-
1
-
-
84871011258
-
Guidelines for the management of hemophilia
-
Srivastava A, Brewer AK, Mauser-Bunschoten EP, Key NS, Kitchen S, Llinas A, Ludlam CA, Mahlangu JN, Mulder K, Poon MC, Street A; Treatment Guidelines Working Group on Behalf of the World Federation of Hemophilia. Guidelines for the management of hemophilia. Haemophilia 2013; 19: e1–47.
-
(2013)
Haemophilia
, vol.19
, pp. e1-47
-
-
Srivastava, A.1
Brewer, A.K.2
Mauser-Bunschoten, E.P.3
Key, N.S.4
Kitchen, S.5
Llinas, A.6
Ludlam, C.A.7
Mahlangu, J.N.8
Mulder, K.9
Poon, M.C.10
Street, A.11
-
2
-
-
34548321381
-
Parents of children with haemophilia – a transforming experience
-
Beeton K, Neal D, Watson T, Lee CA. Parents of children with haemophilia – a transforming experience. Haemophilia 2007; 13: 570–9.
-
(2007)
Haemophilia
, vol.13
, pp. 570-579
-
-
Beeton, K.1
Neal, D.2
Watson, T.3
Lee, C.A.4
-
3
-
-
51249087295
-
A survey of adherence to haemophilia therapy in six European countries: results and recommendations
-
De Moerloose P, Urbancik W, Van Den Berg HM, Richards M. A survey of adherence to haemophilia therapy in six European countries: results and recommendations. Haemophilia 2008; 14: 931–8.
-
(2008)
Haemophilia
, vol.14
, pp. 931-938
-
-
De Moerloose, P.1
Urbancik, W.2
Van Den Berg, H.M.3
Richards, M.4
-
4
-
-
84993661361
-
Factor VIII inhibitors in hemophilia A: rationale and latest evidence
-
Witmer C, Young G. Factor VIII inhibitors in hemophilia A: rationale and latest evidence. Ther Adv Hematol 2013; 4: 59–72.
-
(2013)
Ther Adv Hematol
, vol.4
, pp. 59-72
-
-
Witmer, C.1
Young, G.2
-
5
-
-
78651076712
-
The long-term course of factor VIII inhibitors in patients with congenital haemophilia A without immune tolerance induction
-
Caram C, de Souza RG, de Sousa JC, Araújo Pereira T, do Amaral Cerqueira AM, van der Bom JG, Rezende SM. The long-term course of factor VIII inhibitors in patients with congenital haemophilia A without immune tolerance induction. Thromb Haemost 2011; 105: 59–65.
-
(2011)
Thromb Haemost
, vol.105
, pp. 59-65
-
-
Caram, C.1
de Souza, R.G.2
de Sousa, J.C.3
Araújo Pereira, T.4
do Amaral Cerqueira, A.M.5
van der Bom, J.G.6
Rezende, S.M.7
-
6
-
-
84870302675
-
A bispecific antibody to factors IXa and X restores factor VIII hemostatic activity in a hemophilia A model
-
Kitazawa T, Igawa T, Sampei Z, Muto A, Kojima T, Soeda T, Yoshihashi K, Okuyama-Nishida Y, Saito H, Tsunoda H, Suzuki T, Adachi H, Miyazaki T, Ishii S, Kamata-Sakurai M, Iida T, Harada A, Esaki K, Funaki M, Moriyama C, et al. A bispecific antibody to factors IXa and X restores factor VIII hemostatic activity in a hemophilia A model. Nat Med 2012; 18: 1570–4.
-
(2012)
Nat Med
, vol.18
, pp. 1570-1574
-
-
Kitazawa, T.1
Igawa, T.2
Sampei, Z.3
Muto, A.4
Kojima, T.5
Soeda, T.6
Yoshihashi, K.7
Okuyama-Nishida, Y.8
Saito, H.9
Tsunoda, H.10
Suzuki, T.11
Adachi, H.12
Miyazaki, T.13
Ishii, S.14
Kamata-Sakurai, M.15
Iida, T.16
Harada, A.17
Esaki, K.18
Funaki, M.19
Moriyama, C.20
more..
-
7
-
-
85021675727
-
Factor VIIIa-mimetic cofactor activity of a bispecific antibody to factors IX/IXa and X/Xa, emicizumab, depends on its ability to bridge the antigens
-
Kitazawa T, Esaki K, Tachibana T, Ishii S, Soeda T, Muto A, Kawabe Y, Tomoyuki I, Tsunoda H, Nogami K, Shima M, Hattori H. Factor VIIIa-mimetic cofactor activity of a bispecific antibody to factors IX/IXa and X/Xa, emicizumab, depends on its ability to bridge the antigens. Thromb Haemost 2017; 117: 1348–57.
