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Journal Article
Haematologica (Roma), ISSN 1592-8721, 03/2008, Volume 93, Issue 3, pp. 372 - 380
Journal Article
British journal of haematology, ISSN 0007-1048, 11/2015, Volume 171, Issue 4, pp. 443 - 452
Summary Hereditary haemorrhagic telangiectasia is a rare systemic autosomal dominantly inherited disorder of the fibrovascular tissue with a wide variety of... 
Rendu‐Osler‐Weber disease | hereditary haemorrhagic telangiectasia | vascular malformation | anticoagulation | epistaxis | Rendu-Osler-Weber disease | Vascular malformation | Epistaxis | Anticoagulation | Hereditary haemorrhagic telangiectasia | Life Sciences & Biomedicine | Hematology | Science & Technology | Epistaxis - etiology | Telangiectasia, Hereditary Hemorrhagic - therapy | Humans | Antibiotic Prophylaxis | Telangiectasia, Hereditary Hemorrhagic - genetics | Embolization, Therapeutic | Thrombophilia - etiology | Telangiectasia, Hereditary Hemorrhagic - diagnosis | Fibrinolytic Agents - therapeutic use | Intracranial Arteriovenous Malformations - etiology | Thrombophilia - drug therapy | Telangiectasia, Hereditary Hemorrhagic - complications | Signal Transduction | Anemia, Iron-Deficiency - etiology | Arteriovenous Malformations - etiology | Transforming Growth Factor beta - physiology | Anticoagulants - therapeutic use | Epistaxis - prevention & control | Hemostatics - adverse effects | Liver - blood supply | Intracranial Arteriovenous Malformations - diagnosis | Gastrointestinal Hemorrhage - etiology | Neovascularization, Pathologic - drug therapy | Neovascularization, Pathologic - genetics | Disease Management | Hemostatics - therapeutic use | Lung - blood supply | Hypertension, Pulmonary - etiology | Telangiectasis | Index Medicus
Journal Article
Annals of internal medicine, ISSN 0003-4819, 08/2009, Volume 151, Issue 3, pp. 167 - 175
textabstractBackground: The Budd-Chiari syndrome (BCS) is hepatic venous outflow obstruction. What is known about the syndrome is based on small studies of... 
hyperhomocysteinemia | bleeding | major clinical study | Portugal | prothrombin | non invasive procedure | Behcet disease | ascites | overall survival | survival rate | esophagus varices | female | paroxysmal nocturnal hemoglobinuria | transjugular intrahepatic portosystemic shunt | treatment outcome | article | myeloproliferative disorder | protein C deficiency | Belgium | anticoagulant agent | hepatorenal syndrome | Budd Chiari syndrome | protein S deficiency | Italy | adolescent | antithrombin deficiency | adult | Germany | male | anticoagulation | protein S | follow up | Netherlands | abdominal pain | percutaneous transluminal angioplasty | phospholipid antibody | thrombosis | gastrointestinal hemorrhage | hepatic encephalopathy | antithrombin | blood clot lysis | priority journal | protein C | France | human | immunoglobulin G | gene mutation | cardiolipin antibody | aged | blood clotting factor 5 Leiden | United Kingdom | Switzerland | risk factor | Spain | diuretic agent | liver transplantation | Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Budd-Chiari Syndrome - etiology | Prospective Studies | Europe | Humans | Middle Aged | Risk Factors | Male | Treatment Outcome | Thrombophilia - complications | Angioplasty, Balloon, Coronary | Budd-Chiari Syndrome - therapy | Young Adult | Liver Transplantation - methods | Adolescent | Aged, 80 and over | Adult | Female | Aged | Myeloproliferative Disorders - complications | Portasystemic Shunt, Transjugular Intrahepatic | Budd-Chiari Syndrome - mortality | Causes of | Care and treatment | Research | Patient outcomes | Hepatic vein thrombosis | Patients | Hepatology | Medical treatment | Gastroenterology | Index Medicus | Abridged Index Medicus
Journal Article
Journal Article