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Citation: A. Decampo et al., A novel splice-site mutation in intron 7 causes more severe hypercholesterolemia than a combined FH-FDB defect, ATHEROSCLER, 157(2), 2001, pp. 524-525

Authors: Renner, W Koppel, H Brodmann, M Pabst, E Schallmoser, K Toplak, H Wascher, TC Pilger, E

Citation: W. Renner et al., Factor II G20210A and factor V G1691A gene mutations and peripheral arterial occlusive disease, THROMB HAEM, 83(1), 2000, pp. 20-22

Authors: Renner, W Koppel, H Hoffmann, C Schallmoser, K Stanger, O Toplak, H Wascher, TC Pilger, E

Citation: W. Renner et al., Prothrombin G20210A, factor V Leiden, and factor XIII Va134Leu: Common mutations of blood coagulation factors and deep vein thrombosis in Austria, THROMB RES, 99(1), 2000, pp. 35-39

Authors: Renner, W Schallmoser, K Gallippi, P Krauss, C Toplak, H Wascher, TC Pilger, E

Citation: W. Renner et al., C242T polymorphism of the p22 phox gene is not associated with peripheral arterial occlusive disease, ATHEROSCLER, 152(1), 2000, pp. 175-179

Authors: de Campo, A Toplak, H Wascher, TC Schallmoser, K Friehs, A Schmidt, H Kostner, GM

Citation: A. De Campo et al., Evaluation of a newly discovered LDL-receptor-mutation (exon 10, GAC > AAC, D471N, "FH graz-1") in familial hypercholesterolemia - a family study, ACT MED AUS, 26(1), 1999, pp. 20-25