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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 Rare anemia Rare hemolytic anemia Rare constitutional hemolytic anemia Lethal hemolytic anemia-genital anomalies syndrome Atypical hemolytic-uremic syndrome Atypical hemolytic-uremic syndrome with DGKE deficiency Atypical hemolytic-uremic syndrome with C3 anomaly Atypical hemolytic-uremic syndrome with MCP/CD46 anomaly Atypical hemolytic-uremic syndrome with B factor anomaly Atypical hemolytic-uremic syndrome with H factor anomaly Atypical hemolytic-uremic syndrome with I factor anomaly Atypical hemolytic-uremic syndrome with anti-factor H antibodies Atypical hemolytic-uremic syndrome with thrombomodulin anomaly Familial LCAT deficiency Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome Rare constitutional hemolytic anemia due to a red cell membrane anomaly Hereditary spherocytosis Hereditary elliptocytosis Distal renal tubular acidosis with anemia Hereditary stomatocytosis Overhydrated hereditary stomatocytosis Dehydrated hereditary stomatocytosis Rh deficiency syndrome Familial pseudohyperkalemia Southeast Asian ovalocytosis Hereditary cryohydrocytosis with reduced stomatin Hereditary cryohydrocytosis with normal stomatin Constitutional hemolytic anemia due to acanthocytosis Abetalipoproteinemia McLeod neuroacanthocytosis syndrome Primary CD59 deficiency Rare constitutional hemolytic anemia due to an enzyme disorder Congenital erythropoietic porphyria Hemolytic anemia due to hexose monophosphate shunt and glutathione metabolism anomalies Glutathione synthetase deficiency Glutathione synthetase deficiency with 5-oxoprolinuria Glutathione synthetase deficiency without 5-oxoprolinuria Gamma-glutamylcysteine synthetase deficiency Hemolytic anemia due to glutathione reductase deficiency 6-phosphogluconate dehydrogenase deficiency Hemolytic anemia due to a disorder of glycolytic enzymes Glycogen storage disease due to muscle phosphofructokinase deficiency Triose phosphate-isomerase deficiency Glycogen storage disease due to aldolase A deficiency Glycogen storage disease due to phosphoglycerate kinase 1 deficiency Hemolytic anemia due to red cell pyruvate kinase deficiency Hemolytic anemia due to glucophosphate isomerase deficiency Hemolytic anemia due to diphosphoglycerate mutase deficiency Non-spherocytic hemolytic anemia due to hexokinase deficiency Hemolytic anemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency Class I glucose-6-phosphate dehydrogenase deficiency Hemolytic anemia due to an erythrocyte nucleotide metabolism disorder Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency Hemolytic anemia due to adenylate kinase deficiency Hemolytic anemia due to erythrocyte adenosine deaminase overproduction Heinz body anemia Rare hereditary hemochromatosis HFE related hereditary hemochromatosis (Symptomatic form of hemochromatosis type 1) - OMIM 235200 Non-HFE related hereditary hemochromatosis Ferroportin Disease (Hemochromatosis type 4B) SLC40A1 related hereditary hemochromatosis - OMIM 606069 (Hemochromatosis type 4A)
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|English name||Original name||Subnetworks of expertise||Healthcare provider|
|Department of Oncology and Hematology - Immunohematology and Transfusion Medicine Unit||Dipartimento di Oncologia e Ematologia - Immunoematologia e Medicina Trasfusionale||Bleeding - Coagulation disorders, Haemochromatosis and other iron disorders||Hospital Pope John XXIII - Bergamo|