-
(2017)
Thromb Haemost
, vol.117
, pp. 1348-1357
-
-
Kitazawa, T.1
Esaki, K.2
Tachibana, T.3
Ishii, S.4
Soeda, T.5
Muto, A.6
Kawabe, Y.7
Tomoyuki, I.8
Tsunoda, H.9
Nogami, K.10
Shima, M.11
Hattori, H.12
-
8
-
-
84971325206
-
Factor VIII-mimetic function of humanized bispecific antibody in hemophilia A
-
Shima M, Hanabusa H, Taki M, Matsushita T, Sato T, Fukutake K, Fukazawa N, Yoneyama K, Yoshida H, Nogami K. Factor VIII-mimetic function of humanized bispecific antibody in hemophilia A. N Engl J Med 2016; 374: 2044–53.
-
(2016)
N Engl J Med
, vol.374
, pp. 2044-2053
-
-
Shima, M.1
Hanabusa, H.2
Taki, M.3
Matsushita, T.4
Sato, T.5
Fukutake, K.6
Fukazawa, N.7
Yoneyama, K.8
Yoshida, H.9
Nogami, K.10
-
9
-
-
85041670842
-
Long-term safety and efficacy of emicizumab in a phase 1/2 study in hemophilia A patients with or without inhibitors
-
Shima M, Hanabusa H, Taki M, Matsushita T, Sato T, Fukutake K, Kasai R, Yoneyama K, Yoshida H, Nogami K. Long-term safety and efficacy of emicizumab in a phase 1/2 study in hemophilia A patients with or without inhibitors. Blood Advances 2017; 1: 1891–9.
-
(2017)
Blood Advances
, vol.1
, pp. 1891-1899
-
-
Shima, M.1
Hanabusa, H.2
Taki, M.3
Matsushita, T.4
Sato, T.5
Fukutake, K.6
Kasai, R.7
Yoneyama, K.8
Yoshida, H.9
Nogami, K.10
-
10
-
-
85028497303
-
Emicizumab Prophylaxis in Hemophilia A with Inhibitors
-
Oldenburg J, Mahlangu JN, Kim B, Schmitt C, Callaghan MU, Young G, Santagostino E, Kruse-Jarres R, Negrier C, Kessler C, Valente N, Asikanius E, Levy GG, Windyga J, Shima M. Emicizumab Prophylaxis in Hemophilia A with Inhibitors. N Engl J Med 2017; 377: 809–18.
-
(2017)
N Engl J Med
, vol.377
, pp. 809-818
-
-
Oldenburg, J.1
Mahlangu, J.N.2
Kim, B.3
Schmitt, C.4
Callaghan, M.U.5
Young, G.6
Santagostino, E.7
Kruse-Jarres, R.8
Negrier, C.9
Kessler, C.10
Valente, N.11
Asikanius, E.12
Levy, G.G.13
Windyga, J.14
Shima, M.15
-
11
-
-
84963623112
-
A first-in-human phase 1 study of ACE910, a novel factor VIII-mimetic bispecific antibody, in healthy subjects
-
Uchida N, Sambe T, Yoneyama K, Fukazawa N, Kawanishi T, Kobayashi S, Shima M. A first-in-human phase 1 study of ACE910, a novel factor VIII-mimetic bispecific antibody, in healthy subjects. Blood 2016; 127: 1633–41.
-
(2016)
Blood
, vol.127
, pp. 1633-1641
-
-
Uchida, N.1
Sambe, T.2
Yoneyama, K.3
Fukazawa, N.4
Kawanishi, T.5
Kobayashi, S.6
Shima, M.7
-
12
-
-
0030803339
-
Properties of optical data from activated partial thromboplastin time and prothrombin time assays
-
Braun PJ, Givens TB, Stead AG, Beck LR, Gooch SA, Swan RJ, Fischer TJ. Properties of optical data from activated partial thromboplastin time and prothrombin time assays. Thromb Haemost 1997; 78: 1079–87.
-
(1997)
Thromb Haemost
, vol.78
, pp. 1079-1087
-
-
Braun, P.J.1
Givens, T.B.2
Stead, A.G.3
Beck, L.R.4
Gooch, S.A.5
Swan, R.J.6
Fischer, T.J.7
-
13
-
-
84893514460
-
Towards standardization of clot waveform analysis and recommendations for its clinical applications
-
Shima M, Thachil J, Nair SC, Srivastava A. Towards standardization of clot waveform analysis and recommendations for its clinical applications. J Thromb Haemost 2013; 11: 1417–20.
