Molekulargenetisches Labor
Zentrum für Nephrologie und Stoffwechsel
Erbliche Erkrankungen mit einer erhöhten Blutungsneigung, die auf Störungen der Gerinnungsfaktoren zurückzuführen sind, wurden in dieser Gruppe zusammengefasst.
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Santagostino E et al. (2000) Guidelines on replacement therapy for haemophilia and inherited coagulation disorders in Italy.
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None (2000) Coagulation and bleeding disorders: review and update.
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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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None (1996) Disorders of platelet function.
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