Thrombosis and Haemostasis, Table of Contents Thromb Haemost 2007; 98(01): 8-15DOI: 10.1160/TH07-05-0343 Anniversary Issue Contribution Schattauer GmbH Thrombosis and haemostasis research: Stimulating, hard work and fun Margareta Blombäck 1 Department of Molecular Medicine and Surgery, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden › Author AffiliationsRecommend Article Abstract Full Text References References 1 Mutt V, Blombäck M. Erik Jorpes-a pragmatic physiological clinical chemist. Selected topics in the History of Biochemistry: Personal Recollections VI. Compr Biochem 2000; 41: 363-389. 2 Blombäck B, Blombäck M. Purification of human and bovine fibrinogen. Arkiv Kemi 1956; 10: 415-443. 3 Blombäck B. Travels with fibrinogen. J Thromb Haemost 2006; 4: 1653-1660. 4 Blombäck B. Chapter 6: Journey with bleeding time factor. In: Stories of success. Personal Recollections. Compr Biochem. Vol. 45 211-258 Elsevier Science BV; 2008 5 Blombäck B. 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Structure-function relationship of factor VIII complex studied by thioredoxin dependent disulfide reduction. Thromb Res 1984; 35: 637-651. 30 Thorell L, Blombäck M, Blombäck B. An in vivo study of a new factor VIII high purity preparation. Thromb Res 1983; 31: 375-385. 31 Heimburger N. Advances in hemophilia treatment: a hepatitis-safe factor VIII concentrate. Blut 1982; 44: 249-251. 32 Anvret M, Blombäck M, Lindstedt M. et al. Genetic and coagulation characterization of Swedish families with von Willebrand’s disease types I and III: New aspects of heredity. Human Genetics 1992; 89: 147-154. 33 Zhang ZP, Falk G, Blombäck M. et al. A single cytosine deletion in exon 18 of the von Willebrand factor geneis the most common mutation in Swedish vWD type III patients. Hum Mol Genet 1992; 1: 767-768. 34 Zhang ZP, Lindstedt M, Falk G. et al. Nonsense mutations of the von Willebrand factor gene in patients with von Willebrand’s disease type III and I. 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