Seminars in Thrombosis and Hemostasis
Ausgabe 02 · März 2006
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PREFACE
079
Mammen, Eberhard F.:
Thrombotic Microangiopathies
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081
Biol, Miriam Galbusera; Noris, Marina; Remuzzi, Giuseppe:
Thrombotic Thrombocytopenic Purpura-Then and Now
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090
Loirat, Chantal; Veyradier, Agnès; Girma, Jean-Pierre; Ribba, Anne-Sophie; Meyer, Dominique:
Thrombotic Thrombocytopenic Purpura Associated with von Willebrand Factor-Cleaving Protease (ADAMTS13) Deficiency in Children
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098
Kentouche, Karim; Zintl, Felix; Angerhaus, Dorothea; Fuchs, Dietlinde; Hermann, Johann; Schneppenheim, Reinhard; Budde, Ulrich:
von Willebrand Factor-Cleaving Protease (ADAMTS13) in the Course of Stem Cell Transplantation
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105
Karch, Helge; Friedrich, Alexander W.; Gerber, Angela; Zimmerhackl, Lothar B.; Schmidt, M. Alexander; Bielaszewska, Martina:
New Aspects in the Pathogenesis of Enteropathic Hemolytic Uremic Syndrome
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113
Zimmerhackl, L. Bernd; Besbas, Nesir; Jungraithmayr, Therese; Kar, Nicole van de; Karch, Helge; Karpman, Diana; Landau, Daniel; Loirat, Chantal; Proesmans, Willem; Prüfer, Friederike; Rizzoni, Gianfranco; Taylor, Mark C.; for the European Study Group for Haemolytic Uraemic Syndromes and Related Disorders:
Epidemiology, Clinical Presentation, and Pathophysiology of Atypical and Recurrent Hemolytic Uremic Syndrome
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121
Prüfer, Friederike; Scheiring, Johanna; Sautter, Sabine; Jensen, Dorthe B.; Treichl, Ruth; Würzner, Reinhard; Zimmerhackl, L. Bernd:
Terminal Complement Complex (C5b-9) in Children with Recurrent Hemolytic Uremic Syndrome
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128
Karpman, Diana; Manea, Minola; Vaziri-Sani, Fariba; Ståhl, Anne-lie; Kristoffersson, Ann-Charlotte:
Platelet Activation in Hemolytic Uremic Syndrome
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146
Licht, Christoph; Skerka, Christine; Misselwitz, Joachim; Zipfel, Peter F.:
The Role of Defective Complement Control in Hemolytic Uremic Syndrome
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155
Kavanagh, David; Goodship, Timothy H. J.:
Membrane Cofactor Protein and Factor I: Mutations and Transplantation
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160
Saunders, Rebecca E.; Perkins, Stephen J.:
A User's Guide to the Interactive Web Database of Factor H-Associated Hemolytic Uremic Syndrome
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