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Nume Sagittal Sinus Thrombosis
Pagina Web www.malacards.org
Clasificare anatomică Malacards Boli cardiovasculare; Boli de sânge

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Boli A-Z Abducens Nerve Disease Acquired Hemophilia Acquired Hemophilia a Acquired Immunodeficiency Syndrome Acute Liver Failure Adenocarcinoma Afibrinogenemia Afibrinogenemia, Congenital Alcohol-Related Birth Defect Alpha-2-Plasmin Inhibitor Deficiency Analbuminemia Aneurysm Angina Pectoris Aniridia 1 Anorexia Nervosa 1 Anterior Cranial Fossa Meningioma Anterior Spinal Artery Syndrome Antiphospholipid Syndrome Antithrombin Iii Deficiency Aplasia Cutis Congenita Aplastic Anemia Arteriovenous Fistula Arteritic Anterior Ischemic Optic Neuropathy B-Cell Lymphomas Bleeding Disorder, Platelet-Type, 11 Blood Coagulation Disease Blood Group--Ahonen Blood Group, I System Blood Platelet Disease Blood Protein Disease Blue Toe Syndrome Branch Retinal Artery Occlusion Budd-Chiari Syndrome Catastrophic Antiphospholipid Syndrome Cellulitis Central Retinal Vein Occlusion Cerebral Falx Meningioma Cerebral Hemorrhage Cerebral Sinovenous Thrombosis Cerebritis Cervical Adenocarcinoma Cervicitis Chops Syndrome Colitis Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Coronary Thrombosis Cortical Blindness Cryptogenic Cirrhosis Disseminated Intravascular Coagulation Down Syndrome Dysfibrinogenemia Eclampsia Endocardium Disease Esophageal Varix Evans' Syndrome Factor V Deficiency Factor Vii Deficiency Factor Viii Deficiency Factor X Deficiency Factor Xi Deficiency Factor Xii Deficiency Factor Xiii Deficiency Femoral Neuropathy Fournier Gangrene Frontal Sinusitis Giant Hemangioma Glanzmann Thrombasthenia Hantavirus Pulmonary Syndrome Headache Head Injury Hellp Syndrome Hemoglobin E Disease Hemoglobinuria Hemophilia Hemophilia a Hemophilia B Hemorrhagic Disease Hemorrhagic Fever Heparin-Induced Thrombocytopenia Hepatic Infarction Hepatic Vascular Disease Hepatic Veno-Occlusive Disease Hepatitis a Homocysteinemia Homocystinuria Hydrocephalus Hypersplenism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hyperthyroidism Immune System Disease Inherited Blood Coagulation Disease Intermediate Coronary Syndrome Intermittent Claudication Intestinal Impaction Intracranial Embolism Intracranial Hypertension Intracranial Hypotension Intracranial Sinus Thrombosis Intracranial Thrombosis Intravascular Large B-Cell Lymphoma Ischemic Colitis Ischemic Optic Neuropathy Korean Hemorrhagic Fever Leech Infestation Legg-Calve-Perthes Disease Leukemia Livedoid Vasculopathy Lupus Erythematosus Lymphoblastic Leukemia Lymphoblastic Lymphoma Lymphoma Mantle Cell Lymphoma Marantic Endocarditis Medulloblastoma Meningococcemia Myelodysplastic Syndrome Myeloid Leukemia Nephrotic Syndrome Nonarteritic Anterior Ischemic Optic Neuropathy Osteonecrosis Papilledema Paracetamol Poisoning Paraneoplastic Syndromes Paroxysmal Nocturnal Hemoglobinuria Patent Foramen Ovale Peripheral Vertigo Placenta Disease Placental Abruption Placental Insufficiency Porencephaly Portal Vein Thrombosis Post-Thrombotic Syndrome Pre-Eclampsia Protein C Deficiency Protein S Deficiency Prothrombin Deficiency Prothrombin Deficiency, Congenital Pulmonary Embolism Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pulmonary Immaturity Purpura Purpura Fulminans Qualitative Platelet Defect Retinal Artery Occlusion Retinal Vascular Occlusion Retinal Vein Occlusion Scott Syndrome Severe Hemophilia a Severe Pre-Eclampsia Sinusitis Sneddon Syndrome Spinal Cord Infarction Splenic Disease Spontaneous Intracranial Hypotension Squamous Cell Papilloma Sticky Platelet Syndrome Stroke, Ischemic Subendocardial Myocardial Infarction Sudden Sensorineural Hearing Loss Systemic Lupus Erythematosus Tetralogy of Fallot Thrombasthenia Thrombocytopenia Thrombocytosis Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Trichinosis Typhoid Fever Ulcerative Colitis Varicose Veins Vein Disease Ventricular Fibrillation, Paroxysmal Familial, 1 Von Willebrand's Disease Von Willebrand Disease, Type 1