High‐affinity von Willebrand factor binding does not affect the anatomical or hepatocellular distribution of factor VIII in rats

Publisher： John Wiley & Sons Inc

E-ISSN： 1538-7836|14|9|1803-1813

ISSN： 1538-7933

Source： JOURNAL OF THROMBOSIS AND HAEMOSTASIS, Vol.14, Iss.9, 2016-09, pp. : 1803-1813

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Factor VIII-von Willebrand Factor Binding Defects in Autosomal Recessive von Willebrand Disease Type Normandy and in Mild Hemophilia A

By  

Acta Haematologica, Vol. 121, Iss. 2-3, 2009-06 ,pp. : 102-105

Karger

Access to resources Recommend Favorite

von Willebrand factor: factor VIII protector and friend

By  

JOURNAL OF THROMBOSIS AND HAEMOSTASIS, Vol. 10, Iss. 11, 2012-11 ,pp. : 2324-2327

John Wiley & Sons Inc

Access to resources Recommend Favorite

Factor VIII inhibitors: von Willebrand factor makes a difference in vitro and in vivo

By  

JOURNAL OF THROMBOSIS AND HAEMOSTASIS, Vol. 10, Iss. 11, 2012-11 ,pp. : 2328-2337

John Wiley & Sons Inc

Access to resources Recommend Favorite

6 Factor VIII Concentrates, Factor VIII/von Willebrand Factor Concentrates, Factor IX Concentrates, Activated Prothrombin Complex Concentrates

By  

Transfusion Medicine and Hemotherapy, Vol. 36, Iss. 6, 2009-12 ,pp. : 409-418

Karger

Access to resources Recommend Favorite

Managing Patients with von Willebrand Disease Type 1, 2 and 3 with Desmopressin and von Willebrand Factor-Factor VIII Concentrate in Surgical Settings

By  

Acta Haematologica, Vol. 121, Iss. 2-3, 2009-06 ,pp. : 167-176

Karger

Access to resources Recommend Favorite