäck, Björn LU ; Hillarp, A. LU ; Rosen, S. and Zöller, Bengt LU
(1996)
In Annals of Hematology
72(4).
p.166-176
- Contribution to journal › Scientific review
-
Mark
Inherited resistance to activated protein C caused by presence of the FV:Q506 allele as a basis of venous thrombosis
Dahlbäck, Björn LU ; Zöller, Bengt LU
and Hillarp, Andreas
LU
(1996)
In Haemostasis
26(SUPPL. 4).
p.301-314
- Contribution to journal › Article
- 1995
-
Mark
Activated protein C resistance : from phenotype to genotype and clinical practice
Hillarp, Andreas LU ; Dahlbäck, Björn LU and Zöller, Bengt LU
(1995)
In Blood Reviews
9(4).
p.201-212
- Contribution to journal › Article