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
Citation: U. Wollina et al., Disabling morphoea of childhood - beneficial effect of intravenous immunoglobulin therapy, CLIN EXP D, 23(6), 1998, pp. 292-293