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jbc.org
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Sodetz JM, Paulson JC, McKee PA. Carbohydrate composition and identification of blood group A, B, and H oligosaccharide structures on human factor VIII/von Willebrand factor. J Biol Chem. 1979, roč. 254, čís. 21, s. 10754–10760. Dostupné online. PMID315409.
Zheng X, Chung D, Takayama TK, Majerus EM, Sadler JE, Fujikawa K. Structure of von Willebrand factor-cleaving protease (ADAMTS13), a metalloprotease involved in thrombotic thrombocytopenic purpura.. J Biol Chem.. 2001, roč. 276, s. 41059–41063. [http:// Dostupné online]. doi:10.1074/jbc.C100515200. PMID11557746.
Levy GG, Nichols WC, Lian EC, Foroud T, McClintick JN, McGee BM, Yang AY, Siemieniak DR, Stark KR, Gruppo R, Sarode R, Shurin SB, Chandrasekaran V, Stabler SP, Sabio H, Bouhassira EE, Upshaw JD Jr, Ginsburg D, Tsai HM. Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura.. Nature. 2001, roč. 413, s. 488–494. [http:// Dostupné online]. doi:10.1038/35097008. PMID11586351.
Sadler JE, Budde U, Eikenboom JC, et al.. Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor. J. Thromb. Haemost.. 2006, roč. 4, čís. 10, s. 2103–14. Dostupné online. doi:10.1111/j.1538-7836.2006.02146.x. PMID16889557.
Vincentelli A, Susen S, Le Tourneau T, et al.. Acquired von Willebrand syndrome in aortic stenosis. N. Engl. J. Med.. 2003, roč. 349, čís. 4, s. 343–9. Dostupné v archivu pořízeném dne 2010-02-21. doi:10.1056/NEJMoa022831. PMID12878741.
Vincentelli A, Susen S, Le Tourneau T, et al.. Acquired von Willebrand syndrome in aortic stenosis. N. Engl. J. Med.. 2003, roč. 349, čís. 4, s. 343–9. Dostupné v archivu pořízeném dne 2010-02-21. doi:10.1056/NEJMoa022831. PMID12878741.
worldcat.org
PARETI, F I. Isolation and characterization of a collagen binding domain in human von Willebrand factor. J. Biol. Chem.. Nov. 1986, roč. 261, čís. 32, s. 15310-5. ISSN0021-9258. PMID3490481.