-
1
-
-
76149093682
-
Laboratory identification of factor inhibitors: The perspective of a large tertiary hemophilia center
-
Kershaw G, Jayakodi D, Dunkley S. Laboratory identification of factor inhibitors: the perspective of a large tertiary hemophilia center. Semin Thromb Hemost 2009; 35: 760-8.
-
(2009)
Semin Thromb Hemost
, vol.35
, pp. 760-768
-
-
Kershaw, G.1
Jayakodi, D.2
Dunkley, S.3
-
3
-
-
33751040152
-
Inhibitor treatment in haemophilias A and B: Inhibitor diagnosis
-
DOI 10.1111/j.1365-2516.2006.01364.x
-
Dimichele D. Inhibitor treatment in haemophilias A and B: inhibitor diagnosis. Haemophilia 2006; 12 (Suppl 6): 37-42. (Pubitemid 44752488)
-
(2006)
Haemophilia
, vol.12
, Issue.SUPPL. 6
, pp. 37-42
-
-
Dimichele, D.M.1
-
4
-
-
28344447401
-
Cellular immune responses in hemophilia: Why do inhibitors develop in some, but not all hemophiliacs?
-
DOI 10.1111/j.1538-7836.2005.01375.x
-
White GC, Kempton CL, Grimsley A, Nielsen B, Roberts HR. Cellular immune responses in hemophilia: why do inhibitors develop in some, but not all hemophiliacs? J Thromb Haemost 2005; 3: 1676-81. (Pubitemid 41716553)
-
(2005)
Journal of Thrombosis and Haemostasis
, vol.3
, Issue.8
, pp. 1676-1681
-
-
White II, G.C.1
Kempton, C.L.2
Grimsley, A.3
Nielsen, B.4
Roberts, H.R.5
-
5
-
-
77449116760
-
The multifactorial etiology of inhibitor development in hemophilia: Genetics and environment
-
Gouw SC, van den Berg HM. The multifactorial etiology of inhibitor development in hemophilia: genetics and environment. Semin Thromb Hemost 2009; 35: 723-34.
-
(2009)
Semin Thromb Hemost
, vol.35
, pp. 723-734
-
-
Gouw, S.C.1
Van Den Berg, H.M.2
-
6
-
-
77449091890
-
Inhibitors in hemophilia A: Advances in elucidation of inhibitory mechanisms and in inhibitor management with bypassing agents
-
Ananyeva NM, Lee TK, Jain N, Shima M, Saenko EL. Inhibitors in hemophilia A: advances in elucidation of inhibitory mechanisms and in inhibitor management with bypassing agents. Semin Thromb Hemost 2009; 35: 735-51.
-
(2009)
Semin Thromb Hemost
, vol.35
, pp. 735-751
-
-
Ananyeva, N.M.1
Lee, T.K.2
Jain, N.3
Shima, M.4
Saenko, E.L.5
-
7
-
-
9144232123
-
Inhibitors in congenital coagulation disorders
-
DOI 10.1111/j.1365-2141.2004.05168.x
-
Key NS. Inhibitors in congenital coagulation disorders. Br J Haematol 2004; 127: 379-91. (Pubitemid 39539246)
-
(2004)
British Journal of Haematology
, vol.127
, Issue.4
, pp. 379-391
-
-
Key, N.S.1
-
8
-
-
23844533263
-
Comparative measurement of anti-factor VIII antibody by Bethesda assay and ELISA reveals restricted isotype profile and epitope specificity
-
DOI 10.1159/000086580
-
Towfighi F, Gharagozlou S, Sharifian RA, et al. Comparative measurement of anti-factor VIII antibody by Bethesda assay and ELISA reveals restricted isotype profile and epitope specificity. Acta Haematol 2005; 114: 84-90. (Pubitemid 41160935)
-
(2005)
Acta Haematologica
, vol.114
, Issue.2
, pp. 84-90
-
-
Towfighi, F.1
Gharagozlou, S.2
Sharifian, R.A.3
Kazemnejad, A.4
Esmailzadeh, K.5
Managhchi, M.R.6
Shokri, F.7
-
9
-
-
33750302875
-
Inhibitors to factor VIII-molecular basis
-
Lee C, Berntorp E, Hoots KW, editors Oxford: Blackwell Publishing
-
Oldenburg J, Tuddenham E. Inhibitors to factor VIII-molecular basis. In: Lee C, Berntorp E, Hoots KW, editors. Textbook of Hemophilia. Oxford: Blackwell Publishing, 2005; 59-63.
