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Hybrid human‐porcine factor VIII proteins partially escape the inhibitory effects of anti‐factor VIII inhibitor alloantibodies having A2 or C2 domain specificity.
- Published in:
- Haemophilia, 2024, v. 30, n. 1, p. 140, doi. 10.1111/hae.14911
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- Publication type:
- Article
Coagulation potentials of plasma‐derived factors VIIa and X mixture (Byclot<sup>®</sup>) evaluated by global coagulation assay in patients with acquired haemophilia A.
- Published in:
- Haemophilia, 2024, v. 30, n. 1, p. 249, doi. 10.1111/hae.14902
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- Publication type:
- Article
Longitudinal dynamic changes in factor VIII inhibitor titers in patients with hemophilia A and inhibitors receiving emicizumab prophylaxis.
- Published in:
- International Journal of Hematology, 2023, v. 118, n. 6, p. 690, doi. 10.1007/s12185-023-03667-y
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- Publication type:
- Article
Coagulant potentials of emicizumab in the plasmas from infant and toddler patients with hemophilia A.
- Published in:
- Pediatric Blood & Cancer, 2023, v. 70, n. 10, p. 1, doi. 10.1002/pbc.30590
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- Publication type:
- Article
Intra‐articular haemorrhage caused by reduced recovery of PEGylated recombinant factor VIII due to an anti‐PEG antibody developed after mRNA‐1273 SARS‐CoV‐2 vaccination in haemophilia A.
- Published in:
- Haemophilia, 2023, v. 29, n. 3, p. 935, doi. 10.1111/hae.14786
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- Publication type:
- Article
High levels of factor VIII activity in patients with acquired hemophilia A in remission are associated with unusually low coagulation potentials.
- Published in:
- International Journal of Hematology, 2023, v. 117, n. 5, p. 669, doi. 10.1007/s12185-022-03528-0
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- Publication type:
- Article
Two pediatric cases of severe hemophilia A in which emicizumab prophylaxis failed to prevent traumatic extra-articular hemorrhage.
- Published in:
- International Journal of Hematology, 2023, v. 117, n. 4, p. 607, doi. 10.1007/s12185-022-03490-x
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- Publication type:
- Article
Late‐onset and congenital hearing loss detected using AABR due to congenital cytomegalovirus infection that improved with valganciclovir.
- Published in:
- Congenital Anomalies, 2023, v. 63, n. 2, p. 40, doi. 10.1111/cga.12501
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- Article
First case report of hematidrosis complicated with type 1 von Willebrand disease.
- Published in:
- 2023
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- Publication type:
- Case Study
Activated partial thromboplastin time-based clot waveform analysis enables measurement of very low levels of factor IX activity in patients with severe hemophilia B.
- Published in:
- 2022
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- Publication type:
- journal article
Screening of the protein C pathway abnormality‐related thrombophilia by using thrombomodulin‐mediated tissue factor‐triggered clot waveform analysis.
- Published in:
- European Journal of Haematology, 2022, v. 109, n. 1, p. 100, doi. 10.1111/ejh.13777
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- Publication type:
- Article
Heterogeneous coagulant potential of emicizumab in neonatal factor VIII–deficient plasma.
- Published in:
- Pediatric Blood & Cancer, 2022, v. 69, n. 7, p. 1, doi. 10.1002/pbc.29731
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- Publication type:
- Article
The balance of comprehensive coagulation and fibrinolytic potential is disrupted in patients with moderate to severe COVID-19.
- Published in:
- International Journal of Hematology, 2022, v. 115, n. 6, p. 826, doi. 10.1007/s12185-022-03308-w
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- Publication type:
- Article
Use of thromboelastography before the administration of hemostatic agents to safely taper recombinant activated factor VII in acquired hemophilia A: a report of three cases.
- Published in:
- Thrombosis Journal, 2022, v. 20, n. 1, p. 1, doi. 10.1186/s12959-022-00387-x
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- Publication type:
- Article
A survey of healthcare workers' recommendations about human papillomavirus vaccination.
- Published in:
- Clinical & Experimental Vaccine Research, 2022, v. 11, n. 2, p. 149, doi. 10.7774/cevr.2022.11.2.149
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- Publication type:
- Article
Comparisons of global coagulation potential and bleeding episodes in emicizumab-treated hemophilia A patients and mild hemophilia A patients.
