Academic title: MD PhD
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Which is your area of expertise for the "Disease/group of diseases"?
Specify your expertise for the "Disease/group of diseases" (eg SCT, Molecular diagnosis):
Gene therapy for haemophilia
Gaisböck syndrome Rare thrombotic disease of hematologic origin Rare thrombotic disorder due to a coagulation factors defect Rare thrombotic disorder due to a constitutional coagulation factors defect Congenital factor XII deficiency Familial thrombomodulin anomalies Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency Rare hereditary thrombophilia Hereditary thrombophilia due to congenital protein S deficiency Hereditary thrombophilia due to congenital protein C deficiency Hereditary thrombophilia due to congenital antithrombin deficiency Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency Rare thrombotic disorder due to an acquired coagulation factors defect Catastrophic antiphospholipid syndrome Heparin-induced thrombocytopenia Protein S acquired deficiency Acquired purpura fulminans Simple cryoglobulinemia Rare hemorrhagic disorder Rare hemorrhagic disorder due to a coagulation factors defect Rare hemorrhagic disorder due to a constitutional coagulation factors defect Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome Hemophilia Hemophilia A Severe hemophilia A Moderately severe hemophilia A Mild hemophilia A Symptomatic form of hemophilia A in female carriers Hemophilia B Severe hemophilia B Moderately severe hemophilia B Mild hemophilia B Symptomatic form of hemophilia B in female carriers Congenital factor V deficiency Congenital fibrinogen deficiency Familial afibrinogenemia Familial dysfibrinogenemia Familial hypofibrinogenemia Familial hypodysfibrinogenemia Congenital alpha2-antiplasmin deficiency Congenital factor XIII deficiency Von Willebrand disease Von Willebrand disease type 1 Von Willebrand disease type 2 Von Willebrand disease type 2A Von Willebrand disease type 2B Von Willebrand disease type 2M Von Willebrand disease type 2N Von Willebrand disease type 3 Congenital factor XI deficiency Congenital plasminogen activator inhibitor type 1 deficiency Congenital high-molecular-weight kininogen deficiency Congenital prekallikrein deficiency Combined deficiency of factor V and factor VIII Congenital vitamin K-dependent coagulation factors deficiency Congenital factor VII deficiency Congenital factor II deficiency Congenital factor X deficiency Hereditary combined deficiency of vitamin K-dependent clotting factors Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation East Texas bleeding disorder Thrombomodulin-related bleeding disorder Rare hemorrhagic disorder due to an acquired coagulation factor defect Acquired prothrombin deficiency Acquired hemophilia Acquired von Willebrand syndrome
Which is your patient age coverage?
|English name||Original name||Subnetworks of expertise||Healthcare provider|
|Internal Medicine, vascular medicine||Interne geneeskunde, vasculaire geneeskunde||Bleeding - Coagulation||Academic Medical Center Amsterdam|