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Treatment of factor VIII inhibitors.

作者信息

Kasper C K

出版信息

Prog Hemost Thromb. 1989;9:57-86.

PMID:2492380
Abstract
摘要

相似文献

1
Treatment of factor VIII inhibitors.
Prog Hemost Thromb. 1989;9:57-86.
2
Acquired hemophilia.获得性血友病
Haematologica. 1994 Nov-Dec;79(6):550-6.
3
Acquired inhibitors.获得性抑制剂
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4
[Successful treatment of massive hemorrhagic diathesis caused by Factor VIII:C-antibodies with adsorption plasmapheresis and immunosuppression].[采用吸附性血浆置换和免疫抑制疗法成功治疗由VIII因子：C抗体引起的大量出血素质]
Med Klin (Munich). 1991 Mar 15;86(3):165-70, 171.
5
Acquired hemophilia and its treatment.
Blood Coagul Fibrinolysis. 1997 Aug;8 Suppl 1:S15-8.
6
[Combined treatment with factor VIII and immunosuppressive agents in a young woman with acquired factor VIII inhibitor].[一名获得性因子 VIII 抑制剂年轻女性患者采用因子 VIII 与免疫抑制剂联合治疗]
Sangre (Barc). 1996 Apr;41(2):147-50.
7
Factor VIII inhibitors.凝血因子VIII抑制剂
Adv Exp Med Biol. 2001;489:65-73. doi: 10.1007/978-1-4615-1277-6_6.
8
[Factor VIII inhibitors--their characteristics and clinical significance].[凝血因子 VIII 抑制剂——其特性及临床意义]
Pol Arch Med Wewn. 1987 Dec;78(6):333-40.
9
Inhibitors to factor VIII in a family with mild hemophilia: molecular characterization and response to factor VIII and desmopressin.
Thromb Haemost. 1995 Aug;74(2):619-21.
10
[Acquired factor VIII inhibitor in a patient with rheumatoid arthritis].[一名类风湿关节炎患者获得性凝血因子VIII抑制剂]
Sangre (Barc). 1993 Oct;38(5):403-5.

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Management of Odontogenic Fascial Space Infection in Hemophilia Patients: A Proposed Protocol.血友病患者牙源性筋膜间隙感染的管理：一项拟议方案。
J Maxillofac Oral Surg. 2019 Jun;18(2):197-202. doi: 10.1007/s12663-018-1117-0. Epub 2018 May 9.
2
"Antihemophilic factor is not the only answer for all factor VIII deficiencies." Case report of odontogenic infection in a patient with hemophilia A, complicated by factor VIII inhibitors, and managed by transfusion of antihemophilic factor and factor VIII inhibitor bypass activity.抗血友病因子并非所有VIII因子缺乏症的唯一解决方案。一名甲型血友病患者发生牙源性感染的病例报告，该患者并发VIII因子抑制剂，并通过输注抗血友病因子和VIII因子抑制剂旁路活性进行治疗。
Indian J Dent. 2016 Sep;7(3):149-152. doi: 10.4103/0975-962X.186700.
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Acquired inhibitors of clotting factors: AICE recommendations for diagnosis and management.获得性凝血因子抑制剂：AICE关于诊断和管理的建议
Blood Transfus. 2015 Jul;13(3):498-513. doi: 10.2450/2015.0141-15. Epub 2015 Jun 24.
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Pharmacokinetics of coagulation factors: clinical relevance for patients with haemophilia.凝血因子的药代动力学：对血友病患者的临床意义
Clin Pharmacokinet. 2001;40(11):815-32. doi: 10.2165/00003088-200140110-00003.
5
Genetic induction of immune tolerance to human clotting factor VIII in a mouse model for hemophilia A.在甲型血友病小鼠模型中对人凝血因子 VIII 的免疫耐受的基因诱导。
Proc Natl Acad Sci U S A. 1998 May 12;95(10):5734-9. doi: 10.1073/pnas.95.10.5734.
6
Haemophilia.血友病
Postgrad Med J. 1997 Apr;73(858):201-6. doi: 10.1136/pgmj.73.858.201.
7
Acquired factor VIII inhibitor preceding chronic lymphocytic leukemia.
Ann Hematol. 1993 Dec;67(6):309-11. doi: 10.1007/BF01696353.
8
Hemophilia and von Willebrand's disease: 1. Diagnosis, comprehensive care and assessment. Association of Hemophilia Clinic Directors of Canada.血友病和血管性血友病：1. 诊断、综合护理与评估。加拿大血友病诊所主任协会。
CMAJ. 1995 Jul 1;153(1):19-25.
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Congenital bleeding disorders. Rational treatment options.
Drugs. 1993 Apr;45(4):541-7. doi: 10.2165/00003495-199345040-00006.