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- 2014
-
Mark
Determination of 14 Circulating microRNAs in Swedes and Iraqis with and without Diabetes Mellitus Type 2.
Wang, Xiao LU ; Sundquist, Jan LU ; Zöller, Bengt LU
; Memon, Ashfaque
LU
; Palmér, Karolina
LU
; Sundquist, Kristina
LU
and Bennet, Louise
LU
(2014)
In PLoS ONE
9(1).
- 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
- 1998
-
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
- 1997
-
Mark
The 20210 A allele of the prothrombin gene is a common risk factor among Swedish outpatients with verified deep venous thrombosis
Hillarp, Andreas LU ; Zöller, Bengt LU
; Svensson, Peter
LU
and Dahlbäck, Björn
LU
(1997)
In Thrombosis and Haemostasis
78(3).
p.2-990
- Contribution to journal › Debate/Note/Editorial
-
Mark
Activated protein C resistance caused by a common factor V mutation has a single origin
Zöller, Bengt LU
; Hillarp, Andreas
LU
and Dahlbäck, Björn
LU
(1997)
In Thrombosis Research
85(3).
p.43-237
- Contribution to journal › Article
-
Mark
The factor VR506Q mutation causing APC resistance is highly prevalent amongst unselected outpatients with clinically suspected deep venous thrombosis
Svensson, Peter LU ; Zöller, Bengt LU
; Mattiasson, Ingrid
LU
and Dahlbäck, Björn
LU
(1997)
In Journal of Internal Medicine
241(5).
p.379-385
- Contribution to journal › Article
-
Mark
A common thrombomodulin amino acid dimorphism is associated with myocardial infarction
Norlund, Lena LU ; Holm, Johan LU ; Zöller, Bengt LU
and Öhlin, Ann-Kristin
LU
(1997)
In Thrombosis and Haemostasis
77(2).
p.51-248
- Contribution to journal › Article
- 1996
-
Mark
Elevated levels of prothrombin activation fragment 1 + 2 in plasma from patients with heterozygous Arg506 to Gln mutation in the factor V gene (APC-resistance) and/or inherited protein S deficiency
Zöller, Bengt LU
; Holm, Johan
LU
; Svensson, Peter
LU
and Dahlbäck, B
LU
(1996)
In Thrombosis and Haemostasis
75(2).
p.270-274
- Contribution to journal › Article
-
Mark
Prevalence of factor V gene mutation amongst myocardial infarction patients and healthy controls is higher in Sweden than in other countries
Holm, Johan LU ; Zöller, Bengt LU
; Berntorp, Erik
LU
; Erhardt, Leif RW
LU
and Dahlbäck, Björn
LU
(1996)
In Journal of Internal Medicine
239(3).
p.221-226
- Contribution to journal › Article
-
Mark
High prevalence of the FVR506Q mutation causing APC resistance in a region of southern Sweden with a high incidence of venous thrombosis.
Zöller, Bengt LU
; Norlund, L
LU
; Leksell, Håkan
; Nilsson, Jan-Erik
; von Schenck, Henning
; Rosén, Ulf
; Jepsson, J O
and Dahlbäck, Björn
LU
(1996)
In Thrombosis Research
83(6).
p.475-477
- Contribution to journal › Letter