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Results: 1-8 |
Results: 8

Authors: Vanhoorelbeke, K Schlammadinger, A Delville, JP Handsaeme, J Vandecasteele, G Vauterin, S Pradier, O Wijns, W Deckmyn, H
Citation: K. Vanhoorelbeke et al., Occurrence of the Asn45Ser mutation in the GPIX gene in a Belgian patient with Bernard Soulier syndrome, PLATELETS, 12(2), 2001, pp. 114-120

Authors: Cauwenberghs, N Schlammadinger, A Vauterin, S Cooper, S Descheemaeker, G Tornai, I Deckmyn, H
Citation: N. Cauwenberghs et al., Fc-receptor dependent platelet aggregation induced by monoclonal antibodies against platelet glycoprotein Ib or von Willebrand factor, THROMB HAEM, 85(4), 2001, pp. 679-685

Authors: Rejto, L Schlammadinger, A Laszlo, P Kiss, A Telek, B Boda, Z
Citation: L. Rejto et al., Use of a platelet filter test in patients with thrombocytosis, PLATELETS, 11(1), 2000, pp. 38-42

Authors: Schlammadinger, A Kerenyi, A Muszbek, L Boda, Z
Citation: A. Schlammadinger et al., Comparison at the O'Brien filter test and the PFA-100 platelet analyzer inthe laboratory diagnosis of von Willebrand's disease, THROMB HAEM, 84(1), 2000, pp. 88-92

Authors: Vanhoorelbeke, K Cauwenberghs, N Vauterin, S Schlammadinger, A Mazurier, C Deckmyn, H
Citation: K. Vanhoorelbeke et al., A reliable and reproducible ELISA method to measure ristocetin cofactor activity of von Willebrand factor, THROMB HAEM, 83(1), 2000, pp. 107-113

Authors: Boda, Z Laszlo, P Pfliegler, G Tornai, I Rejto, L Schlammadinger, A
Citation: Z. Boda et al., Low molecular weight heparin as thromboprophylaxis throughout pregnancy inheritable thrombophilic women, CL APPL T-H, 5(3), 1999, pp. 198-199

Authors: Tornai, I Boda, Z Schlammadinger, A Juhasz, A Cauwenberghs, N Deckmyn, H
Citation: I. Tornai et al., Acquired Bernaud-Soulier syndrome: A case with necrotizing vasculitis and thrombosis, HAEMOSTASIS, 29(4), 1999, pp. 229-236

Authors: Kerenyi, A Schlammadinger, A Ajzner, E Szegedi, I Kiss, C Pap, Z Boda, Z Muszbek, L
Citation: A. Kerenyi et al., Comparison of PFA-100 closure time and template bleeding time of patients with inherited disorders causing defective platelet function, THROMB RES, 96(6), 1999, pp. 487-492
Risultati: 1-8 |