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Autor/in
- Budde, U
- Schneppenheim, Reinhard 13
- Schneppenheim, R 12
- Castaman, G 7
- Obser, Tobias 7
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27 Einträge gefunden
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Identification and characterization of the elusive mutation causing the historical von Willebrand Disease type IIC Miami
2016 - Forschungsinformationssystem des UKE -
von Willebrand disease type 2A phenotypes IIC, IID and IIE: A day in the life of shear-stressed mutant von Willebrand factor
2014 - Forschungsinformationssystem des UKE -
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Reduced von Willebrand factor secretion is associated with loss of Weibel-Palade body formation.
- Castaman, G
- Giacomelli, S H
- Jacobi, P M
- Obser, Tobias
- Budde, U
- Rodeghiero, F
- Schneppenheim, Reinhard
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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 -
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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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Shear-induced unfolding activates von Willebrand factor A2 domain for proteolysis.
2009 - Forschungsinformationssystem des UKE -
Acquired von Willebrand syndrome as side effect of valproic acid therapy in children is rare.
2009 - Forschungsinformationssystem des UKE -
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Genetic defects in von Willebrand disease type 3 in Indian and Greek patients.
2008 - Forschungsinformationssystem des UKE -