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Descripción paperback. Condición: New. Ship out in 2 business day, And Fast shipping, Free Tracking number will be provided after the shipment.Paperback. Pub Date: 2013 Pages: 165 Language: English Publisher: Science Press of Xiangya doctors experience Series: Department of Hematology and Oncology Clinical Experience one of the the Xiangya doctors experience Books aims to summarize and South Africa University Xiangya Hospital Department of Hematology and oncologists accumulation of years of clinical experience. and promote the exchange of experience of clinicians. thereby reducing the occurrence of medical errors and unnecessary losses. Good clinical experience. clinicians can be inspired to reflect on the flaws that may occur in the clinical diagnosis and treatment process. thereby increasing the level of clinical diagnosis and treatment. Xiangya the doctors experiences Series: Department of Hematology and Oncology Clinical Experience in close connection with the Department of Hematology and Oncology clinical practice. highly targeted and a high level of generality. help improve clinical hematologists and oncologists thinking capacity and disease diagnosis and treatment capacity available for hematologists and oncologists. graduate student use and reference. Contents: first Hematology Clinical Experience. Dimension A acid syndrome. Leukocyte stasis syndrome. Multiple factors induced coagulation disorders. Etiology of iron deficiency anemia treatment. The hypersplenism 6. Thrombotic thrombocytopenic purpura 7. epidemic hemorrhagic fever. lymphoma. rodenticide poisoning 10. diarrhea after hematopoietic stem cell transplantation 11. autoimmune hemolytic anemia 12. idiopathic thrombocytopenic purpura 13. multiple myeloma 14 original onset thrombocytosis disease 15. the allergic purpura 16. thrombotic thrombocytopenic purpura 17. polycythemia vera. 18 with acute lymphoblastic leukemia 19. multiple myeloma 20. autoimmune hemolytic anemia 21 iron deficiency anemia 22. acute lymphoblastic leukemia. 23 malignant histiocytosis 24 bone marrow metastases 25. lymphoma and skin and mucous membrane damage - paraneoplastic pemphigus 26. recurrent skin nodules - the primary subcutaneous fat film inflammation-like T-cell lymphoma 27. postoperative abdominal hematoma - Hemophilia 28 elderly patients with white blood cell count normal with severe anemia and thrombocytopenia - chronic lymphocytic leukemia 29 back hematoma and thrombocytosis - idiopathic thrombocytopenic histiocytosis 30 the joint immunosuppressive treatment of severe aplastic anemia 31 non-Hodgkin's lymphoma in the lungs diffuse disease and pleural fluid - pulmonary infiltrates 32. chronic hemophilic arthropathy 33. hemophilia Pseudotumor 34. Acquired hemophilia (non-hemophiliacs inhibitor) 35. hemophilia perioperative processing 36. Hemophilia physical therapy 37. hemophilia patients with inhibitors generated 38 female carriers of hemophilia bleeding tendency of 39 leukemia patients with pulmonary fungal infections 40. itraconazole antifungal therapy be anti cardiotoxicity 41 hereditary spherocytosis spherocytosis not necessarily Department of polycythemia 42 myelodysplastic syndrome diagnosis must be taken to exclude the tumor 43 other systems. Having strong anti-infection treatment of patients with diarrhea should be considered intestinal flora 44. breast metastasis cancer caused by anemia 45. Sjogren's syndrome due to thrombocytopenia 46 first biopsy failed Hodgkin lymphoma 47 elderly lymphoma patients with severe pulmonary infection without fever one case 48. acute blood stagnation recovery becomes acute leukemia in one case 49. multiple myeloma and renal insufficiency during the treatment of epilepsy in one case 50. clinical diagnosis and treatment of histoplasmosis experience 51. tumor with cold agglutinin syndrome 52. diagnosis and treatment of malignant proliferative diseases of the lymphatic system after 53. misdiagnosed as chronic lymphocytic leukemia. malignant proliferative diseases of the lymphatic syste. Nº de ref. del artículo: NE028904