-
1
-
-
0345802754
-
A population based, unselected, consecutive cohort of patients with acquired haemophilia A
-
Collins P, Macartney N, Davies R, Lees S, Giddings J, Majer R. A population based, unselected, consecutive cohort of patients with acquired haemophilia A. Brit J Haematol 2004; 124: 86-90.
-
(2004)
Brit J Haematol
, vol.124
, pp. 86-90
-
-
Collins, P.1
Macartney, N.2
Davies, R.3
Lees, S.4
Giddings, J.5
Majer, R.6
-
2
-
-
33847411624
-
Acquired haemophilia A in the UK: A two year national surveillance study by UK Haemophilia Centre Doctors'Organisation
-
Collins PW, Hirsch S, Baglin TP et al. Acquired haemophilia A in the UK: a two year national surveillance study by UK Haemophilia Centre Doctors'Organisation. Blood 2007; 109: 1870-7.
-
(2007)
Blood
, vol.109
, pp. 1870-1877
-
-
Collins, P.W.1
Hirsch, S.2
Baglin, T.P.3
-
3
-
-
0019501541
-
A survey of 215 non-hemophilic patients with inhibitors to factor VIII
-
Green D, Lechner K. A survey of 215 non-hemophilic patients with inhibitors to factor VIII. Thromb Haemost 1981; 45: 200-3.
-
(1981)
Thromb Haemost
, vol.45
, pp. 200-203
-
-
Green, D.1
Lechner, K.2
-
4
-
-
0027405692
-
Use of porcine factor VIII in the treatment of patients with acquired hemophilia
-
Morrison AE, Ludlam CA, Kessler C. Use of porcine factor VIII in the treatment of patients with acquired hemophilia. Blood 1993; 81: 1513-20.
-
(1993)
Blood
, vol.81
, pp. 1513-1520
-
-
Morrison, A.E.1
Ludlam, C.A.2
Kessler, C.3
-
5
-
-
0030700329
-
The treatment of bleeding in acquired haemophilia with recombinant factor VIIa: A multicentre study
-
Hay CR, Negrier C, Ludlam CA. The treatment of bleeding in acquired haemophilia with recombinant factor VIIa: A multicentre study. Thrombos Haemost 1997; 78: 1463-7.
-
(1997)
Thrombos Haemost
, vol.78
, pp. 1463-1467
-
-
Hay, C.R.1
Negrier, C.2
Ludlam, C.A.3
-
6
-
-
85047693150
-
Acquired hemophilia. A natural history study of 16 patients with factor VIII inhibitors receiving little or no therapy
-
Lottenberg R, Kentro TB, Kitchens CS. Acquired hemophilia. A natural history study of 16 patients with factor VIII inhibitors receiving little or no therapy. Arch Int Med 1987; 147: 1077-81.
-
(1987)
Arch Int Med
, vol.147
, pp. 1077-1081
-
-
Lottenberg, R.1
Kentro, T.B.2
Kitchens, C.S.3
-
7
-
-
33646686129
-
The diagnosis and management of factor VIII and IX inhibitors: A guideline from the United Kingdom Haemophilia Centre Doctors Organisation
-
Hay CRM, Brown SA, 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.M.1
Brown, S.A.2
Collins, P.W.3
Keeling, D.M.4
Liesner, R.5
-
8
-
-
34247876261
-
Treatment of acquired hemophilia A
-
Collins PW. Treatment of acquired hemophilia A. J Thromb Haemost 2007; 5: 893-900.
-
(2007)
J Thromb Haemost
, vol.5
, pp. 893-900
-
-
Collins, P.W.1
-
9
-
-
34548319248
-
Treatment of acquired haemophilia with recombinant activated FVII: A critical appraisal
-
Sumner MJ, Geldziler BD, Pedersen M, Seremetis S. Treatment of acquired haemophilia with recombinant activated FVII: A critical appraisal. Haemophilia 2007; 13: 451-61.
-
(2007)
Haemophilia
, vol.13
, pp. 451-461
-
-
Sumner, M.J.1
Geldziler, B.D.2
Pedersen, M.3
Seremetis, S.4
-
10
-
-
1542360812
-
Treatment of acquired haemophilia with factor eight inhibitor bypassing activity
-
Sallah S. Treatment of acquired haemophilia with factor eight inhibitor bypassing activity. Haemophilia 2004; 10: 169-73.
