-
1
-
-
47649096167
-
Guideline on the selection and use of therapeutic products to treat haemophilia and other hereditary bleeding disorders
-
Keeling D, Tait C, Makris M. Guideline on the selection and use of therapeutic products to treat haemophilia and other hereditary bleeding disorders. Haemophilia 2008; 14: 671-84.
-
(2008)
Haemophilia
, vol.14
, pp. 671-684
-
-
Keeling, D.1
Tait, C.2
Makris, M.3
-
2
-
-
33750988816
-
Inhibitor treatment in haemophilias A and B: Summary statement for the 2006 international consensus conference
-
Berntorp E, Shapiro A, Astermark J et al. Inhibitor treatment in haemophilias A and B: Summary statement for the 2006 international consensus conference. Haemophilia 2006; 12 (Suppl 6): 1-7.
-
(2006)
Haemophilia
, vol.12
, Issue.SUPPL. 6
, pp. 1-7
-
-
Berntorp, E.1
Shapiro, A.2
Astermark, J.3
-
3
-
-
24944440876
-
Environmental risk factors for inhibitor development in children with haemophilia A: A case-control study
-
Santagostino E, Mancuso ME, Rocino A et al. Environmental risk factors for inhibitor development in children with haemophilia A: A case-control study. Br J Haematol 2005; 130: 422-7.
-
(2005)
Br J Haematol
, vol.130
, pp. 422-427
-
-
Santagostino, E.1
Mancuso, M.E.2
Rocino, A.3
-
4
-
-
33846922841
-
Early factor VIII exposure and subsequent inhibitor development in children with severe haemophilia A
-
Chalmers EA, Brown SA, Keeling D et al. Early factor VIII exposure and subsequent inhibitor development in children with severe haemophilia A. Haemophilia 2007; 13: 149-55.
-
(2007)
Haemophilia
, vol.13
, pp. 149-155
-
-
Chalmers, E.A.1
Brown, S.A.2
Keeling, D.3
-
5
-
-
34249690732
-
Treatment-related risk factors of inhibitor development in previously untreated patients with hemophilia A: The CANAL cohort study
-
Gouw SC, van der Bom JG, Marijke van den Berg H. Treatment-related risk factors of inhibitor development in previously untreated patients with hemophilia A: The CANAL cohort study. Blood 2007; 109: 4648-54.
-
(2007)
Blood
, vol.109
, pp. 4648-4654
-
-
Gouw, S.C.1
van der Bom, J.G.2
Marijke van den Berg, H.3
-
6
-
-
0036588771
-
Inhibitors: Resolving diagnostic and therapeutic dilemmas
-
Dimichele D. Inhibitors: Resolving diagnostic and therapeutic dilemmas. Haemophilia 2002; 8: 280-7.
-
(2002)
Haemophilia
, vol.8
, pp. 280-287
-
-
Dimichele, D.1
-
7
-
-
0038383605
-
The epidemiology of inhibitors in haemophilia A: A systematic review
-
Wight J, Paisley S. The epidemiology of inhibitors in haemophilia A: A systematic review. Haemophilia 2003; 9: 418-35.
-
(2003)
Haemophilia
, vol.9
, pp. 418-435
-
-
Wight, J.1
Paisley, S.2
-
8
-
-
12144290833
-
Joint range-of-motion limitations among young males with hemophilia: Prevalence and risk factors
-
Soucie JM, Cianfrini C, Janco RL et al. Joint range-of-motion limitations among young males with hemophilia: Prevalence and risk factors. Blood 2004; 103: 2467-73.
-
(2004)
Blood
, vol.103
, pp. 2467-2473
-
-
Soucie, J.M.1
Cianfrini, C.2
Janco, R.L.3
-
9
-
-
34548304886
-
European Study on Orthopaedic Status of haemophilia patients with inhibitors
-
Morfini M, Haya S, Tagariello G et al. European Study on Orthopaedic Status of haemophilia patients with inhibitors. Haemophilia 2007; 13: 606-12.
-
(2007)
Haemophilia
, vol.13
, pp. 606-612
-
-
Morfini, M.1
Haya, S.2
Tagariello, G.3
-
10
-
-
34248594449
-
A systematic approach to controlling problem bleeds in patients with severe congenital haemophilia A and high-titre inhibitors
-
Teitel J, Berntorp E, Collins P et al. A systematic approach to controlling problem bleeds in patients with severe congenital haemophilia A and high-titre inhibitors. Haemophilia 2007; 13: 256-63.
