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):
Von Willebrand disease, Von Willebrand factor, molecular genetics
Hereditary thrombocytopenia with early-onset myelofibrosis Gaisböck syndrome Rare coagulation disorder 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 Rare hemorrhagic disorder due to a platelet anomaly Rare hemorrhagic disorder due to a constitutional platelet anomaly Rare hemorrhagic disorder due to a constitutional thrombocytopenia Syndromic constitutional thrombocytopenia Stormorken-Sjaastad-Langslet syndrome Thrombocytopenia-absent radius syndrome Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome MYH9-related disease GNE myopathy Jacobsen syndrome Macrothrombocytopenia with mitral valve insufficiency Alpha delta granule deficiency Dense granule disease Wiskott-Aldrich syndrome Chédiak-Higashi syndrome Hereditary thrombocytopenia with normal platelets-hematological cancer predisposition syndrome Hermansky-Pudlak syndrome Hermansky-Pudlak syndrome with neutropenia Hermansky-Pudlak syndrome with pulmonary fibrosis Hermansky-Pudlak syndrome without pulmonary fibrosis Hermansky-Pudlak syndrome type 7 Hermansky-Pudlak syndrome type 8 Hermansky-Pudlak syndrome type 9 Isolated constitutional thrombocytopenia Isolated hereditary giant platelet disorder Severe autosomal recessive macrothrombocytopenia Bernard-Soulier syndrome Thrombocytopenia with congenital dyserythropoietic anemia Autosomal dominant macrothrombocytopenia Alpha granule disease Gray platelet syndrome Quebec platelet disorder Medich giant platelet syndrome White platelet syndrome Paris-Trousseau thrombocytopenia X-linked dyserythropoetic anemia with abnormal platelets and neutropenia Hereditary thrombocytopenia with normal platelets X-linked thrombocytopenia with normal platelets Autosomal thrombocytopenia with normal platelets Congenital amegakaryocytic thrombocytopenia Bleeding diathesis due to thromboxane synthesis deficiency Isolated delta-storage pool disease Autosomal dominant thrombocytopenia with platelet secretion defect Rare hemorrhagic disorder due to a qualitative platelet defect Glanzmann thrombasthenia Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder Ehlers-Danlos syndrome, fibronectinemic type Scott syndrome P2Y12 defect Pseudo-von Willebrand disease Bleeding diathesis due to a collagen receptor defect Bleeding diathesis due to glycoprotein VI deficiency Bleeding diathesis due to integrin alpha2-beta1 deficiency Bleeding disorder due to CalDAG-GEFI deficiency Rare hemorrhagic disorder due to an acquired platelet anomaly Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome TAFRO syndrome HELLP syndrome Fetal and neonatal alloimmune thrombocytopenia Autoimmune thrombocytopenia Immune thrombocytopenic purpura Evans syndrome STAT3-related early-onset multisystem autoimmune disease Kasabach-Merritt syndrome
Which is your patient age coverage?
|English name||Original name||Subnetworks of expertise||Healthcare provider|
|Department on Thrombosis and Hemostasis||Afdeling Trombose en Hemostase||Bleeding - Coagulation disorders||Leiden University Medical Center|