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- 1999
-
Mark
The prothrombin gene G20210A mutation and the platelet glycoprotein IIIa polymorphism PlA2 in patients with central retinal vein occlusion
- Contribution to journal › Article
- 1998
-
Mark
The Fy(x) phenotype is associated with a missense mutation in the Fy(b) allele predicting Arg89Cys in the Duffy glycoprotein
Olsson, Martin L LU
; Smythe, J S
; Hansson, Carola
; Poole, J
; Mallinson, G
; Jones, J
; Avent, N D
and Daniels, G
(1998)
In British Journal of Haematology
103(4).
p.1184-1191
- Contribution to journal › Article
-
Mark
Inverse relationship between GAD65 antibody levels and severe retinopathy in younger type 1 diabetic patients
Agardh, Daniel LU ; Agardh, Elisabet LU ; Landin-Olsson, Mona LU ; Gaur, Lakshmi K ; Agardh, Carl-David LU and Lernmark, Åke LU
(1998)
In Diabetes Research and Clinical Practice
40(1).
p.9-14
- 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
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
Relation of alleles of the collagen type Ialpha1 gene to bone density and the risk of osteoporotic fractures in postmenopausal women
Uitterlinden, A G ; Burger, H ; Huang, Q ; Yue, F ; McGuigan, F E LU
; Grant, S F
; Hofman, A
; van Leeuwen, J P
; Pols, H A
and Ralston, S H
(1998)
In New England Journal of Medicine
338(15).
p.21-1016
- Contribution to journal › Article
- 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
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
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
Polymorphisms of the interleukin-6 gene are associated with bone mineral density
Murray, R E ; McGuigan, F LU
; Grant, S F
; Reid, D M
and Ralston, S H
(1997)
In Bone
21(1).
p.89-92
- Contribution to journal › Article