- Published in:
- International Journal of Hematology, 2022, v. 115, n. 4, p. 489, doi. 10.1007/s12185-021-03276-7
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- Publication type:
- Article
Comprehensive blood coagulation potential in patients with acquired hemophilia A: retrospective analyses of plasma samples obtained from nationwide centers across Japan.
- Published in:
- International Journal of Hematology, 2022, v. 115, n. 2, p. 163, doi. 10.1007/s12185-021-03249-w
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- Publication type:
- Article
Plasma-derived factors VIIa and X mixtures (Byclot<sup>®</sup>) significantly improve impairment of coagulant potential ex vivo in plasmas from acquired hemophilia A patients.
- Published in:
- 2020
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- Publication type:
- journal article
Evaluation of clinical severity in patients with type 2N von Willebrand disease using microchip-based flow-chamber system.
- Published in:
- 2020
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- Publication type:
- journal article
Global coagulation function assessed by rotational thromboelastometry predicts coagulation-steady state in individual hemophilia A patients receiving emicizumab prophylaxis.
- Published in:
- 2019
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- Publication type:
- journal article
A case of moderate haemophilia A with inhibitor, carrying the p.R1800H mutation, complicated with juvenile idiopathic arthritis.
- Published in:
- 2019
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- Publication type:
- Case Study
Continuous infusions of B domain-truncated recombinant factor VIII, turoctocog alfa, for orthopedic surgery in severe hemophilia A: first case report.
- Published in:
- 2018
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- Publication type:
- journal article
Factor (F)VIII/VIIa enhances global haemostatic function in the co-presence of bypassing agents and FVIII among patients with haemophilia A with inhibitor.
- Published in:
- British Journal of Haematology, 2018, v. 181, n. 4, p. 528, doi. 10.1111/bjh.15209
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- Publication type:
- Article
First report of real-time monitoring of coagulation function potential and IgG subtype of anti-FVIII autoantibodies in a child with acquired hemophilia A associated with streptococcal infection and amoxicillin.
- Published in:
- 2018
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- Publication type:
- journal article
Efficacy of inchinkoto for a patient with liver fibrosis complicated with transient abnormal myelopoiesis in Down's syndrome.
- Published in:
- Pediatrics International, 2011, v. 53, n. 6, p. 1093, doi. 10.1111/j.1442-200X.2011.03365.x
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- Publication type:
- Article
Type D congenital esophageal atresia associated with omphalomesenteric duct remnant.
- Published in:
- 2010
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- Publication type:
- Letter
Von Willebrand factor protects the Ca<sup>2+</sup>-dependent structure of the factor VIII light chain.
- Published in:
- British Journal of Haematology, 2009, v. 146, n. 5, p. 531, doi. 10.1111/j.1365-2141.2009.07792.x
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- Publication type:
- Article
Protein S down-regulates factor Xase activity independent of activated protein C: specific binding of factor VIII(a) to protein S inhibits interactions with factor IXa.
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- British Journal of Haematology, 2008, v. 143, n. 3, p. 409, doi. 10.1111/j.1365-2141.2008.07366.x
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- Publication type:
- Article
Selective factor VIII and V inactivation by iminodiacetate ion exchange resin through metal ion adsorption.
- Published in:
- British Journal of Haematology, 2008, v. 142, n. 6, p. 962, doi. 10.1111/j.1365-2141.2008.07289.x
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- Publication type:
- Article
Identification of a thrombin-interactive site within the FVIII A2 domain that is responsible for the cleavage at Arg<sup>372</sup>.
- Published in:
- British Journal of Haematology, 2008, v. 140, n. 4, p. 433, doi. 10.1111/j.1365-2141.2007.06935.x
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- Publication type:
- Article
Factor VIII-mediated global hemostasis in the absence of von Willebrand factor.
- Published in:
- 2007
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- Publication type:
- journal article
Relationship between the binding sites for von Willebrand factor, phospholipid, and human factor VIII C2 inhibitor alloantibodies within the factor VIII C2 domain.
- Published in:
- 2007
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- Publication type:
- journal article