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Number of items: 4.

Sandrock-Lang, K; Oldenburg, J; Wiegering, V; Halimeh, S; Santoso, S; Kurnik, K; Fischer, L; Tsakiris, D A; Sigl-Kraetzig, M; Brand, B; Bührlen, M; Kraetzer, K; Deeg, N; Hund, M; Busse, E; Kahle, A; Zieger, B (2015). Characterisation of patients with Glanzmann thrombasthenia and identification of 17 novel mutations. Thrombosis and Haemostasis, 113(4):782-791.

Knöfler, R; Eberl, W; Schulze, H; Bakchoul, T; Bergmann, F; Gehrisch, S; Geisen, C; Gottstein, S; Halimeh, S; Harbrecht, U; Kappert, G; Kirchmaier, C; Kehrel, B; Lösche, W; Krause, M; Mahnel, R; Meyer, O; Pilgrimm, A K; Pillitteri, D; Rott, H; Santoso, S; Siegemund, A; Schambeck, C; Scheer, M; Schmugge, M; Scholl, T; Strauss, G; Zieger, B; Zotz, R; Hermann, M; Streif, W (2014). Diagnose angeborener Störungen der Thrombozytenfunktion Interdisziplinäre S2K-Leitlinie der Ständigen Kommission Pädiatrie der Gesellschaft für Thrombose- und Hämostaseforschung e. V. Hämostaseologie, 34(3):201-212.

Pecci, A; Klersy, C; Gresele, P; Lee, K J; De Rocco, D; Bozzi, V; Russo, G; Heller, P G; Loffredo, G; Ballmeier, M; Fabris, F; Beggiato, E; Kahr, W H; Pujol-Moix, N; Platokouki, H; Van Geet, C; Noris, P; Yerram, P; Hermans, C; Gerber, B; Economou, M; De Groot, M; Zieger, B; De Candia, E; Fraticelli, V; Kersseboom, R; Piccoli, G C; Zimmermann, S; Fierro, T; Glembotsky, A C; Vianello, F; Zaninetti, C; Nicchia, E; Güthner, C; Baronci, C; Seri, M; Knight, P J; Balduini, C I; Savoia, A (2014). MYH9-related disease: a novel prognostic model to predict the clinical evolution of the disease based on genotype-phenotype correlations. Human Mutation, 35(2):236-247.

Streif, W; Knöfler, R; Eberl, W; Andres, O; Bakchoul, T; Bergmann, F; Beutel, K; Dittmer, R; Gehrisch, S; Gottstein, S; Halimeh, S; Haselböck, J; Hassenpflug, W-A; Heine, S; Holzhauer, S; King, S; Kirchmaier, C M; Krause, M; Kreuz, W; Lösche, W; Mahnel, R; Maurer, M; Nimtz-Talaska, A; Olivieri, M; Rott, H; Schambeck, Ch M; Schedel, A; Schilling, F H; Schmugge, M; Schneppenheim, R; Scholz, U; Scholz, T; Schulze, H; Siegemund, A; Strauß, G; Sykora, K-W; Wermes, C; Wiegering, V; Wieland, I; Zieger, B; Zotz, R B (2014). Therapie hereditärer Thrombozytopathien. Interdisziplinäre S2K-Leitlinie der Ständigen Kommission Pädiatrie der Gesellschaft für Thrombose- und Hämostaseforschung e. V. Hämostaseologie, 34(4):269-75, quiz 276.

This list was generated on Wed May 22 14:45:38 2019 CEST.