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1. Full Text Hereditary Thrombotic Thrombocytopenic Purpura
by Kremer Hovinga, Johanna A and George, James N
The New England journal of medicine, ISSN 0028-4793, 10/2019, Volume 381, Issue 17, pp. 1653 - 1662
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Purpura, Thrombotic Thrombocytopenic - history | Plasma | Diagnosis, Differential | Prevalence | History, 20th Century | Humans | Male | Plasma Exchange | Purpura, Thrombotic Thrombocytopenic - diagnosis | Genes, Recessive | ADAMTS13 Protein - metabolism | Blood Component Transfusion | ADAMTS13 Protein - genetics | ADAMTS13 Protein - deficiency | Female | Purpura, Thrombotic Thrombocytopenic - therapy | Mutation | Purpura, Thrombotic Thrombocytopenic - genetics | Thrombocytopenic purpura | Outcome and process assessment (Health Care) | Care and treatment | Analysis | Risk factors | Blood transfusions | Health care | Pathogenesis | Thrombosis | Clotting | Hereditary diseases | Proteins | Thrombotic thrombocytopenic purpura | Hospitals | Blood platelets | Purpura | Von Willebrand factor | Health risk assessment | Binding sites | Index Medicus | Abridged Index Medicus
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2. Full Text Consensus on the standardization of terminology in thrombotic thrombocytopenic purpura and related thrombotic microangiopathies
by Scully, M and Cataland, S and Coppo, P and Rubia, J and Friedman, K. D and Kremer Hovinga, J and Lämmle, B and Matsumoto, M and Pavenski, K and Sadler, E and Sarode, R and Wu, H and Gale, D and Fujimura, Y and McDonald, V and Peyvandi, F and Scharrer, I and Veyradier, A and Westwood, J. P and Int Working Grp Thrombotic and International Working Group for Thrombotic Thrombocytopenic Purpura and the International Working Group for Thrombotic Thrombocytopenic Purpura
Journal of thrombosis and haemostasis, ISSN 1538-7933, 02/2017, Volume 15, Issue 2, pp. 312 - 322
diagnosis, differential | thrombotic thrombocytopenic purpura | thrombotic microangiopathy | thrombocytopenia | ADAMTS‐13 protein, human | ADAMTS-13 protein, human | Peripheral Vascular Disease | Life Sciences & Biomedicine | Hematology | Cardiovascular System & Cardiology | Science & Technology | Recurrence | Humans | ADAMTS13 Protein - blood | Fibrin - chemistry | Societies, Medical | Adult | Female | Hemolytic-Uremic Syndrome - diagnosis | Child | von Willebrand Factor - metabolism | Hemolysis | Diagnosis, Differential | Hematology - standards | Terminology as Topic | Treatment Outcome | Inflammation | Purpura, Thrombotic Thrombocytopenic - diagnosis | Remission Induction | Consensus | Complement System Proteins | Platelet Aggregation | Pregnancy | Platelet Count | Blood Platelets - metabolism | Erythrocytes - metabolism | Thrombotic Microangiopathies - diagnosis | Thrombocytopenic purpura | Enzymes | Terms and phrases | Anemia | Liver | Von Willebrand factor | Working groups | Standardization | Thrombocytopenia | Thrombotic microangiopathy | Clinical trials | Disseminated intravascular coagulation | Transplantation | Thrombotic thrombocytopenic purpura | Hemolytic anemia | Purpura | Remission | Platelets | Autoimmune diseases | Index Medicus
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3. Full Text Guidelines on the diagnosis and management of thrombotic thrombocytopenic purpura and other thrombotic microangiopathies
by Scully, Marie and Hunt, Beverley J and Benjamin, Sylvia and Liesner, Ri and Rose, Peter and Peyvandi, Flora and Cheung, Betty and Machin, Samuel J and British Comm Stand Haematology and British Committee for Standards in Haematology and on behalf of British Committee for Standards in Haematology
British journal of haematology, ISSN 0007-1048, 08/2012, Volume 158, Issue 3, pp. 323 - 335
