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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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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None (2000) Coagulation and bleeding disorders: review and update. [^] |
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None (2001) Vascular thrombohemorrhagic disorders: hereditary and acquired. [^] |
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None (2004) Inherited bleeding disorders: disorders of platelet adhesion and aggregation. [^] |
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None (2005) von Willebrand disease in the developing world. [^] |
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Peyvandi F et al. (2006) Genetic diagnosis of haemophilia and other inherited bleeding disorders. [^] |
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Asselta R et al. (2006) The molecular basis of quantitative fibrinogen disorders. [^] |
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Dargaud Y et al. (2007) Haemophilia therapies. [^] |
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Franchini M et al. (2007) Prophylaxis in von Willebrand disease. [^] |
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Hill M et al. (2008) Diagnosis, clinical features and molecular assessment of the dysfibrinogenaemias. [^] |
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None (2009) Role of antithrombin concentrate in treatment of hereditary antithrombin deficiency. An update. [^] |
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