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Autor/in
- Budde, U
- Schneppenheim, Reinhard 10
- Obser, Tobias 6
- Castaman, G 4
- Oyen, Florian 4
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15 Einträge gefunden
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Homozygous type 2N R854W von Willebrand factor is poorly secreted and causes a severe von Willebrand disease phenotype.
2010 - Forschungsinformationssystem des UKE -
Shear-induced unfolding activates von Willebrand factor A2 domain for proteolysis.
2009 - Forschungsinformationssystem des UKE -
Response to DDAVP in children with von Willebrand disease type 2.
- Schneppenheim, Reinhard
- Budde, U
- Beutel, Karin
- Hassenpflug, W-A
- Hauch, H
- Obser, Tobias
- Oyen, Florian
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Acquired von Willebrand syndrome as side effect of valproic acid therapy in children is rare.
2009 - Forschungsinformationssystem des UKE -
Genetic defects in von Willebrand disease type 3 in Indian and Greek patients.
2008 - Forschungsinformationssystem des UKE -
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Gene conversions are a common cause of von Willebrand disease.
2005 - Forschungsinformationssystem des UKE -
[Thrombotic thrombocytopenic purpura in childhood]
2004 - Forschungsinformationssystem des UKE -
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