-
1
-
-
84893966985
-
World federation of Haemophilia
-
27/01/2011
-
Report on the Global Survey 2008. World federation of Haemophilia. Available at: www1.wfh.org/publications/files/ pdf-1429.pdf. Accessed on: 27/01/2011.
-
(2008)
Report on the Global Survey
-
-
-
2
-
-
0013836217
-
Haemophilia in Sweden
-
VII. Incidence, treatment and prophylaxis of arthropathy and other musculo-skeletal manifestations of haemophilia A and B.
-
Ahlberg A. Haemophilia in Sweden. VII. Incidence, treatment and prophylaxis of arthropathy and other musculo-skeletal manifestations of haemophilia A and B. Acta Orthop Scand 1965; Suppl. 77: 3-132.
-
(1965)
Acta Orthop Scand
, vol.77 SUPPL.
, pp. 3-132
-
-
Ahlberg, A.1
-
3
-
-
9444232777
-
Thirty years of hemophilia treatment in the Netherlands, 1972-2001
-
Plug I, van der Bom JG, Peters M, et al. Thirty years of hemophilia treatment in the Netherlands, 1972-2001. Blood 2004; 104: 3494-500.
-
(2004)
Blood
, vol.104
, pp. 3494-3500
-
-
Plug, I.1
Van Der Bom, J.G.2
Peters, M.3
-
4
-
-
63049103181
-
Clinical outcome of moderate haemophilia compared with severe and mild haemophilia
-
den Uijl IEM, Fischer K, van der Bom JG, et al. Clinical outcome of moderate haemophilia compared with severe and mild haemophilia. Haemophilia 2009; 15: 83-90.
-
(2009)
Haemophilia
, vol.15
, pp. 83-90
-
-
Den Uijl, I.E.M.1
Fischer, K.2
Van Der Bom, J.G.3
-
5
-
-
33646003882
-
Compliance with treatment and understanding of own disease in patients with severe and moderate haemophilia
-
Lindvall K, Colstrup L, Wollter IM, et al. Compliance with treatment and understanding of own disease in patients with severe and moderate haemophilia. Haemophilia 2006; 12: 47-51.
-
(2006)
Haemophilia
, vol.12
, pp. 47-51
-
-
Lindvall, K.1
Colstrup, L.2
Wollter, I.M.3
-
6
-
-
33747169861
-
Hemophilia joint health score reliability study
-
Hilliard P, Funk S, Zourikian N, et al. Hemophilia joint health score reliability study. Haemophilia 2006; 12: 518-25.
-
(2006)
Haemophilia
, vol.12
, pp. 518-525
-
-
Hilliard, P.1
Funk, S.2
Zourikian, N.3
-
7
-
-
0000592120
-
Psychometric qualities of the RAND 36-Item Health Survey 1.0: A multidimensional measure of general health status
-
VanderZee KI, Sanderman R, Heyink JW, de Haes H. Psychometric qualities of the RAND 36-Item Health Survey 1.0: a multidimensional measure of general health status. Int J Behav Med 1996; 3: 104-22.
-
(1996)
Int J Behav Med
, vol.3
, pp. 104-122
-
-
Vanderzee, K.I.1
Sanderman, R.2
Heyink, J.W.3
De Haes, H.4
-
8
-
-
0037950631
-
Validity and feasibility of the use of condition-specific outcome measures in economic evaluation
-
Stolk EA, Busschbach JJ. Validity and feasibility of the use of condition-specific outcome measures in economic evaluation. Qual Life Res 2003; 12: 363-71.
-
(2003)
Qual Life Res
, vol.12
, pp. 363-371
-
-
Stolk, E.A.1
Busschbach, J.J.2
-
9
-
-
33645997025
-
Measuring patients' perceptions on their functional abilities: Validation of the Haemophilia Activities List
-
van Genderen FR, Westers P, Heijnen L, et al. Measuring patients' perceptions on their functional abilities: validation of the Haemophilia Activities List. Haemophilia 2006; 12: 36-46.
-
(2006)
Haemophilia
, vol.12
, pp. 36-46
-
-
Van Genderen, F.R.1
Westers, P.2
Heijnen, L.3
-
10
-
-
0021752980
-
Methodology of the one-stage assay of factor VIII (VIII:C)
-
Over J. Methodology of the one-stage assay of factor VIII (VIII:C). Scand J Haematol Suppl 1984; 41: 13-24.
-
(1984)
Scand J Haematol Suppl
, vol.41
, pp. 13-24
-
-
Over, J.1
-
11
-
-
0021153954
-
Changes in coagulation parameters with exercise in patients with classic hemophilia
-
Koch B, Luban NL, Galioto FM, et al. Changes in coagulation parameters with exercise in patients with classic hemophilia. Am J Hematol 1984; 16: 227-33.
-
(1984)
Am J Hematol
, vol.16
, pp. 227-233
-
-
Koch, B.1
Luban, N.L.2
Galioto, F.M.3
-
12
-
-
4644353081
-
SSC/ISTH classification of hemophilia A: Can hemophilia center laboratories achieve the new criteria?
-
Preston FE, Kitchen S, Jennings I, et al. SSC/ISTH classification of hemophilia A: can hemophilia center laboratories achieve the new criteria? J Thromb Haemost 2004; 2: 271-4.
-
(2004)
J Thromb Haemost
, vol.2
, pp. 271-274
-
-
Preston, F.E.1
Kitchen, S.2
Jennings, I.3
-
13
-
-
54149087646
-
Less severe bleeding in hemophilia B than in hemophilia A
-
Lowe GD, Ludlam CA. Less severe bleeding in hemophilia B than in hemophilia A. J. Thromb Haemost 2008; 6: 1982-3.
-
(2008)
J Thromb Haemost
, vol.6
, pp. 1982-1983
-
-
Lowe, G.D.1
Ludlam, C.A.2
-
14
-
-
0034537746
-
Endogenous clotting factor activity and long-term outcome in patients with moderate haemophilia
-
Fischer K, van der Bom JG, Mauser-Bunschoten EP, et al. Endogenous clotting factor activity and long-term outcome in patients with moderate haemophilia. Thromb Haemost 2000; 84: 977-80.
-
(2000)
Thromb Haemost
, vol.84
, pp. 977-980
-
-
Fischer, K.1
Van Der Bom, J.G.2
Mauser-Bunschoten, E.P.3
-
15
-
-
0036529818
-
The effects of postponing prophylactic treatment on long-term outcome in patients with severe hemophilia
-
Fischer K, van der Bom JG, Mauser-Bunschoten EP, et al. The effects of postponing prophylactic treatment on long-term outcome in patients with severe hemophilia. Blood 2002; 99: 2337-41.
-
(2002)
Blood
, vol.99
, pp. 2337-2341
-
-
Fischer, K.1
Van Der Bom, J.G.2
Mauser-Bunschoten, E.P.3
-
16
-
-
0033028402
-
Primary prophylaxis in severe haemophilia should be started at an early age but can be individualized
-
Astermark J, Petrini P, Tengborn L, et al. Primary prophylaxis in severe haemophilia should be started at an early age but can be individualized. Br J Haematol 1999; 105: 1109-13.
-
(1999)
Br J Haematol
, vol.105
, pp. 1109-1113
-
-
Astermark, J.1
Petrini, P.2
Tengborn, L.3
|