-
(2004)
Haemophilia
, vol.10
, pp. 169-173
-
-
Sallah, S.1
-
11
-
-
11044234837
-
Activated prothrombin complex concentrate (FEIBA) treatment during surgery in patients with inhibitors to FVIII/IX: The updated Norwegian experience
-
Tjonnfjord GE. Activated prothrombin complex concentrate (FEIBA) treatment during surgery in patients with inhibitors to FVIII/IX: The updated Norwegian experience. Haemophilia 2004; 10(Suppl. 2): 41-5.
-
(2004)
Haemophilia
, vol.10
, Issue.SUPPL. 2
, pp. 41-45
-
-
Tjonnfjord, G.E.1
-
12
-
-
0036489638
-
Safety of factor VIII bypass activity (FEIBA): 10-year compilation of thrombotic adverse events
-
Ehrlich HJ, Henzl MJ, Gomperts ED. Safety of factor VIII bypass activity (FEIBA): 10-year compilation of thrombotic adverse events. Haemophilia 2002; 8: 83-90.
-
(2002)
Haemophilia
, vol.8
, pp. 83-90
-
-
Ehrlich, H.J.1
Henzl, M.J.2
Gomperts, E.D.3
-
13
-
-
3242737794
-
Monitoring the bioavailability of FEIBA with a thrombin generation assay
-
Varadi K, Negrier C, Berntorp E et al. Monitoring the bioavailability of FEIBA with a thrombin generation assay. J Thromb Haemost 2003; 1: 2374-80.
-
(2003)
J Thromb Haemost
, vol.1
, pp. 2374-2380
-
-
Varadi, K.1
Negrier, C.2
Berntorp, E.3
-
14
-
-
4444376084
-
Whole blood clot formation phenotypes in hemophilia A and rare coagulation disorders. Patterns of response to recombinant factor VIIa
-
Sorensen B, Ingerslev J. Whole blood clot formation phenotypes in hemophilia A and rare coagulation disorders. Patterns of response to recombinant factor VIIa. J Thromb Haemost 2004; 2: 102-10.
-
(2004)
J Thromb Haemost
, vol.2
, pp. 102-110
-
-
Sorensen, B.1
Ingerslev, J.2
-
15
-
-
32044441635
-
The modified Bonn Malmo protocol (MBMP) in the treatment of acquired haemophilia A
-
Zeitler H, Ulrich-Merzenich G, Walger P, Dusing R, Vetter H, Brackmann HH. The modified Bonn Malmo protocol (MBMP) in the treatment of acquired haemophilia A. Dtsch Med Wochenschr 2006; 131: 141-7.
-
(2006)
Dtsch Med Wochenschr
, vol.131
, pp. 141-147
-
-
Zeitler, H.1
Ulrich-Merzenich, G.2
Walger, P.3
Dusing, R.4
Vetter, H.5
Brackmann, H.H.6
-
16
-
-
0242608362
-
Immunoadsorption may provide a cost-effective approach to management of patients with inhibitors to FVIII
-
Freedman J, Rand ML, Russell O et al. Immunoadsorption may provide a cost-effective approach to management of patients with inhibitors to FVIII. Transfusion 2003; 43: L508-13.
-
(2003)
Transfusion
, vol.43
-
-
Freedman, J.1
Rand, M.L.2
Russell, O.3
-
17
-
-
0027216670
-
DDAVP in acquired hemophilia A: Case report and review of the literature
-
Mudad R, Kane WH. DDAVP in acquired hemophilia A: Case report and review of the literature. Am J Hematol 1993; 43: 295-9.
-
(1993)
Am J Hematol
, vol.43
, pp. 295-299
-
-
Mudad, R.1
Kane, W.H.2
-
18
-
-
0037394016
-
Acquired haemophilia: Review and meta-analysis focused on therapy and prognostic factors
-
Delgado J, Jimenez-Yuste V, Hernandez-Navarro F, Villar A. Acquired haemophilia: Review and meta-analysis focused on therapy and prognostic factors. Brit J Haematol 2003; 121: 21-35.
