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The prevalence of the cysteine1584 variant of von Willebrand factor is increased in type 1 von Willebrand disease: co-segregation with increased susceptibility to ADAMTS13 proteolysis but not clinical phenotype.
Bowen DJ, Collins PW, Lester W, Cumming AM, Keeney S, Grundy P, Enayat SM, Bolton-Maggs PH, Keeling DM, Khair K, Tait RC, Wilde JT, Pasi KJ, Hill FG; UK Haemophilia Centre Doctors' Organization. Bowen DJ, et al. Among authors: keeling dm. Br J Haematol. 2005 Mar;128(6):830-6. doi: 10.1111/j.1365-2141.2005.05375.x. Br J Haematol. 2005. PMID: 15755288 Free article.
The diagnosis and management of von Willebrand disease: a United Kingdom Haemophilia Centre Doctors Organization guideline approved by the British Committee for Standards in Haematology.
Laffan MA, Lester W, O'Donnell JS, Will A, Tait RC, Goodeve A, Millar CM, Keeling DM. Laffan MA, et al. Among authors: keeling dm. Br J Haematol. 2014 Nov;167(4):453-65. doi: 10.1111/bjh.13064. Epub 2014 Aug 12. Br J Haematol. 2014. PMID: 25113304 Free PMC article. Review. No abstract available.
Changing patterns of bleeding in patients with severe haemophilia A.
Stephensen D, Tait RC, Brodie N, Collins P, Cheal R, Keeling D, Melton K, Dolan G, Haye H, Hayman E, Winter M. Stephensen D, et al. Haemophilia. 2009 Nov;15(6):1210-4. doi: 10.1111/j.1365-2516.2008.01876.x. Epub 2009 Jul 29. Haemophilia. 2009. PMID: 19659938
Perioperative replacement therapy in haemophilia B: An appeal to "B" more precise.
Hazendonk HCAM, Preijers T, Liesner R, Chowdary P, Hart D, Keeling D, Driessens MHE, Laros-van Gorkom BAP, van der Meer FJM, Meijer K, Fijnvandraat K, Leebeek FWG, Mathôt RAA, Collins PW, Cnossen MH. Hazendonk HCAM, et al. Haemophilia. 2018 Jul;24(4):611-618. doi: 10.1111/hae.13469. Epub 2018 Apr 29. Haemophilia. 2018. PMID: 29707861 Free article.
154 results