-
(2005)
Textbook of Hemophilia
, pp. 59-63
-
-
Oldenburg, J.1
Tuddenham, E.2
-
10
-
-
31444453462
-
Natural history of inhibitor development in children with severe hemophilia A treated with FVIII products
-
Lee C, Berntorp E, Hoots KW, editors Oxford: Blackwell Publishing
-
Lusher J. Natural history of inhibitor development in children with severe hemophilia A treated with FVIII products. In: Lee C, Berntorp E, Hoots KW, editors. Textbook of Hemophilia. Oxford: Blackwell Publishing, 2005; 34-8.
-
(2005)
Textbook of Hemophilia
, pp. 34-38
-
-
Lusher, J.1
-
11
-
-
34250708408
-
Treatment characteristics and the risk of inhibitor development: A multicenter cohort study among previously untreated patients with severe hemophilia A
-
DOI 10.1111/j.1538-7836.2007.02595.x
-
Gouw SC, Berg HMVD, Cessie SL, Bom JGVD. Treatment characteristics and the risk of inhibitor development: a multicenter cohort study among previously untreated patients with severe hemophilia A. J Thromb Haemost 2007; 5: 1383-90. (Pubitemid 46965364)
-
(2007)
Journal of Thrombosis and Haemostasis
, vol.5
, Issue.7
, pp. 1383-1390
-
-
Gouw, S.C.1
Van Den Berg, H.M.2
Le Cessie, S.3
Van Der Bom, J.G.4
-
12
-
-
33646146198
-
Laboratory issues in bleeding disorders
-
Lillicrap D, Nair SC, Srivastava A, Rodeghiero F, Pabinger I, Federici AB. Laboratory issues in bleeding disorders. Haemophilia 2006; 12 (Suppl 3): 68-75.
-
(2006)
Haemophilia
, vol.12
, Issue.SUPPL. 3
, pp. 68-75
-
-
Lillicrap, D.1
Nair, S.C.2
Srivastava, A.3
Rodeghiero, F.4
Pabinger, I.5
Federici, A.B.6
-
13
-
-
33750693405
-
Rituximab treatment of mild haemophilia A with inhibitors: A proposed treatment protocol
-
DOI 10.1111/j.1365-2516.2006.01351.x
-
Dunkley S, Kershaw G, Young G, et al. Rituximab treatment of mild haemophilia Awith inhibitors: a proposed treatment protocol. Haemophilia 2006; 12: 663-7. (Pubitemid 44697539)
-
(2006)
Haemophilia
, vol.12
, Issue.6
, pp. 663-667
-
-
Dunkley, S.1
Kershaw, G.2
Young, G.3
Warburton, P.4
Lindeman, R.5
Matthews, S.6
Rennisson, F.7
-
16
-
-
0022480010
-
Acquired inhibitors of plasma coagulation factors
-
Kasper CK, Ewing NP. Acquired inhibitors of plasma coagulation factors. J Med Technol 1986; 38: 431-9. (Pubitemid 16073720)
-
(1986)
Journal of Medical Technology
, vol.3
, Issue.8
, pp. 431-439
-
-
Kasper, C.K.1
Ewing, N.P.2
-
17
-
-
66349115640
-
Autoimmune hemophilia at rescue
-
Mannucci PM, Payvandi F. Autoimmune hemophilia at rescue. Haematologica 2009; 94: 459-61.