-
(2003)
Brit J Haematol
, vol.121
, pp. 21-35
-
-
Delgado, J.1
Jimenez-Yuste, V.2
Hernandez-Navarro, F.3
Villar, A.4
-
19
-
-
0029040859
-
A prospective study of treatment of acquired (autoimmune) factor VIII inhibitors with high-dose intravenous gammaglobulin
-
Schwartz RS, Gabriel DA, Aledort LM, Green D, Kessler CM. A prospective study of treatment of acquired (autoimmune) factor VIII inhibitors with high-dose intravenous gammaglobulin. Blood 1995; 86: 797-804.
-
(1995)
Blood
, vol.86
, pp. 797-804
-
-
Schwartz, R.S.1
Gabriel, D.A.2
Aledort, L.M.3
Green, D.4
Kessler, C.M.5
-
20
-
-
2942591961
-
Selective B-cell depletion with rituximab for the treatment of patients with acquired hemophilia
-
Stasi R, Brunetti M, Stipa E, Amadori S. Selective B-cell depletion with rituximab for the treatment of patients with acquired hemophilia. Blood 2004; 103: 4424-8.
-
(2004)
Blood
, vol.103
, pp. 4424-4428
-
-
Stasi, R.1
Brunetti, M.2
Stipa, E.3
Amadori, S.4
-
21
-
-
33845741137
-
Rituximab for the treatment of patients with very high-titre acquired factor VIII inhibitors refractory to conventional chemotherapy
-
Field JJ, Fenske TS, Blinder MA. Rituximab for the treatment of patients with very high-titre acquired factor VIII inhibitors refractory to conventional chemotherapy. Haemophilia 2007; 13: 46-50.
-
(2007)
Haemophilia
, vol.13
, pp. 46-50
-
-
Field, J.J.1
Fenske, T.S.2
Blinder, M.A.3
-
22
-
-
0033678879
-
New protocol for immune tolerance induction in acquired hemophilia
-
Nemes L, Pitlik E. New protocol for immune tolerance induction in acquired hemophilia. Haematologica 2000; 85(Suppl. 10): 64-8.
-
(2000)
Haematologica
, vol.85
, Issue.SUPPL. 10
, pp. 64-68
-
-
Nemes, L.1
Pitlik, E.2
-
23
-
-
15244340408
-
Treatment of acquired hemophilia by the Bonn-Malmo Protocol: Documentation of an in vivo immunomodulating concept
-
Zeitler H, Ulrich-Merzenich G, Hess L et al. Treatment of acquired hemophilia by the Bonn-Malmo Protocol: Documentation of an in vivo immunomodulating concept. Blood 2005; 105: 2287-93.
-
(2005)
Blood
, vol.105
, pp. 2287-2293
-
-
Zeitler, H.1
Ulrich-Merzenich, G.2
Hess, L.3
-
24
-
-
31444441562
-
Acquired von Willebrand Syndrome: An under- and misdiagnosed bleeding complication in patients with lympho- and myeloproliferative disorders
-
Federici AB. Acquired von Willebrand Syndrome: An under- and misdiagnosed bleeding complication in patients with lympho- and myeloproliferative disorders. Semin Hematol 2006; 43: S48-58.
-
(2006)
Semin Hematol
, vol.43
-
-
Federici, A.B.1
-
25
-
-
0014296886
-
Acquired von Willebrand's syndrome in systemic lupus erythematosus
-
Simone JV, Cornet JA, Abildgaard CF. Acquired von Willebrand's syndrome in systemic lupus erythematosus. Blood 1968; 31: 806-12.
-
(1968)
Blood
, vol.31
, pp. 806-812
-
-
Simone, J.V.1
Cornet, J.A.2
Abildgaard, C.F.3
-
27
-
-
0034911766
-
Acquired von Willebrand syndromes: Clinical features, aetiology, pathophysiology, classification and management
-
Michiels JJ, Budde U, van der Planken M, van Vliet HH, Schroyens W, Berneman Z. Acquired von Willebrand syndromes: Clinical features, aetiology, pathophysiology, classification and management. Best Pract Res Clin Hematol 2001; 14: 401-36.