-
(2007)
Haemophilia
, vol.13
, pp. 256-263
-
-
Teitel, J.1
Berntorp, E.2
Collins, P.3
-
11
-
-
34347360724
-
International workshop on immune tolerance induction: Consensus recommendations
-
DiMichele DM, Hoots WK, Pipe SW, Rivard GE, Santagostino E. International workshop on immune tolerance induction: Consensus recommendations. Haemophilia 2007; 13(Suppl 1): 1-22.
-
(2007)
Haemophilia
, vol.13
, Issue.SUPPL. 1
, pp. 1-22
-
-
DiMichele, D.M.1
Hoots, W.K.2
Pipe, S.W.3
Rivard, G.E.4
Santagostino, E.5
-
12
-
-
40349096477
-
Low-dose immune tolerance induction for paediatric haemophilia patients with factor VIII inhibitors
-
Unuvar A, Kavakli K, Baytan B et al. Low-dose immune tolerance induction for paediatric haemophilia patients with factor VIII inhibitors. Haemophilia 2008; 14: 315-22.
-
(2008)
Haemophilia
, vol.14
, pp. 315-322
-
-
Unuvar, A.1
Kavakli, K.2
Baytan, B.3
-
13
-
-
33845763866
-
Current use of by-passing agents in Europe in the management of acute bleeds in patients with haemophilia and inhibitors
-
Astermark J, Rocino A, Von Depka M et al. Current use of by-passing agents in Europe in the management of acute bleeds in patients with haemophilia and inhibitors. Haemophilia 2007; 13: 38-45.
-
(2007)
Haemophilia
, vol.13
, pp. 38-45
-
-
Astermark, J.1
Rocino, A.2
Von Depka, M.3
-
14
-
-
51249100418
-
Prophylaxis with recombinant factor VIIa for the management of bleeding episodes during immune tolerance treatment in a boy with severe haemophilia A and high-response inhibitors
-
Blatny J, Kohlerova S, Zapletal O, Fiamoli V, Penka M, Smith O. Prophylaxis with recombinant factor VIIa for the management of bleeding episodes during immune tolerance treatment in a boy with severe haemophilia A and high-response inhibitors. Haemophilia 2008; 14: 1140-2.
-
(2008)
Haemophilia
, vol.14
, pp. 1140-1142
-
-
Blatny, J.1
Kohlerova, S.2
Zapletal, O.3
Fiamoli, V.4
Penka, M.5
Smith, O.6
-
15
-
-
33645978414
-
Canadian multi-institutional survey of immune tolerance therapy (ITT) - Experience with the use of recombinant factor VIII for ITT
-
Barnes C, Rivard GE, Poon MC et al. Canadian multi-institutional survey of immune tolerance therapy (ITT) - experience with the use of recombinant factor VIII for ITT. Haemophilia 2006; 12: 1-6.
-
(2006)
Haemophilia
, vol.12
, pp. 1-6
-
-
Barnes, C.1
Rivard, G.E.2
Poon, M.C.3
-
16
-
-
33646686129
-
The diagnosis and management of factor VIII and IX inhibitors: A guideline from the United Kingdom Haemophilia Centre Doctors Organisation
-
Hay CR, Brown S, Collins PW, Keeling DM, Liesner R. The diagnosis and management of factor VIII and IX inhibitors: A guideline from the United Kingdom Haemophilia Centre Doctors Organisation. Br J Haematol 2006; 133: 591-605.
-
(2006)
Br J Haematol
, vol.133
, pp. 591-605
-
-
Hay, C.R.1
Brown, S.2
Collins, P.W.3
Keeling, D.M.4
Liesner, R.5
-
18
-
-
34548308950
-
Meeting report: Ninth and tenth workshops of the European Paediatric Network for Haemophilia Management (PedNet)
-
Kurnik K, Thomas AE. Meeting report: Ninth and tenth workshops of the European Paediatric Network for Haemophilia Management (PedNet). Haemophilia 2007; 13: 658-62.