-
(2009)
Haematologica
, vol.94
, pp. 459-461
-
-
Mannucci, P.M.1
Payvandi, F.2
-
18
-
-
33847411624
-
Acquired hemophilia A in the United Kingdom: A 2-year national surveillance study by the United Kingdom Haemophilia Centre Doctors' organisation
-
DOI 10.1182/blood-2006-06-029850
-
Collins PW, Hirsch S, Baglin TP, et al. UK Haemophilia Centre Doctors' Organisation Acquired hemophilia A in the United Kingdom: a 2-year national surveillance study by the United Kingdom Haemophilia Centre Doctors' Organisation. Blood 2007; 109: 1870-7. (Pubitemid 46348182)
-
(2007)
Blood
, vol.109
, Issue.5
, pp. 1870-1877
-
-
Collins, P.W.1
Hirsch, S.2
Baglin, T.P.3
Dolan, G.4
Hanley, J.5
Makris, M.6
Keeling, D.M.7
Liesner, R.8
Brown, S.A.9
Hay, C.R.M.10
-
19
-
-
77449132898
-
Twelve years of experience of acquired hemophilia A: Trials and tribulations in south Australia
-
Tay L, Duncan E, Singhal D, et al. Twelve years of experience of acquired hemophilia A: trials and tribulations in south Australia. Semin Thromb Hemost 2009; 35: 769-77.
-
(2009)
Semin Thromb Hemost
, vol.35
, pp. 769-777
-
-
Tay, L.1
Duncan, E.2
Singhal, D.3
-
20
-
-
0019501541
-
A survey of 215 non-hemophilic patients with inhibitors to factor VIII
-
Green D, Lechner K. A survey of 215 non-hemophiliac patients with inhibitors to factor VIII. Thromb Haemost 1981; 45: 200-3. (Pubitemid 11081028)
-
(1981)
Thrombosis and Haemostasis
, vol.45
, Issue.3
, pp. 200-203
-
-
Green, D.1
Lechner, K.2
-
21
-
-
31444452280
-
Inhibitors in hemophilia B
-
Lee C, Berntorp E, Hoots KW, editors Oxford: Blackwell Publishing
-
Warrier I. Inhibitors in hemophilia B. In: Lee C, Berntorp E, Hoots KW, editors. Textbook of Hemophilia. Oxford: Blackwell Publishing, 2005.
-
(2005)
Textbook of Hemophilia
-
-
Warrier, I.1
-
22
-
-
0035022048
-
Haemophilia B mutations in Sweden: A population-based study of mutational heterogeneity
-
DOI 10.1046/j.1365-2141.2001.02759.x
-
Llung R, Petrini P, Tengborn L, Sjorin E. Haemophilia B mutations in Sweden: a population-based study of mutational heterogeneity. Br J Haemat 2001; 113: 81-6. (Pubitemid 32423306)
-
(2001)
British Journal of Haematology
, vol.113
, Issue.1
, pp. 81-86
-
-
Ljung, R.1
Petrini, P.2
Tengborn, L.3
Sjorin, E.4
-
23
-
-
34447123490
-
Treatment of inhibitors in hemophilia B
-
Lee C, Berntorp E, Hoots KW, editors Oxford: Blackwell Publishing
-
Brown SA. Treatment of inhibitors in hemophilia B. In: Lee C, Berntorp E, Hoots KW, editors. Textbook of Hemophilia. Oxford: Blackwell Publishing, 2005; 101-5.
-
(2005)
Textbook of Hemophilia
, pp. 101-105
-
-
Brown, S.A.1
-
24
-
-
10044252189
-
Factor V inhibitors: Rare or not so uncommon? A multi-laboratory investigation
-
DOI 10.1097/00001721-200412000-00003
-
Favaloro EJ, Posen J, Ramakrishna R, et al. Factor V inhibitors: rare or not so uncommon? A multilaboratory investigation. Blood Coag Fibrinolysis 2004; 15: 637-47. (Pubitemid 39612969)
-
(2004)
Blood Coagulation and Fibrinolysis
, vol.15
, Issue.8
, pp. 637-647
-
-
Favaloro, E.J.1
Posen, J.2
Ramakrishna, R.3
Soltani, S.4
McRae, S.5
Just, S.6
Aboud, M.7
Low, J.8
Gemmell, R.9
Kershaw, G.10
Coleman, R.11
Dean, M.12
-
25
-
-
66149179129
-
Acquired factor Vinhibitor. A problem based systematic review
-
Ang AL, Kuperan P, Ng CH, Ng HJ. Acquired factor Vinhibitor. A problem based systematic review. Thromb Haemost 2009; 101: 852-9.