-
(2001)
Best Pract Res Clin Hematol
, vol.14
, pp. 401-436
-
-
Michiels, J.J.1
Budde, U.2
van der Planken, M.3
van Vliet, H.H.4
Schroyens, W.5
Berneman, Z.6
-
28
-
-
0005579931
-
Subcommittee on von Willebrand Factor: Acquired von Willebrand syndrome: Data from a International Registry
-
Federici AB, Rand JH, Bucciarelli P et al. Subcommittee on von Willebrand Factor: Acquired Don Willebrand syndrome: data from a International Registry. Thromb Haemost 2000; 84: 345-9.
-
(2000)
Thromb Haemost
, vol.84
, pp. 345-349
-
-
Federici, A.B.1
Rand, J.H.2
Bucciarelli, P.3
-
29
-
-
40949125129
-
Diagnostic work-up of patients with acquired von Willebrand syndrome: A retrospective single-center cohort study
-
Tiede A, Priesack J, Werwitze S et al. Diagnostic work-up of patients with acquired von Willebrand syndrome: A retrospective single-center cohort study. J Thromb Haemost 2008; 6: 569-76.
-
(2008)
J Thromb Haemost
, vol.6
, pp. 569-576
-
-
Tiede, A.1
Priesack, J.2
Werwitze, S.3
-
30
-
-
0032525318
-
Clinical significance of inhibitors in acquired von Willebrand syndrome
-
Mohri H, Motomura S, Kanamori H et al. Clinical significance of inhibitors in acquired von Willebrand syndrome. Blood 1998; 91: 3623-9.
-
(1998)
Blood
, vol.91
, pp. 3623-3629
-
-
Mohri, H.1
Motomura, S.2
Kanamori, H.3
-
31
-
-
0029551960
-
Antibodies to von Willebrand factor in von Willebrand disease
-
In: Aledort LM, Hoyer LW, Reisner HM, White GC II, eds. New York: Plenum Press
-
Mannucci PM, Federici AB. Antibodies to von Willebrand factor in von Willebrand disease. In: Aledort LM, Hoyer LW, Reisner HM, White GC II, eds. Inhibitors to Coagulation Factors. New York: Plenum Press, 1995: 87-92.
-
(1995)
Inhibitors to Coagulation Factors
, pp. 87-92
-
-
Mannucci, P.M.1
Federici, A.B.2
-
32
-
-
0038441397
-
A new ELISA assay for diagnosis of acquired von Willebrand Syndrome
-
Siaka C, Rugeri L, Caron C, Goudemand J. A new ELISA assay for diagnosis of acquired von Willebrand Syndrome. Haemophilia 2003; 9: 303-8.
-
(2003)
Haemophilia
, vol.9
, pp. 303-308
-
-
Siaka, C.1
Rugeri, L.2
Caron, C.3
Goudemand, J.4
-
33
-
-
0032532314
-
Treatment of acquired von Willebrand syndrome in patients with monoclonal gammopathy of uncertain significance: Comparison of three different therapeutic approaches
-
Federici AB, Stabile F, Castaman G, Canciani MT, Mannucci PM. Treatment of acquired von Willebrand syndrome in patients with monoclonal gammopathy of uncertain significance: Comparison of three different therapeutic approaches. Blood 1998; 92: 2707-11.
-
(1998)
Blood
, vol.92
, pp. 2707-2711
-
-
Federici, A.B.1
Stabile, F.2
Castaman, G.3
Canciani, M.T.4
Mannucci, P.M.5
-
34
-
-
0035095715
-
Successful treatment with recombinant factor VIIa of therapy-resistant severe bleeding in a patient with acquired von Willebrand disease
-
Friederich PW, Wever PC, Briet E, Doorenbos CJ, Levi M. Successful treatment with recombinant factor VIIa of therapy-resistant severe bleeding in a patient with acquired von Willebrand disease. Am J Hematol 2001; 66: 292-4.
-
(2001)
Am J Hematol
, vol.66
, pp. 292-294
-
-
Friederich, P.W.1
Wever, P.C.2
Briet, E.3
Doorenbos, C.J.4
Levi, M.5
|