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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: khair k. 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.
Stem cell transplantation for children with Glanzmann thrombasthenia.
Connor P, Khair K, Liesner R, Amrolia P, Veys P, Ancliff P, Mathias M. Connor P, et al. Among authors: khair k. Br J Haematol. 2008 Mar;140(5):568-71. doi: 10.1111/j.1365-2141.2007.06890.x. Epub 2008 Jan 16. Br J Haematol. 2008. PMID: 18205861 Free article.
Purpura fulminans: recognition, diagnosis and management.
Chalmers E, Cooper P, Forman K, Grimley C, Khair K, Minford A, Morgan M, Mumford AD. Chalmers E, et al. Among authors: khair k. Arch Dis Child. 2011 Nov;96(11):1066-71. doi: 10.1136/adc.2010.199919. Epub 2011 Jan 12. Arch Dis Child. 2011. PMID: 21233082 Review.
128 results