Erbliche Blutungsübel
Erbliche Erkrankungen mit einer erhöhten Blutungsneigung, die auf Störungen der Gerinnungsfaktoren zurückzuführen sind, wurden in dieser Gruppe zusammengefasst.
Gliederung
Referenzen:
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Basi DL et al. (1999) Bleeding and coagulation problems in the dental patient. Hereditary disease and medication-induced risks. [^] |
| 2. |
Baker WF et al. (1999) Treatment of hereditary and acquired thrombophilic disorders. [^] |
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Nitu-Whalley IC et al. (1999) Acquired von Willebrand syndrome--report of 10 cases and review of the literature. [^] |
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| 5. |
Triplett DA et al. (2000) Coagulation and bleeding disorders: review and update. [^] |
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Bick R et al. (2001) Vascular thrombohemorrhagic disorders: hereditary and acquired. [^] |
| 7. |
Ramasamy I et al. (2004) Inherited bleeding disorders: disorders of platelet adhesion and aggregation. [^] |
| 8. |
Roberts HR et al. (2004) Current concepts of hemostasis: implications for therapy. [^] |
| 9. |
Srivastava A et al. (2005) von Willebrand disease in the developing world. [^] |
| 10. |
Peyvandi F et al. (2006) Genetic diagnosis of haemophilia and other inherited bleeding disorders. [^] |
| 11. |
Asselta R et al. (2006) The molecular basis of quantitative fibrinogen disorders. [^] |
| 12. |
Dargaud Y et al. (2007) Haemophilia therapies. [^] |
| 13. |
Franchini M et al. (2007) Prophylaxis in von Willebrand disease. [^] |
| 14. |
Hill M et al. (2008) Diagnosis, clinical features and molecular assessment of the dysfibrinogenaemias. [^] |
| 15. |
Rodgers GM et al. (2009) Role of antithrombin concentrate in treatment of hereditary antithrombin deficiency. An update. [^] |
| 16. |
Fuse I et al. (1996) Disorders of platelet function. [^] |