-
(2013)
J Thromb Haemost
, vol.11
, pp. 1417-1420
-
-
Shima, M.1
Thachil, J.2
Nair, S.C.3
Srivastava, A.4
-
14
-
-
44249095589
-
New assays for monitoring haemophilia treatment
-
Shima M, Matsumoto T, Ogiwara K. New assays for monitoring haemophilia treatment. Haemophilia 2008; 14(Suppl. 3): 83–92.
-
(2008)
Haemophilia
, vol.14
, pp. 83-92
-
-
Shima, M.1
Matsumoto, T.2
Ogiwara, K.3
-
15
-
-
0036125865
-
The utility of activated partial thromboplastin time (aPTT) clot waveform analysis in the investigation of hemophilia A patients with very low levels of factor VIII activity (FVIII:C)
-
Shima M, Matsumoto T, Fukuda K, Kubota Y, Tanaka I, Nishiya K, Giles AR, Yoshioka A. The utility of activated partial thromboplastin time (aPTT) clot waveform analysis in the investigation of hemophilia A patients with very low levels of factor VIII activity (FVIII:C). Thromb Haemost 2002; 87: 436–41.
-
(2002)
Thromb Haemost
, vol.87
, pp. 436-441
-
-
Shima, M.1
Matsumoto, T.2
Fukuda, K.3
Kubota, Y.4
Tanaka, I.5
Nishiya, K.6
Giles, A.R.7
Yoshioka, A.8
-
16
-
-
33645582371
-
The measurement of low levels of factor VIII or factor IX in hemophilia A and hemophilia B plasma by clot waveform analysis and thrombin generation assay
-
Matsumoto T, Shima M, Takeyama M, Yoshida K, Tanaka I, Sakurai Y, Giles AR, Yoshioka A. The measurement of low levels of factor VIII or factor IX in hemophilia A and hemophilia B plasma by clot waveform analysis and thrombin generation assay. J Thromb Haemost 2006; 4: 377–84.
-
(2006)
J Thromb Haemost
, vol.4
, pp. 377-384
-
-
Matsumoto, T.1
Shima, M.2
Takeyama, M.3
Yoshida, K.4
Tanaka, I.5
Sakurai, Y.6
Giles, A.R.7
Yoshioka, A.8
-
17
-
-
85026316597
-
Clot waveform analysis using CS-2000i™ distinguishes between very low and absent levels of factor VIII activity in patients with severe hemophilia A
-
Matsumoto T, Nogami K, Tabuchi Y, Yada K, Ogiwara K, Kurono H, Arai N, Shima M. Clot waveform analysis using CS-2000i™ distinguishes between very low and absent levels of factor VIII activity in patients with severe hemophilia A. Haemophilia 2017; 23: e427–35.
-
(2017)
Haemophilia
, vol.23
, pp. e427-e435
-
-
Matsumoto, T.1
Nogami, K.2
Tabuchi, Y.3
Yada, K.4
Ogiwara, K.5
Kurono, H.6
Arai, N.7
Shima, M.8
-
18
-
-
84896767826
-
Optimal monitoring of bypass-therapy in hemophilia A patients with inhibitor using clot waveform analysis
-
Haku J, Nogami K, Matsumoto T, Ogiwara K, Shima M. Optimal monitoring of bypass-therapy in hemophilia A patients with inhibitor using clot waveform analysis. J Thromb Haemost 2014; 12: 355–62.
-
(2014)
J Thromb Haemost
, vol.12
, pp. 355-362
-
-
Haku, J.1
Nogami, K.2
Matsumoto, T.3
Ogiwara, K.4
Shima, M.5
-
19
-
-
84874562364
-
Identification and multidimensional optimization of an asymmetric bispecific IgG antibody mimicking the function of factor VIII cofactor activity
-
Sampei Z, Igawa T, Soeda T, Okuyama-Nishida Y, Moriyama C, Wakabayashi T, Tanaka E, Muto A, Kojima T, Kitazawa T, Yoshihashi K, Harada A, Funaki M, Haraya K, Tachibana T, Suzuki S, Esaki K, Nabuchi Y, Hattori K. Identification and multidimensional optimization of an asymmetric bispecific IgG antibody mimicking the function of factor VIII cofactor activity. PLoS ONE 2013; 8: e57479.