-
(2009)
Thromb Haemost
, vol.101
, pp. 852-859
-
-
Ang, A.L.1
Kuperan, P.2
Ng, C.H.3
Ng, H.J.4
-
26
-
-
79955071646
-
Inherited and acquired factor V deficiency
-
Lippi G, Favaloro EJ, Montagnana M, Manzato F, Guidi GC, Franchini M. Inherited and acquired factor V deficiency. Blood Coag Fibrinolysis 2011; 22: 160-6.
-
(2011)
Blood Coag Fibrinolysis
, vol.22
, pp. 160-166
-
-
Lippi, G.1
Favaloro, E.J.2
Montagnana, M.3
Manzato, F.4
Guidi, G.C.5
Franchini, M.6
-
35
-
-
85171928518
-
Acquired von Willebrand Disease: Potential contribution of the VWF: CB to the identification of functionally inhibiting auto-antibodies to von Willebrand factor
-
Coleman R, Favaloro EJ, Soltani S, Keng TB. Acquired von Willebrand Disease: Potential contribution of the VWF: CB to the identification of functionally inhibiting auto-antibodies to von Willebrand factor. J Thromb Haemost 2008; 4: 1051-2.
-
(2008)
J Thromb Haemost
, vol.4
, pp. 1051-1052
-
-
Coleman, R.1
Favaloro, E.J.2
Soltani, S.3
Keng, T.B.4
-
36
-
-
52449098463
-
Clinical and molecular markers of inherited von Willebrand disease type 3: Are deletions of the VWF gene associated with alloantibodies to VWF?
-
Federici AB. Clinical and molecular markers of inherited von Willebrand disease type 3: are deletions of the VWF gene associated with alloantibodies to VWF? J Thromb Haemost 2008; 6: 1726-8.
-
(2008)
J Thromb Haemost
, vol.6
, pp. 1726-1728
-
-
Federici, A.B.1
-
38
-
-
77953862089
-
Laboratory testing in disseminated intravascular coagulation
-
Favaloro EJ. Laboratory testing in disseminated intravascular coagulation. Semin Thromb Hemost 2010; 36: 458-67.
-
(2010)
Semin Thromb Hemost
, vol.36
, pp. 458-467
-
-
Favaloro, E.J.1
-
39
-
-
53049091449
-
Laboratory testing for lupus anticoagulants: Diagnostic criteria and use of screening, mixing, and confirmatory studies
-
Tripodi A. Laboratory testing for lupus anticoagulants: diagnostic criteria and use of screening, mixing, and confirmatory studies. Semin Thromb Hemost 2008; 34: 373-8.
-
(2008)
Semin Thromb Hemost
, vol.34
, pp. 373-378
-
-
Tripodi, A.1
-
40
-
-
34247860294
-
Acquired inhibitors to factor VIII
-
Lee C, Berntorp E, Hoots KW, editors Oxford: Blackwell Publishing
-
Kessler C, Asatiani E. Acquired inhibitors to factor VIII. In: Lee C, Berntorp E, Hoots KW, editors. Textbook of Hemophilia. Oxford: Blackwell Publishing, 2005; 86-90.
