DOI: 10.1055/s-00000077

Seminars in Thrombosis and Hemostasis

Ausgabe 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

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Favaloro, Emmanuel J.: 2013 Eberhard F. Mammen Award Announcements

Preface

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

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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