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Genetic predisposition to bleeding during oral anticoagulant therapy: evidence for common founder mutations (FIXVal-10 and FIXThr-10) and an independent CpG hotspot mutation (FIXThr-10).
Oldenburg J, Kriz K, Wuillemin WA, Maly FE, von Felten A, Siegemund A, Keeling DM, Baker P, Chu K, Konkle BA, Lämmle B, Albert T; Study Group on Hereditary Warfarin Sensitivity. Oldenburg J, et al. Among authors: baker p. Thromb Haemost. 2001 Mar;85(3):454-7. Thromb Haemost. 2001. PMID: 11307814
Guideline for laboratory diagnosis and monitoring of von Willebrand disease: A joint guideline from the United Kingdom Haemophilia Centre Doctors' Organisation and the British Society for Haematology.
Platton S, Baker P, Bowyer A, Keenan C, Lawrence C, Lester W, Riddell A, Sutherland M. Platton S, et al. Among authors: baker p. Br J Haematol. 2024 May;204(5):1714-1731. doi: 10.1111/bjh.19385. Epub 2024 Mar 26. Br J Haematol. 2024. PMID: 38532595 No abstract available.
2,912 results