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Authors: Herrmann, FH Wulff, K Auberger, K Aumann, V Bergmann, F Bergmann, K Bratanoff, E Franke, D Grundeis, M Kreuz, W Lenk, H Losonczy, H Maak, B Marx, G Mauz-Korholz, C Pollmann, H Serban, M Sutor, A Syrbe, G Vogel, G Weinstock, N Wenzel, E Wolf, K
Citation: Fh. Herrmann et al., Molecular biology and clinical manifestation of hereditary factor VII deficiency, SEM THROMB, 26(4), 2000, pp. 393-400

Authors: Maak, B Wulff, K Herrmann, FH Schroder, W Budde, U Siegemund, A Ruhling, H
Citation: B. Maak et al., Factor XII deficiency, APC-resistance, hyperhomocysteinemia and von Willebrand's disease type 1 in the same family, MONATS KIND, 147(2), 1999, pp. 104-109

Authors: Wollina, U Looks, A Schneider, R Maak, B
Citation: U. Wollina et al., Disabling morphoea of childhood - beneficial effect of intravenous immunoglobulin therapy, CLIN EXP D, 23(6), 1998, pp. 292-293
Risultati: 1-3 |