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Barcella, Luca

About me

Name: Luca

Surname: Barcella

Academic title: MD

Link to personal website:

www.asst-pg23.it


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

  • Diagnostics
  • Treatment and care

Diseases:

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 acquired hemolytic anemia Paroxysmal nocturnal hemoglobinuria Typical hemolytic-uremic syndrome Autoimmune hemolytic anemia Autoimmune hemolytic anemia, cold type Cold agglutinin disease Paroxysmal cold hemoglobinuria Autoimmune hemolytic anemia, warm type Mixed-type autoimmune hemolytic anemia Drug-induced autoimmune hemolytic anemia Hemolytic disease due to fetomaternal alloimmunization Hemolytic disease of the newborn with Kell alloimmunization Rare hereditary hemochromatosis HFE related hereditary hemochromatosis (Symptomatic form of hemochromatosis type 1) - OMIM 235200 Hemochromatosis due to rare mutations in HFE (OMIM 235200)

Which is your patient age coverage?

  • Adults


Member Substitute

Member Go to member

Name english: Hospital Pope John XXIII - Bergamo

Name original: Ospedale Papa Giovanni XXIII di Bergamo


Healthcare provider Go to healthcare provider

Name english: Hospital Pope John XXIII - Bergamo

Name original: Ospedale Papa Giovanni XXIII di Bergamo

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