Reinhard Schneppenheim
University Medical Center Hamburg-Eppendorf
Department of Pediatric Hematology and Oncology
Martinistrasse 52
D-20246 Hamburg
Germany
Name/email consistency: high
- A common origin of the 4143insA ADAMTS13 mutation. Schneppenheim, R., Kremer Hovinga, J.A., Becker, T., Budde, U., Karpman, D., Brockhaus, W., Hrachovinová, I., Korczowski, B., Oyen, F., Rittich, S., von Rosen, J., Tjønnfjord, G.E., Pimanda, J.E., Wienker, T.F., Lämmle, B. Thromb. Haemost. (2006)
- Phenotypic and genotypic diagnosis of von Willebrand disease: a 2004 update. Schneppenheim, R., Budde, U. Semin. Hematol. (2005)
- The evolving classification of von Willebrand disease. Schneppenheim, R. Blood Coagul. Fibrinolysis (2005)
- Recombinant expression of mutations causing von Willebrand disease type Normandy: characterization of a combined defect of factor VIII binding and multimerization. Schneppenheim, R., Lenk, H., Obser, T., Oldenburg, J., Oyen, F., Schneppenheim, S., Schwaab, R., Will, K., Budde, U. Thromb. Haemost. (2004)
- von Willebrand factor cleaving protease and ADAMTS13 mutations in childhood TTP. Schneppenheim, R., Budde, U., Oyen, F., Angerhaus, D., Aumann, V., Drewke, E., Hassenpflug, W., Häberle, J., Kentouche, K., Kohne, E., Kurnik, K., Mueller-Wiefel, D., Obser, T., Santer, R., Sykora, K.W. Blood (2003)
- Von Willebrand Disease type 2M "Vicenza" in Italian and German patients: identification of the first candidate mutation (G3864A; R1205H) in 8 families. Schneppenheim, R., Federici, A.B., Budde, U., Castaman, G., Drewke, E., Krey, S., Mannucci, P.M., Riesen, G., Rodeghiero, F., Zieger, B., Zimmermann, R. Thromb. Haemost. (2000)