81 – 90 of 97
- show: 10
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=""
width=""
height=""
allowtransparency="true"
frameborder="0">
</iframe>
- 2001
-
Mark
Somatic mosaicism in hemophilia A: A fairly common event
Leuer, M. ; Lavergne, J.-M. ; Fregin, A. ; Eigel, A. ; Ljung, R. LU
and Olek, K.
(2001)
In American Journal of Human Genetics
69(1).
p.75-87
- Contribution to journal › Article
- 2000
-
Mark
Treatment of children with haemophilia in Europe: A survey of 20 centres in 16 countries
Ljung, R. LU
; Aronis-Vournas, S.
; Kurnik-Auberger, K.
; van den Berg, M
; Chambost, H
; Claeyssens, S
; Van Geet, C.
; Glomstein, A
; Hann, I.
and Hill, F
, et al.
(2000)
In Haemophilia
6.
p.619-624
- Contribution to journal › Article
- 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
-
Mark
Prevalence of IgA-antiendomysium and IgA-antigliadin autoantibodies at diagnosis of insulin-dependent diabetes mellitus in Swedish children and adolescents
Carlsson, Annelie LU
; Axelsson, Irene E. M.
LU
; Borulf, Stefan K.
LU
; Bredberg, Anders C. A.
LU
; Lindberg, Bengt A.
LU
; Sjöberg, Klas G.
LU
and Ivarsson, Sten-A.
LU
(1999)
In Pediatrics
103(6 I).
p.1248-1252
- Contribution to journal › Article
-
Mark
Prevalence of coeliac disease in Turner syndrome
Ivarsson, S-A ; Carlsson, A. LU
; Bredberg, A.
LU
; Alm, J.
; Aronsson, S
; Gustafsson, J.
; Hagenäs, Lars
; Häger, A.
; Kriström, Berit
and Marcus, C
, et al.
(1999)
In Acta Pædiatrica
88(9).
p.933-936
- Contribution to journal › Article
-
Mark
Long-term psychological effects of carrier testing and prenatal diagnosis of haemophilia: Comparison with a control group
- Contribution to journal › Article
- 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
-
Mark
Can haemophilic arthropathy be prevented?
- Contribution to journal › Special issue (editor)
-
Mark
Social desirability and self-reported anxiety in children: An analysis of the RCMAS lie scale
Dadds, Mark R. ; Perrin, Sean LU
and Yule, William
(1998)
In Journal of Abnormal Child Psychology
26(4).
p.311-317
- Contribution to journal › Article