-
(2007)
Haemophilia
, vol.13
, pp. 658-662
-
-
Kurnik, K.1
Thomas, A.E.2
-
19
-
-
0038383602
-
Control of bleeding in patients with haemophilia A with inhibitors: A systematic review
-
Lloyd Jones M, Wight J, Paisley S, Knight C. Control of bleeding in patients with haemophilia A with inhibitors: A systematic review. Haemophilia 2003; 9: 464-520.
-
(2003)
Haemophilia
, vol.9
, pp. 464-520
-
-
Lloyd Jones, M.1
Wight, J.2
Paisley, S.3
Knight, C.4
-
20
-
-
34548096392
-
Randomized, prospective clinical trial of recombinant factor VIIa for secondary prophylaxis in hemophilia patients with inhibitors
-
Konkle BA, Ebbesen LS, Erhardtsen E et al. Randomized, prospective clinical trial of recombinant factor VIIa for secondary prophylaxis in hemophilia patients with inhibitors. J Thromb Haemost 2007; 5: 1904-13.
-
(2007)
J Thromb Haemost
, vol.5
, pp. 1904-1913
-
-
Konkle, B.A.1
Ebbesen, L.S.2
Erhardtsen, E.3
-
21
-
-
34248562674
-
Prophylactic treatment with activated prothrombin complex concentrate (FEIBA) reduces the frequency of bleeding episodes in paediatric patients with haemophilia A and inhibitors
-
Leissinger CA, Becton DL, Ewing NP, Valentino LA. Prophylactic treatment with activated prothrombin complex concentrate (FEIBA) reduces the frequency of bleeding episodes in paediatric patients with haemophilia A and inhibitors. Haemophilia 2007; 13: 249-55.
-
(2007)
Haemophilia
, vol.13
, pp. 249-255
-
-
Leissinger, C.A.1
Becton, D.L.2
Ewing, N.P.3
Valentino, L.A.4
-
22
-
-
40349100414
-
Recombinant activated factor VII for haemophilia patients with inhibitors undergoing orthopaedic surgery: A review of the literature
-
Obergfell A, Auvinen MK, Mathew P. Recombinant activated factor VII for haemophilia patients with inhibitors undergoing orthopaedic surgery: A review of the literature. Haemophilia 2008; 14: 233-41.
-
(2008)
Haemophilia
, vol.14
, pp. 233-241
-
-
Obergfell, A.1
Auvinen, M.K.2
Mathew, P.3
-
23
-
-
17144437423
-
Home treatment of mild to moderate bleeding episodes using recombinant factor VIIa (Novoseven) in haemophiliacs with inhibitors
-
Key NS, Aledort LM, Beardsley D et al. Home treatment of mild to moderate bleeding episodes using recombinant factor VIIa (Novoseven) in haemophiliacs with inhibitors. Thromb Haemost 1998; 80: 912-8.
-
(1998)
Thromb Haemost
, vol.80
, pp. 912-918
-
-
Key, N.S.1
Aledort, L.M.2
Beardsley, D.3
-
24
-
-
33645750469
-
Home treatment of haemarthroses using a single dose regimen of recombinant activated factor VII in patients with haemophilia and inhibitors. A multi-centre, randomised, double-blind, cross-over trial
-
Kavakli K, Makris M, Bulent Z et al. Home treatment of haemarthroses using a single dose regimen of recombinant activated factor VII in patients with haemophilia and inhibitors. A multi-centre, randomised, double-blind, cross-over trial. Thromb Haemost 2006; 95: 600-5.
-
(2006)
Thromb Haemost
, vol.95
, pp. 600-605
-
-
Kavakli, K.1
Makris, M.2
Bulent, Z.3
-
25
-
-
0019426632
-
The effect of activated prothrombincomplex concentrate (FEIBA) on joint and muscle bleeding in patients with hemophilia A and antibodies to factor VIII. A double-blind clinical trial
-
Sjamsoedin LJ, Heijnen L, Mauser-Bunschoten EP et al. The effect of activated prothrombincomplex concentrate (FEIBA) on joint and muscle bleeding in patients with hemophilia A and antibodies to factor VIII. A double-blind clinical trial. N Engl J Med 1981; 305: 717-21.
