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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: von felten a. Thromb Haemost. 2001 Mar;85(3):454-7. Thromb Haemost. 2001. PMID: 11307814
[The antiphospholipid syndrome: fact or fancy?].
Beer JH, von Felten A. Beer JH, et al. Among authors: von felten a. Schweiz Med Wochenschr. 1993 Nov 20;123(46):2173-4. Schweiz Med Wochenschr. 1993. PMID: 8272786 German. No abstract available.
101 results