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Autor/in
- Schneppenheim, Reinhard
- Obser, Tobias 38
- Oyen, Florian 33
- Budde, Ulrich 20
- Budde, U 13
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110 Einträge gefunden
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Intracranial hemorrhage in a term newborn with severe von Willebrand disease type 3 associated with sinus venous thrombosis.
- Wetzstein, Viola
- Ulrich, Budde
- Oyen, Florian
- Ding, Xiaoqi
- Herrmann, Jochen
- Liebig, Birte
- Schneppenheim, Reinhard
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A91V is a polymorphism in the perforin gene not causative of an FHLH phenotype.
- Udo, Zur Stadt
- Beutel, Karin
- Weber, Belinda
- Kabisch, Hartmut
- Schneppenheim, Reinhard
- Janka-Schaub, Gritta
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Recombinant expression of mutations causing von Willebrand disease type Normandy: characterization of a combined defect of factor VIII binding and multimerization.
- Schneppenheim, Reinhard
- Lenk, Harald
- Obser, Tobias
- Oldenburg, Johannes
- Oyen, Florian
- Schneppenheim, Sonja
- Schwaab, Rainer
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Severe ADAMTS-13 deficiency in childhood.
2004 - Forschungsinformationssystem des UKE -
von Willebrand factor cleaving protease and ADAMTS13 mutations in childhood TTP.
- Schneppenheim, Reinhard
- Ulrich, Budde
- Oyen, Florian
- Angerhaus, Dorothea
- Aumann, Volker
- Drewke, Elke
- Hassenpflug, Wolf
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Molecular analysis of the SGLT2 gene in patients with renal glucosuria.
- Santer, René
- Kinner, Martina
- Lassen, Christoph L
- Schneppenheim, Reinhard
- Eggert, Paul
- Bald, Martin
- Brodehl, Johannes
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