-
(1981)
N Engl J Med
, vol.305
, pp. 717-721
-
-
Sjamsoedin, L.J.1
Heijnen, L.2
Mauser-Bunschoten, E.P.3
-
26
-
-
0030837755
-
Multicenter retrospective study on the utilization of FEIBA in France in patients with factor VIII and factor IX inhibitors
-
Negrier C, Goudemand J, Sultan Y et al. Multicenter retrospective study on the utilization of FEIBA in France in patients with factor VIII and factor IX inhibitors. Thromb Haemost 1997; 77: 1113-9.
-
(1997)
Thromb Haemost
, vol.77
, pp. 1113-1119
-
-
Negrier, C.1
Goudemand, J.2
Sultan, Y.3
-
27
-
-
33846185403
-
A randomized comparison of bypassing agents in hemophilia complicated by an inhibitor: The FEIBA NovoSeven Comparative (FENOC) Study
-
Astermark J, Donfield SM, DiMichele DM et al. A randomized comparison of bypassing agents in hemophilia complicated by an inhibitor: The FEIBA NovoSeven Comparative (FENOC) Study. Blood 2007; 109: 546-51.
-
(2007)
Blood
, vol.109
, pp. 546-551
-
-
Astermark, J.1
Donfield, S.M.2
DiMichele, D.M.3
-
28
-
-
33645573977
-
A prospective randomized trial of high and standard dosages of recombinant factor VIIa for treatment of hemarthroses in hemophiliacs with inhibitors
-
Santagostino E, Mancuso ME, Rocino A, Mancuso G, Scaraggi F, Mannucci PM. A prospective randomized trial of high and standard dosages of recombinant factor VIIa for treatment of hemarthroses in hemophiliacs with inhibitors. J Thromb Haemost 2006; 4: 367-71.
-
(2006)
J Thromb Haemost
, vol.4
, pp. 367-371
-
-
Santagostino, E.1
Mancuso, M.E.2
Rocino, A.3
Mancuso, G.4
Scaraggi, F.5
Mannucci, P.M.6
-
29
-
-
40349085780
-
Single 270 microg kg(-1)-dose rFVIIa vs. standard 90 microg kg(-1)-dose rFVIIa and APCC for home treatment of joint bleeds in haemophilia patients with inhibitors: A randomized comparison
-
Young G, Shafer FE, Rojas P, Seremetis S. Single 270 microg kg(-1)-dose rFVIIa vs. standard 90 microg kg(-1)-dose rFVIIa and APCC for home treatment of joint bleeds in haemophilia patients with inhibitors: A randomized comparison. Haemophilia 2008; 14: 287-94.
-
(2008)
Haemophilia
, vol.14
, pp. 287-294
-
-
Young, G.1
Shafer, F.E.2
Rojas, P.3
Seremetis, S.4
-
30
-
-
69949107404
-
-
HemoRec registry web site. Available at: (last accessed on 28 October 2008)
-
HemoRec registry web site. Available at: http://www.hemorec.com (last accessed on 28 October 2008).
-
(2008)
-
-
-
31
-
-
0036862120
-
Prophylactic versus on-demand treatment strategies for severe haemophilia: A comparison of costs and long-term outcome
-
Fischer K, van der Bom JG, Molho P et al. Prophylactic versus on-demand treatment strategies for severe haemophilia: A comparison of costs and long-term outcome. Haemophilia 2002; 8: 745-52.
-
(2002)
Haemophilia
, vol.8
, pp. 745-752
-
-
Fischer, K.1
van der Bom, J.G.2
Molho, P.3
-
32
-
-
0026635406
-
Twenty-five years' experience of prophylactic treatment in severe haemophilia A and B
-
Nilsson IM, Berntorp E, Löfqvist T, Pettersson H. Twenty-five years' experience of prophylactic treatment in severe haemophilia A and B. J Intern Med 1992; 232: 25-32.
-
(1992)
J Intern Med
, vol.232
, pp. 25-32
-
-
Nilsson, I.M.1
Berntorp, E.2
Löfqvist, T.3
Pettersson, H.4
-
33
-
-
0036489589
-
Experience of prophylaxis treatment in children with severe haemophilia
-
Yee TT, Beeton K, Griffioen A et al. Experience of prophylaxis treatment in children with severe haemophilia. Haemophilia 2002; 8: 76-82.
