Seminars in Thrombosis and Hemostasis
Ausgabe 04 · Juni 2016
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Editorial
325
Favaloro, Emmanuel J.:
2016 Eberhard F. Mammen Award Announcements: Part I — Most Popular Articles
FREIER ZUGRIFF
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Preface
331
Lisman, Ton; de Moerloose, Philippe:
The Role of Fibrinogen and Factor XIII in Hemostasis, and the Identification and Treatment of Associated Disorders
FREIER ZUGRIFF
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333
Litvinov, Rustem I.; Weisel, John W.:
What Is the Biological and Clinical Relevance of Fibrin?
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344
Macrae, Fraser L.; Domingues, Marco M.; Casini, Alessandro; Ariëns, Robert A. S.:
The (Patho)physiology of Fibrinogen γ′
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356
Neerman-Arbez, Marguerite; de Moerloose, Philippe; Casini, Alessandro:
Laboratory and Genetic Investigation of Mutations Accounting for Congenital Fibrinogen Disorders
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366
Casini, Alessandro; de Moerloose, Philippe; Neerman-Arbez, Marguerite:
Clinical Features and Management of Congenital Fibrinogen Deficiencies
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PDF (182 kb)
375
Samama, Charles Marc:
Fibrinogen Concentrates for Acquired Fibrinogen Deficiencies?
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PDF (111 kb)
381
Undas, Anetta:
How to Assess Fibrinogen Levels and Fibrin Clot Properties in Clinical Practice?
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PDF (230 kb)
389
Lisman, Ton; Ariëns, Robert A. S.:
Alterations in Fibrin Structure in Patients with Liver Diseases
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PDF (129 kb)
397
Kopec, Anna K.; Luyendyk, James P.:
Role of Fibrin(ogen) in Progression of Liver Disease: Guilt by Association?
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408
Ko, Ya-Ping; Flick, Matthew J.:
Fibrinogen Is at the Interface of Host Defense and Pathogen Virulence in
Staphylococcus aureus
Infection
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PDF (325 kb)
422
Schroeder, Verena; Kohler, Hans P.:
Factor XIII: Structure and Function
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PDF (297 kb)
429
Muszbek, László; Katona, Éva:
Diagnosis and Management of Congenital and Acquired FXIII Deficiencies
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PDF (246 kb)
440
Lassila, Riitta:
Clinical Use of Factor XIII Concentrates
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445
Byrnes, James R.; Wolberg, Alisa S.:
Newly-Recognized Roles of Factor XIII in Thrombosis
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Letter to the Editor
455
Simurda, Tomas; Snahnicanova, Zuzana; Loderer, Dusan; Sokol, Juraj; Stasko, Jan; Lasabova, Zora; Kubisz, Peter:
Fibrinogen Martin: A Novel Mutation in
FGB
(Gln180Stop) Causing Congenital Afibrinogenemia
FREIER ZUGRIFF
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