guidelines | thrombotic thrombocytopenic purpura | thrombotic microangiopathy | Thrombotic microangiopathy | Thrombotic thrombocytopenic purpura | Guidelines | Life Sciences & Biomedicine | Hematology | Science & Technology | Hematologic and hematopoietic diseases | Anemias. Hemoglobinopathies | Biological and medical sciences | Medical sciences | Diseases of red blood cells | Platelet diseases and coagulopathies | Pregnancy | Diagnosis, Differential | Purpura, Thrombotic Thrombocytopenic - pathology | Thrombotic Microangiopathies - pathology | Humans | Thrombotic Microangiopathies - therapy | Female | Male | Thrombotic Microangiopathies - diagnosis | Purpura, Thrombotic Thrombocytopenic - therapy | Purpura, Thrombotic Thrombocytopenic - diagnosis | Thrombocytopenic purpura | Practice guidelines (Medicine) | Care and treatment | Diagnosis | Index Medicus
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4. Full Text Thrombotic thrombocytopenic purpura
by Kremer Hovinga, Johanna A and Coppo, Paul and Lämmle, Bernhard and Moake, Joel L and Miyata, Toshiyuki and Vanhoorelbeke, Karen
Nature reviews. Disease primers, ISSN 2056-676X, 04/2017, Volume 3, Issue 1, pp. 17020 - 17020
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Antiviral Agents - pharmacology | Glucocorticoids - therapeutic use | Pregnancy Complications - etiology | Antiviral Agents - therapeutic use | Immunomodulation | Humans | ADAMTS13 Protein - analysis | Purpura, Thrombotic Thrombocytopenic - complications | Purpura, Thrombotic Thrombocytopenic - diagnosis | ADAMTS13 Protein - blood | Splenectomy - methods | Pregnancy | Rituximab - pharmacology | Rituximab - therapeutic use | HIV Infections - etiology | Shiga Toxins - adverse effects | Acetylcysteine - pharmacology | Glucocorticoids - pharmacology | Female | Acetylcysteine - therapeutic use | Purpura, Thrombotic Thrombocytopenic - physiopathology | Immunologic Factors - pharmacology | Immunologic Factors - therapeutic use | Index Medicus
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5. Full Text Thrombotic thrombocytopenic purpura: pathogenesis, diagnosis and potential novel therapeutics
by Saha, M and McDaniel, J. K and Zheng, X. L
Journal of thrombosis and haemostasis, ISSN 1538-7933, 10/2017, Volume 15, Issue 10, pp. 1889 - 1900
diagnosis | therapeutics | pathology | thrombotic microangiopathies | von Willebrand factor | Peripheral Vascular Disease | Life Sciences & Biomedicine | Hematology | Cardiovascular System & Cardiology | Science & Technology | Recombinant Proteins - therapeutic use | Genetic Therapy | Predictive Value of Tests | Autoantibodies - blood | Humans | Plasma Exchange | ADAMTS13 Protein - blood | ADAMTS13 Protein - immunology | Hemostasis | Immunotherapy | Thrombocytopenia - therapy | Diagnosis, Differential | ADAMTS13 Protein - therapeutic use | Risk Factors | Treatment Outcome | Purpura, Thrombotic Thrombocytopenic - diagnosis | Purpura, Thrombotic Thrombocytopenic - epidemiology | Thrombocytopenia - blood | ADAMTS13 Protein - genetics | Anemia, Hemolytic - therapy | Anemia, Hemolytic - diagnosis | Thrombocytopenia - diagnosis | Purpura, Thrombotic Thrombocytopenic - therapy | Anemia, Hemolytic - blood | Purpura, Thrombotic Thrombocytopenic - blood | Autoimmunity | Autoantibodies | Anemia | Development and progression | Homeopathy | Materia medica and therapeutics | Thrombocytopenic purpura | Haptoglobin | Therapeutics | Von Willebrand factor | Hemoglobin | Diagnosis | Health aspects | Corticoids | Plasma | Cyclosporins | Pathogenesis | Prophylaxis | Antagonists | Splenectomy | Hemolytic anemia | Remission | Metalloproteinase | Thrombocytopenia | Thrombotic microangiopathy | Hemolytic uremic syndrome | Immunomodulation | Rituximab | Morbidity | L-Lactate dehydrogenase | Cyclophosphamide | Purpura | Lactic acid | Gene therapy | Platelets | Index Medicus | Pathology | Thrombotic Microangiopathies | von Willebrand Factor
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