-
(2002)
Haemophilia
, vol.8
, pp. 76-82
-
-
Yee, T.T.1
Beeton, K.2
Griffioen, A.3
-
34
-
-
34547757915
-
Prophylaxis versus episodic treatment to prevent joint disease in boys with severe hemophilia
-
Manco-Johnson MJ, Abshire TC, Shapiro AD et al. Prophylaxis versus episodic treatment to prevent joint disease in boys with severe hemophilia. N Engl J Med 2007; 357: 535-44.
-
(2007)
N Engl J Med
, vol.357
, pp. 535-544
-
-
Manco-Johnson, M.J.1
Abshire, T.C.2
Shapiro, A.D.3
-
35
-
-
53249097439
-
Prevention of haemophilic arthropathy during childhood. May common orthopaedic management be extrapolated from patients without inhibitors to patients with inhibitors?
-
Rodriguez-Merchan EC, Hedner U, Heijnen L et al. Prevention of haemophilic arthropathy during childhood. May common orthopaedic management be extrapolated from patients without inhibitors to patients with inhibitors? Haemophilia 2008; 14(Suppl 6): 68-81.
-
(2008)
Haemophilia
, vol.14
, Issue.SUPPL. 6
, pp. 68-81
-
-
Rodriguez-Merchan, E.C.1
Hedner, U.2
Heijnen, L.3
-
36
-
-
4644334185
-
Prevention of bleeds in hemophilia patients with inhibitors: Emerging data and clinical direction
-
Leissinger CA. Prevention of bleeds in hemophilia patients with inhibitors: Emerging data and clinical direction. Am J Hematol 2004; 77: 187-93.
-
(2004)
Am J Hematol
, vol.77
, pp. 187-193
-
-
Leissinger, C.A.1
-
37
-
-
19444375983
-
Prophylactic recombinant factor VIIa in haemophilia patients with inhibitors
-
Young G, McDaniel M, Nugent DJ. Prophylactic recombinant factor VIIa in haemophilia patients with inhibitors. Haemophilia 2005; 11: 203-7.
-
(2005)
Haemophilia
, vol.11
, pp. 203-207
-
-
Young, G.1
McDaniel, M.2
Nugent, D.J.3
-
38
-
-
34548301664
-
Prophylactic treatment of haemophilia patients with inhibitors: Clinical experience with recombinant factor VIIa in European Haemophilia Centres
-
Morfini M, Auerswald G, Kobelt RA et al. Prophylactic treatment of haemophilia patients with inhibitors: Clinical experience with recombinant factor VIIa in European Haemophilia Centres. Haemophilia 2007; 13: 502-7.
-
(2007)
Haemophilia
, vol.13
, pp. 502-507
-
-
Morfini, M.1
Auerswald, G.2
Kobelt, R.A.3
-
39
-
-
0036210038
-
Clinical outcomes and resource utilization associated with haemophilia care in Europe
-
Schramm W, Royal S, Kroner B et al. Clinical outcomes and resource utilization associated with haemophilia care in Europe. Haemophilia 2002; 8: 33-43.
-
(2002)
Haemophilia
, vol.8
, pp. 33-43
-
-
Schramm, W.1
Royal, S.2
Kroner, B.3
-
40
-
-
43149116111
-
Secondary prophylaxis with recombinant activated factor VII improves health-related quality of life of haemophilia patients with inhibitors
-
Hoots WK, Ebbesen LS, Konkle BA et al. Secondary prophylaxis with recombinant activated factor VII improves health-related quality of life of haemophilia patients with inhibitors. Haemophilia 2008; 14: 466-75.
-
(2008)
Haemophilia
, vol.14
, pp. 466-475
-
-
Hoots, W.K.1
Ebbesen, L.S.2
Konkle, B.A.3
-
41
-
-
34548321383
-
A randomized, double-blind trial demonstrating bioequivalence of the current recombinant activated factor VII formulation and a new robust 25 degrees C stable formulation
-
Bysted BV, Scharling B, Møller T, Hansen BL. A randomized, double-blind trial demonstrating bioequivalence of the current recombinant activated factor VII formulation and a new robust 25 degrees C stable formulation. Haemophilia 2007; 13: 527-32.
-
(2007)
Haemophilia
, vol.13
, pp. 527-532
-
-
Bysted, B.V.1
Scharling, B.2
Møller, T.3
Hansen, B.L.4
|