-
(2005)
Textbook of Hemophilia
, pp. 86-90
-
-
Kessler, C.1
Asatiani, E.2
-
41
-
-
0017387653
-
Detection of factor VIII inhibitors with the partial thromboplastin time
-
Lossing T, Kasper C, Feinstein D. Detection of factor VIII inhibitors with the partial thromboplastin time. Blood 1977; 49: 793-7. (Pubitemid 8093475)
-
(1977)
Blood
, vol.49
, Issue.5
, pp. 793-797
-
-
Lossing, T.S.1
Kasper, C.K.2
Feinstein, D.I.3
-
42
-
-
0031797696
-
Acquired haemophilia A: Errors in the diagnosis
-
Kazmi MA, Pickering W, Smith MP, Holland LJ, Savidge GF. Acquired haemophilia A: errors in the diagnosis. Blood Coagul Fibronolysis 1998; 9: 623-8. (Pubitemid 28520160)
-
(1998)
Blood Coagulation and Fibrinolysis
, vol.9
, Issue.7
, pp. 623-628
-
-
Kazmi, M.A.1
Pickering, W.2
Smith, M.P.3
Holland, L.J.4
Savidge, G.F.5
-
43
-
-
78650012663
-
Laboratory investigation of lupus anticoagulants: Mixing studies are sometimes required
-
Favaloro EJ, Bonar R, Zebeljan D, Kershaw G, Marsden K. Laboratory investigation of lupus anticoagulants: mixing studies are sometimes required. J Thromb Haemost 2010; 8: 2828-31.
-
(2010)
J Thromb Haemost
, vol.8
, pp. 2828-2831
-
-
Favaloro, E.J.1
Bonar, R.2
Zebeljan, D.3
Kershaw, G.4
Marsden, K.5
-
44
-
-
84861342503
-
Evaluating laboratory approaches to the identification of lupus anticoagulants: A diagnostic challenge from the RCPA Haematology QAP
-
Bonar R, Favaloro EJ, Zebeljan D, et al. Evaluating laboratory approaches to the identification of lupus anticoagulants: A diagnostic challenge from the RCPA Haematology QAP. Pathology 2012; 44: 240-7.
-
(2012)
Pathology
, vol.44
, pp. 240-247
-
-
Bonar, R.1
Favaloro, E.J.2
Zebeljan, D.3
-
45
-
-
77449096331
-
The between-laboratory variation of factor VIII inhibitor testing: The experience of the external quality assessment program of the ECAT foundation
-
Meijer P, Verbruggen B. The between-laboratory variation of factor VIII inhibitor testing: the experience of the external quality assessment program of the ECAT foundation. Semin Thromb Hemost 2009; 35: 786-93.
-
(2009)
Semin Thromb Hemost
, vol.35
, pp. 786-793
-
-
Meijer, P.1
Verbruggen, B.2
-
47
-
-
0028837315
-
The Nijmegen modification of the Bethesda assay for factor VIII: C inhibitors: Improved specificity and reliability
-
Verbruggen B, Novakova I, Wessels H, Boezeman J, van den Berg M, Mauser-Bunschoten E. The Nijmegen modification of the Bethesda assay for factor VIII: C inhibitors: improved specificity and reliability. Thromb Haemost 1995; 73: 247-51.
-
(1995)
Thromb Haemost
, vol.73
, pp. 247-251
-
-
Verbruggen, B.1
Novakova, I.2
Wessels, H.3
Boezeman, J.4
Van Den Berg, M.5
Mauser-Bunschoten, E.6
-
48
-
-
18344405441
-
A detailed comparison of the performance of the standard versus the Nijmegen modification of the Bethesda assay in detecting Factor VIII:C inhibitors in the haemophilia A population of Canada
-
Giles AR, Verbruggen B, Rivard GE, Teitel J, Walker I. A detailed comparison of the performance of the standard versus the Nijmegen modification of the Bethesda assay in detecting factor VIII: C inhibitors in the haemophilia A population of Canada. Thromb Haemost 1998; 79: 872-5. (Pubitemid 28163870)
-
(1998)
Thrombosis and Haemostasis
, vol.79
, Issue.4
, pp. 872-875
-
-
Giles, A.R.1
Verbruggen, B.2
Rivard, G.E.3
Teitel, J.4
Walker, I.5
Growe, G.6
Poon, M.-C.7
Wu, J.8
Card, R.9
Ali, K.10
Israels, S.11
Rubinger, M.12
Herst, J.13
Gill, K.14
Inwood, M.15
McCusker, P.J.16
Pai, M.17
Garvey, B.18
Blanchette, V.19
Giles, A.20
Lillicrap, D.21
Silva, M.22
Drouin, J.23
Luke, K.-H.24
Bond, M.25
David, M.26
Rivard, G.27
St-Louis, J.28
Lepine-Martin, M.29
Demers, C.30
Jobin, F.31
Scully, M.-F.32
Dolan, S.33
Rubin, S.34
Barnard, D.35
Robinson, S.36
Ross, E.37
Jardine, L.38
more..