-
(2013)
PLoS ONE
, vol.8
-
-
Sampei, Z.1
Igawa, T.2
Soeda, T.3
Okuyama-Nishida, Y.4
Moriyama, C.5
Wakabayashi, T.6
Tanaka, E.7
Muto, A.8
Kojima, T.9
Kitazawa, T.10
Yoshihashi, K.11
Harada, A.12
Funaki, M.13
Haraya, K.14
Tachibana, T.15
Suzuki, S.16
Esaki, K.17
Nabuchi, Y.18
Hattori, K.19
-
20
-
-
84893537691
-
Anti-factor IXa/X bispecific antibody (ACE910): hemostatic potency against ongoing bleeds in a hemophilia A model and the possibility of routine supplementation
-
Muto A, Yoshihashi K, Takeda M, Kitazawa T, Soeda T, Igawa T, Sakamoto Y, Haraya K, Kawabe Y, Shima M, Yoshioka A, Hattori K. Anti-factor IXa/X bispecific antibody (ACE910): hemostatic potency against ongoing bleeds in a hemophilia A model and the possibility of routine supplementation. J Thromb Haemost 2014; 12: 206–13.
-
(2014)
J Thromb Haemost
, vol.12
, pp. 206-213
-
-
Muto, A.1
Yoshihashi, K.2
Takeda, M.3
Kitazawa, T.4
Soeda, T.5
Igawa, T.6
Sakamoto, Y.7
Haraya, K.8
Kawabe, Y.9
Shima, M.10
Yoshioka, A.11
Hattori, K.12
-
21
-
-
1842678190
-
Remodeling the blood coagulation cascade
-
Hoffman M. Remodeling the blood coagulation cascade. J Thromb Thrombolysis 2003; 16: 17–20.
-
(2003)
J Thromb Thrombolysis
, vol.16
, pp. 17-20
-
-
Hoffman, M.1
-
22
-
-
44649088192
-
Further understanding of recombinant activated factor VII mode of action
-
Monroe DM. Further understanding of recombinant activated factor VII mode of action. Semin Hematol 2008; 45(2 Suppl. 1): S7–11.
-
(2008)
Semin Hematol
, vol.45
, Issue.2
, pp. S7-11
-
-
Monroe, D.M.1
-
24
-
-
79952045233
-
Prevalence, biological phenotype and genotype in moderate/mild hemophilia A with discrepancy between one-stage and chromogenic factor VIII activity
-
Trossaërt M, Boisseau P, Quemener A, Sigaud M, Fouassier M, Ternisien C, Lefrançois-Bettembourg A, Tesson C, Thomas C, Bezieau S. Prevalence, biological phenotype and genotype in moderate/mild hemophilia A with discrepancy between one-stage and chromogenic factor VIII activity. J Thromb Haemost 2011; 9: 524–30.
-
(2011)
J Thromb Haemost
, vol.9
, pp. 524-530
-
-
Trossaërt, M.1
Boisseau, P.2
Quemener, A.3
Sigaud, M.4
Fouassier, M.5
Ternisien, C.6
Lefrançois-Bettembourg, A.7
Tesson, C.8
Thomas, C.9
Bezieau, S.10
-
25
-
-
84946730452
-
Phenotypic heterogeneity of hemostasis in severe hemophilia
-
Nogami K, Shima M. Phenotypic heterogeneity of hemostasis in severe hemophilia. Semin Thromb Hemost 2015; 41: 826–31.
-
(2015)
Semin Thromb Hemost
, vol.41
, pp. 826-831
-
-
Nogami, K.1
Shima, M.2
-
26
-
-
84878666661
-
The mild phenotype in severe hemophilia A with Arg1781His mutation is associated with enhanced binding affinity of factor VIII for factor X
-
Yada K, Nogami K, Wakabayashi H, Fay PJ, Shima M. The mild phenotype in severe hemophilia A with Arg1781His mutation is associated with enhanced binding affinity of factor VIII for factor X. Thromb Haemost 2013; 109: 1007–15.
-
(2013)
Thromb Haemost
, vol.109
, pp. 1007-1015
-
-
Yada, K.1
Nogami, K.2
Wakabayashi, H.3
Fay, P.J.4
Shima, M.5
-
27
-
-
85011068703
-
FVIIIa mimicking bispecific antibody, ACE910 improves in vitro coagulation function of FXI deficiency patient's plasma
-
Minami H, Nogami K, Kitazawa T, Hattori K, Shima M. FVIIIa mimicking bispecific antibody, ACE910 improves in vitro coagulation function of FXI deficiency patient's plasma. J Thromb Haemost 2015; 13(Suppl. 2): 439.
-
(2015)
J Thromb Haemost
, vol.13
, pp. 439
-
-
Minami, H.1
Nogami, K.2
Kitazawa, T.3
Hattori, K.4
Shima, M.5
|