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Gouw, Samantha

About me

Name: Samantha

Surname: Gouw

Academic title: MD PhD

Which is your area of expertise for the "Disease/group of diseases"?

  • Diagnostics
  • Treatment and care


Rare coagulation disorder 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 anemia Hemoglobinopathy Sickle cell disease and related diseases Sickle cell anemia Sickle cell disease associated with an other hemoglobin anomaly Sickle cell-beta-thalassemia disease syndrome Sickle cell-hemoglobin C disease syndrome Sickle cell-hemoglobin D disease syndrome Sickle cell-hemoglobin E disease syndrome Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome

Which is your patient age coverage?

  • Pediatrics

Member Go to member

Name english: Academic Medical Center Amsterdam

Name original: Academic Medical Center Amsterdam

Healthcare provider Go to healthcare provider

Name english: Academic Medical Center Amsterdam

Name original: Academic Medical Center Amsterdam


English name Original name Subnetworks of expertise Healthcare provider