-
49
-
-
0036332155
-
A 4% solution of bovine serum albumin may be used in place of factor VII:C deficient plasma in the control sample in the Nijmegen modification of the Bethesda factor VIII:C inhibitor assay
-
Verbruggen B, van Heerde W, Novákovà I, Lillicrap D, Giles A. A 4% solution of bovine serum albumin may be used in place of factor VIII: C deficient plasma in the control sample in the Nijmegen Modification of the Bethesda factor VIII: C inhibitor assay. Thromb Haemost 2002; 88: 362-4. (Pubitemid 34873724)
-
(2002)
Thrombosis and Haemostasis
, vol.88
, Issue.2
, pp. 362-364
-
-
Verbruggen, B.1
Van Heerde, W.2
Novakova, I.3
Lillicrap, D.4
Giles, A.5
-
51
-
-
0024271310
-
Modification of the Bethesda assay for factor FVIII or IX inhibitors to improve efficiency
-
Gadarowski JJ, Czapek EE, Ontiveros JD, Pedraza JL. Modification of the Bethesda assay for factor FVIII or IX inhibitors to improve efficiency. Acta Haematol 1998; 80: 134-8.
-
(1998)
Acta Haematol
, vol.80
, pp. 134-138
-
-
Gadarowski, J.J.1
Czapek, E.E.2
Ontiveros, J.D.3
Pedraza, J.L.4
-
52
-
-
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. (Pubitemid 36622033)
-
(2003)
Haemophilia
, vol.9
, Issue.3
, pp. 303-308
-
-
Siaka, C.1
Rugeri, L.2
Caron, C.3
Goudemand, J.4
-
53
-
-
43749102064
-
Acquired von Willebrand disease: Potential contribution of the von Willebrand factor collagen-binding to the identification of functionally inhibiting auto-antibodies to von Willebrand factor: A rebuttal
-
DOI 10.1111/j.1538-7836.2008.02967.x
-
Guerin V, Ryman A, Velez F. Acquired von Willebrand disease: potential contribution of the von Willebrand factor collagen-binding to the identification of functionally inhibiting auto-antibodies to von Willebrand factor: a rebuttal. J Thromb Haemost 2008; 6: 1051-2. (Pubitemid 351689936)
-
(2008)
Journal of Thrombosis and Haemostasis
, vol.6
, Issue.6
, pp. 1051-1052
-
-
Guerin, V.1
Ryman, A.2
Velez, F.3
-
54
-
-
33746699562
-
Identification of factor inhibitors by diagnostic haemostasis laboratories: A large multi-centre evaluation
-
DOI 10.1160/TH06-01-0004
-
Favaloro EJ, Bonar R, Duncan E, et al. (on behalf of the RCPA QAP in Haematology Haemostasis Committee)Identification of factor inhibitors by diagnostic haemostasis laboratories: A large multi-centre evaluation. Thromb Haemost 2006; 96: 73-8. (Pubitemid 44160873)
-
(2006)
Thrombosis and Haemostasis
, vol.96
, Issue.1
, pp. 73-78
-
-
Favaloro, E.J.1
Bonar, R.2
Duncan, E.3
Earl, G.4
Low, J.5
Aboud, M.6
Just, S.7
Sioufi, J.8
Street, A.9
Marsden, K.10
-
55
-
-
34648816828
-
Mis-identification of factor inhibitors by diagnostic haemostasis laboratories: Recognition of pitfalls and elucidation of strategies. A follow up to a large multicentre evaluation
-
DOI 10.1080/00313020701569998, PII 782040329
-
