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- 1999
-
Mark
Prenatal diagnosis of haemophilia
- Contribution to journal › Scientific review
-
Mark
HLA associations in type 1 diabetes among patients not carrying high-risk DR3-DQ2 or DR4-DQ8 haplotypes
Undlien, Dag E. ; Kockum, I. ; Rønningen, K. S. ; Lowe, R. ; Saanjeevi, C. B. ; Graham, J. ; Lie, B. A. ; Akselsen, H. E. ; Lernmark, Å LU
and Thorsby, E.
(1999)
In Tissue Antigens
54(6).
p.543-551
- Contribution to journal › Article
-
Mark
The prothrombin gene G20210A mutation and the platelet glycoprotein IIIa polymorphism PlA2 in patients with central retinal vein occlusion
- Contribution to journal › Article
-
Mark
The vitamin D receptor (VDR) start codon polymorphism in primary hyperparathyroidism and parathyroid VDR messenger ribonucleic acid levels
- 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
Phenotypes and genotypes in families with hereditary tapetoretinal degenerations
(1997)
- Thesis › Doctoral thesis (compilation)