DOI: 10.1055/s-00000077

Seminars in Thrombosis and Hemostasis

Issue 06 · Volume 39 · September 2013 DOI: 10.1055/s-003-25548 Rare Bleeding Disorders: Genetic, Laboratory, Clinical, and Molecular Aspects Guest Editor, Maha Othman, MD, PhD

Editorial

  • 567
    Favaloro, Emmanuel J.:

    2013 Eberhard F. Mammen Award Announcements

    • Preface

  • 575
    Othman, Maha:

    Rare Bleeding Disorders: Genetic, Laboratory, Clinical, and Molecular Aspects

  • 579
    Peyvandi, Flora; Menegatti, Marzia; Palla, Roberta:

    Rare Bleeding Disorders: Worldwide Efforts for Classification, Diagnosis, and Management

  • 585
    de Moerloose, Philippe; Casini, Alessandro; Neerman-Arbez, Marguerite:

    Congenital Fibrinogen Disorders: An Update

  • 596
    Lancellotti, Stefano; Basso, Maria; De Cristofaro, Raimondo:

    Congenital Prothrombin Deficiency: An Update

  • 607
    Thalji, Nabil; Camire, Rodney M.:

    Parahemophilia: New Insights into Factor V Deficiency

  • 613
    Zheng, Chunlei; Zhang, Bin:

    Combined Deficiency of Coagulation Factors V and VIII: An Update

  • 621
    Duga, Stefano; Salomon, Ophira:

    Congenital Factor XI Deficiency: An Update

  • 632
    Schroeder, Verena; Kohler, Hans P.:

    Factor XIII Deficiency: An Update

  • 642
    Nurden, Alan T.; Pillois, Xavier; Wilcox, David A.:

    Glanzmann Thrombasthenia: State of the Art and Future Directions

  • 656
    Andrews, Robert K.; Berndt, Michael C.:

    Bernard–Soulier Syndrome: An Update

  • 663
    Othman, Maha; Kaur, Harmanpreet; Emsley, Jonas:

    Platelet-Type von Willebrand Disease: New Insights into the Molecular Pathophysiology of a Unique Platelet Defect

  • 674
    Kubisz, Peter; Stasko, Jan; Holly, Pavol:

    Sticky Platelet Syndrome

  • 684
    Ruiz-Saez, Arlette:

    Occurrence of Thrombosis in Rare Bleeding Disorders