Favaloro EJ, Bonar R, Duncan E, et al. (on behalf of the RCPA QAP in Haematology Haemostasis Committee). Mis-identification of factor inhibitors by diagnostic haemostasis laboratories: recognition of pitfalls and elucidation of strategies. A follow up to a large multicentre evaluation. Pathology 2007; 39: 504-11. (Pubitemid 47454494)
-
(2007)
Pathology
, vol.39
, Issue.5
, pp. 504-511
-
-
Favaloro, E.J.1
Bonar, R.2
Duncan, E.3
Earl, G.4
Low, J.5
Aboud, M.6
Just, S.7
Sioufi, J.8
Street, A.9
Marsden, K.10
-
56
-
-
77449099048
-
Investigations from external quality assurance programs reveal a high degree of variation in the laboratory identification of coagulation factor inhibitors
-
(on behalf RCPA Haematology QAP Haemostasis Committee)
-
Favaloro EJ, Bonar R, Kershaw G, Duncan E, Sioufi J, Marsden K (on behalf RCPA Haematology QAP Haemostasis Committee). Investigations from external quality assurance programs reveal a high degree of variation in the laboratory identification of coagulation factor inhibitors. Semin Thromb Hemost 2009; 35: 794-805.
-
(2009)
Semin Thromb Hemost
, vol.35
, pp. 794-805
-
-
Favaloro, E.J.1
Bonar, R.2
Kershaw, G.3
Duncan, E.4
Sioufi, J.5
Marsden, K.6
-
57
-
-
77449093450
-
Laboratory identification of factor VIII inhibitors in the real world: The experience from Australasia
-
(on behalf RCPA Haematology QAP Haemostasis Committee)
-
Favaloro EJ, Bonar R, Kershaw G, Mohammed S, Duncan E, Marsden K (on behalf RCPA Haematology QAP Haemostasis Committee). Laboratory identification of factor VIII inhibitors in the real world: the experience from Australasia. Haemophilia 2010; 16: 662-70.
-
(2010)
Haemophilia
, vol.16
, pp. 662-670
-
-
Favaloro, E.J.1
Bonar, R.2
Kershaw, G.3
Mohammed, S.4
Duncan, E.5
Marsden, K.6
-
58
-
-
77449158822
-
Interlaboratory variation in factor VIII: C inhibitor assay results is sufficient to influence patient management: Data from the UK national quality external assessment scheme for blood coagulation
-
Kitchen S, Jennings I, Preston FE, Kitchen DP, Woods TA, Walker ID. Interlaboratory variation in factor VIII: C inhibitor assay results is sufficient to influence patient management: data from the UK national quality external assessment scheme for blood coagulation. Semin Thromb Hemost 2009; 35: 778-85.
-
(2009)
Semin Thromb Hemost
, vol.35
, pp. 778-785
-
-
Kitchen, S.1
Jennings, I.2
Preston, F.E.3
Kitchen, D.P.4
Woods, T.A.5
Walker, I.D.6
-
59
-
-
65349196134
-
Laboratory assessment of factor VIII inhibitor titer: The North American Specialized Coagulation Laboratory Association experience
-
NASCOLA Proficiency Testing Committee
-
Peerschke EI, Castellone DD, Ledford-Kraemer M, Van Cott EM, Meijer P; NASCOLA Proficiency Testing Committee. Laboratory assessment of factor VIII inhibitor titer: the North American Specialized Coagulation Laboratory Association experience. Am J Clin Pathol 2009; 131: 552-8.
