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Literature DB >> 9277004

Inherited thrombophilia: memorandum from a joint WHO/International Society on Thrombosis and Haemostasis meeting.

Abstract

Inherited thrombophilias are common disorders with a worldwide distribution, including antithrombin, protein C, and protein S deficiencies as well as resistance to activated protein C. Increased understanding of these disorders suggests that thrombophilia can arise from interaction between defective genes and environmental factors. WHO and the international Society on Thrombosis and Haemostasis (ISTH) discussed the problems of inherited thrombophilia at a joint meeting held in Geneva on 6-8 November 1995. The present article reports on the various possibilities for controlling the disorder and makes a series of recommendations for diagnosis, treatment, and research into the condition.

Entities: Disease Gene

Mesh：

Year: 1997 PMID： 9277004 PMCID： PMC2486958

Source DB: PubMed Journal: Bull World Health Organ ISSN： 0042-9686 Impact factor: 9.408

47 in total

Review 1. Anticoagulants during pregnancy.

Authors: J S Ginsberg; J Hirsh
Journal: Annu Rev Med Date: 1989 Impact factor: 13.739

2. The frequency of type I heterozygous protein S and protein C deficiency in 141 unrelated young patients with venous thrombosis.

Authors: C L Gladson; I Scharrer; V Hach; K H Beck; J H Griffin
Journal: Thromb Haemost Date: 1988-02-25 Impact factor: 5.249

3. Familial elevation of plasma histidine-rich glycoprotein in a family with thrombophilia.

Authors: L Engesser; C Kluft; E Briët; E J Brommer
Journal: Br J Haematol Date: 1987-11 Impact factor: 6.998

Review 4. Different prevalence of thromboembolism in the subtypes of congenital antithrombin III deficiency: review of 404 cases.

Authors: G Finazzi; R Caccia; T Barbui
Journal: Thromb Haemost Date: 1987-12-18 Impact factor: 5.249

5. Isolation and characterization of a human plasma protein with affinity for the lysine binding sites in plasminogen. Role in the regulation of fibrinolysis and identification as histidine-rich glycoprotein.

Authors: H R Lijnen; M Hoylaerts; D Collen
Journal: J Biol Chem Date: 1980-11-10 Impact factor: 5.157

Review 6. Clinical experience with antithrombin III concentrate in treatment of congenital and acquired deficiency of antithrombin. The Antithrombin III Study Group.

Authors: R S Schwartz; K A Bauer; R D Rosenberg; E J Kavanaugh; D C Davies; D A Bogdanoff
Journal: Am J Med Date: 1989-09-11 Impact factor: 4.965

Inherited thrombophilia: memorandum from a joint WHO/International Society on Thrombosis and Haemostasis meeting.

Review 1. Anticoagulants during pregnancy.

2. The frequency of type I heterozygous protein S and protein C deficiency in 141 unrelated young patients with venous thrombosis.

3. Familial elevation of plasma histidine-rich glycoprotein in a family with thrombophilia.

Review 4. Different prevalence of thromboembolism in the subtypes of congenital antithrombin III deficiency: review of 404 cases.

5. Isolation and characterization of a human plasma protein with affinity for the lysine binding sites in plasminogen. Role in the regulation of fibrinolysis and identification as histidine-rich glycoprotein.

Review 6. Clinical experience with antithrombin III concentrate in treatment of congenital and acquired deficiency of antithrombin. The Antithrombin III Study Group.

7. Absence of thrombosis in subjects with heterozygous protein C deficiency.

Review 8. A review of mutations causing deficiencies of antithrombin, protein C and protein S.

9. The relative frequency of hereditary thrombotic disorders among 107 patients with thrombophilia in Israel.

10. Purpura fulminans in a Chinese boy with congenital protein C deficiency.

1. Role of investigating thrombophilic disorders in young stroke.

2. Protein S Deficiency and the Risk of Venous Thromboembolism in the Han Chinese Population.