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10.1111/ijlh.12345 http://scihub22266oqcxt.onion/10.1111/ijlh.12345 C5600156!5600156 !25976955     free     free     free Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\25976955 .jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       Int+J+Lab+Hematol 2015 ; 37 Suppl 1 (Suppl 1 ): 11-7 Nephropedia Template TP {{tp|p=25976955 |t=2015. Laboratory diagnosis of von Willebrand disease |pdf=|usr=}}{{25976955 }} gab.com Text Laboratory diagnosis of von Willebrand disease JO: Int J Lab Hematol http://www.kidney.de/pget.php?&tw=1&pmid=25976955 #FOAvip Von Willebrand disease (VWD) is considered the most common inherited bleeding disorder and may also be the most difficult to diagnose. Clinical symptoms of VWD include predominantly mild mucosal bleeding; surgical bleeding may occur with specific challenges and joint bleeding can occur in the most severe forms. A family history either of diagnosed VWD or of bleeding symptoms is typically present. Laboratory diagnosis requires a series of assays of von Willebrand factor (VWF) quantity and function, and factor VIII activity, with no single straightforward diagnostic test available to either confirm or exclude the diagnosis. Newer assays of VWF function are becoming more available and useful in determining the laboratory diagnosis of VWD. Twit Text FOAVip Laboratory diagnosis of von Willebrand disease ????Int J Lab Hematol http://www.kidney.de/pget.php?&tw=1&pmid=25976955 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=25976955 #FOAvip English Wikipedia <ref>{{Cite pmid|25976955 }}</ref> Laboratory diagnosis of von Willebrand disease #MMPMID25976955 Roberts JC ; Flood VH Int J Lab Hematol 2015[May]; 37 Suppl 1 (Suppl 1 ): 11-7 PMID25976955 show ga Von Willebrand disease (VWD) is considered the most common inherited bleeding disorder and may also be the most difficult to diagnose. Clinical symptoms of VWD include predominantly mild mucosal bleeding; surgical bleeding may occur with specific challenges and joint bleeding can occur in the most severe forms. A family history either of diagnosed VWD or of bleeding symptoms is typically present. Laboratory diagnosis requires a series of assays of von Willebrand factor (VWF) quantity and function, and factor VIII activity, with no single straightforward diagnostic test available to either confirm or exclude the diagnosis. Newer assays of VWF function are becoming more available and useful in determining the laboratory diagnosis of VWD. |Clinical Laboratory Techniques/*methods [MESH] |Factor VIII/*metabolism [MESH] |Humans [MESH] |Reproducibility of Results [MESH] |Ristocetin/metabolism [MESH] |Sensitivity and Specificity [MESH] |von Willebrand Diseases/blood/classification/*diagnosis [MESH]Laboratory diagnosis of von Willebrand disease (epmc).pdf DeepDyve Pubget Overpricing