Results: 1-6 |
Results: 6

Authors: Poon, MC d'Oiron, R Hann, I Negrier, C de Lumley, L Thomas, A Karafoulidou, A Demers, C Street, A Huth-Kuhne, A Petrini, P Fressinaud, E Morfini, M Tengborn, L Marques-Verdier, A Musso, R Devecioglu, O Houston, DS Lethagen, S Van Geet, C von Depka, M Berger, C Beurrier, P Britton, HA Gerrits, W Guthner, C Kuhle, S Lorenzo, JJ Makris, PE Nohe, N Paugy, P Pautard, B Torchet, MF Trillot, N Vicariot, M Wilde, J Winter, M Chambost, H Ingerslev, J Peters, M Strauss, G
Citation: Mc. Poon et al., Use of recombinant factor VIIa (NovoSeven (R)) in patients with Glanzmann thrombasthenia, SEM HEMATOL, 38(4), 2001, pp. 21-25

Authors: Subtil, D Deruelle, P Trillot, N Jude, B
Citation: D. Subtil et al., Preclinical phase of polycythemia vera in pregnancy, OBSTET GYN, 98(5), 2001, pp. 945-947

Authors: Hachulla, E Rose, C Trillot, N Caulier-Leleu, MT Pasturel-Michon, U
Citation: E. Hachulla et al., What vascular events suggest a myeloproliferative disorder?, J MAL VASC, 25(5), 2000, pp. 382-387

Authors: Trillot, N Zawadzki, C Watel, A Jude, B
Citation: N. Trillot et al., The G20210A transition in the prothrombin gene and venous thromboembolic disease., REV MED IN, 21(10), 2000, pp. 911-914

Authors: Trillot, N Rugeri, L Jude, B
Citation: N. Trillot et al., Inherited thrombophilia: laboratory evaluation and therapeutic implications, THERAPIE, 54(4), 1999, pp. 413-418

Authors: Zawadzki, C Gaveriaux, V Trillot, N Bauters, A Watel, A Alhenc-Gelas, M Preudhomme, C Jude, B
Citation: C. Zawadzki et al., Homozygous G20210A transition in the prothrombin gene associated with severe venous thrombotic disease: Two cases in a French family, THROMB HAEM, 80(6), 1998, pp. 1027-1028
Risultati: 1-6 |