-
(2009)
Am J Clin Pathol
, vol.131
, pp. 552-558
-
-
Peerschke, E.I.1
Castellone, D.D.2
Ledford-Kraemer, M.3
Van Cott, E.M.4
Meijer, P.5
-
60
-
-
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. (Pubitemid 36874391)
-
(2003)
Haemophilia
, vol.9
, Issue.4
, pp. 418-435
-
-
Wight, J.1
Paisley, S.2
-
61
-
-
77954506432
-
Rate of inhibitor development in previously untreated hemophilia A patients treated with plasma-derived or recombinant factor VIII concentrates: A systematic review
-
Iorio A, Halimeh S, Holzhauer S, et al. Rate of inhibitor development in previously untreated hemophilia A patients treated with plasma-derived or recombinant factor VIII concentrates: a systematic review. J Thromb Haemost 2010; 8: 1256-65.
-
(2010)
J Thromb Haemost
, vol.8
, pp. 1256-1265
-
-
Iorio, A.1
Halimeh, S.2
Holzhauer, S.3
-
62
-
-
78149492011
-
Von Willebrand factor-containing factor VIII concentrates and inhibitors in haemophilia A. A critical literature review
-
Franchini M, Lippi G. Von Willebrand factor-containing factor VIII concentrates and inhibitors in haemophilia A. A critical literature review. Thromb Haemost 2010; 104: 931-40.
-
(2010)
Thromb Haemost
, vol.104
, pp. 931-940
-
-
Franchini, M.1
Lippi, G.2
-
63
-
-
84855912746
-
Cumulative inhibitor incidence in previously untreated patients with severe hemophilia A treated with plasma-derived versus recombinant factor VIII concentrates: A critical systematic review
-
Franchini M, Tagliaferri A, Mengoli C, Cruciani M. Cumulative inhibitor incidence in previously untreated patients with severe hemophilia A treated with plasma-derived versus recombinant factor VIII concentrates: A critical systematic review. Crit Rev Oncol Hematol 2012; 81: 82-93.
-
(2012)
Crit Rev Oncol Hematol
, vol.81
, pp. 82-93
-
-
Franchini, M.1
Tagliaferri, A.2
Mengoli, C.3
Cruciani, M.4
-
64
-
-
78049285843
-
Plasma-derived versus recombinant factor VIII concentrates for the treatment of haemophilia A: Plasma-derived is better
-
Mannucci PM. Plasma-derived versus recombinant factor VIII concentrates for the treatment of haemophilia A: plasma-derived is better. Blood Transfus 2010; 8: 288-91.
-
(2010)
Blood Transfus
, vol.8
, pp. 288-291
-
-
Mannucci, P.M.1
-
65
-
-
78049271862
-
Plasma-derived versus recombinant Factor VIII concentrates for the treatment of haemophilia A: Recombinant is better
-
Franchini M. Plasma-derived versus recombinant Factor VIII concentrates for the treatment of haemophilia A: recombinant is better. Blood Transfus 2010; 8: 292-6.
-
(2010)
Blood Transfus
, vol.8
, pp. 292-296
-
-
Franchini, M.1
-
66
-
-
79959529406
-
Recombinant factor concentrates may increase inhibitor development: A single centre cohort study
-
Strauss T, Lubetsky A, Ravid B, et al. Recombinant factor concentrates may increase inhibitor development: a single centre cohort study. Haemophilia 2011; 17: 625-9.
-
(2011)
Haemophilia
, vol.17
, pp. 625-629
-
-
Strauss, T.1
Lubetsky, A.2
Ravid, B.3
-
67
-
-
80055114308
-
Can B-domain deletion alter the immunogenicity of recombinant factor VIII? A meta-analysis of prospective clinical studies
-
Aledort LM, Navickis RJ, Wilkes MM. Can B-domain deletion alter the immunogenicity of recombinant factor VIII? A meta-analysis of prospective clinical studies. J Thromb Haemost 2011; 9: 2180-92.
-
(2011)
J Thromb Haemost
, vol.9
, pp. 2180-2192
-
-
Aledort, L.M.1
Navickis, R.J.2
Wilkes, M.M.3
|