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Thrombocytopenia

), secondary immune thrombocytopenias, myelodysplastic syndromes with thrombocytopenia, bone marrow failure syndromes and non-immune thrombocytopenias;

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Thrombocytopenia

millionth of a litre) of blood. Platelet counts less than 150,000 are termed thrombocytopenia. Platelet counts greater that 450,000 are called;

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Hemolytic Uremic Syndrome

Hemolytic uremic syndrome (HUS) is characterized by the triad non-immune micro-angiopathic hemolytic anaemia, thrombocytopenia and acute;

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Thrombotic Thrombocytopenic Purpura

platelet agglutination, organ ischaemia, severe thrombocytopenia and fragmentation of red blood cells. In the opening study included in Thrombotic;

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Heparin-Induced Thrombocytopenia

Although first reported in 1973, immune heparin-induced thrombocytopenia (HIT) remains one of the most frequent and devastating adverse;

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Chronic Immune Thrombocytopenia, An Issue of Hematology/Oncology Clinics of North America

Chronic immune thrombocytopenia is a disease in which the immune system destroys platelets (blood cells involved in the clotting process;

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Consultative Hematology, An Issue of Hematology/Oncology Clinics of North America

have Thrombocytopenia?;

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Surgical Critical Care, An Issue of Surgical Clinics

An important review on critical care for the general surgeon! Topics include: heparin induced thrombocytopenia, monitoring devices;

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Venous Thromboembolism In Critical Care, An Issue Of Critica

;Catheter and Surgical Thromboembolectomy;Vena Caval Interruption;New Anti-Coagulants;Heparin Induced Thrombocytopenia;

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Coagulation/Endothelial Dysfunction ,An Issue of Critical Care Clinics

thrombocytopenia and Disseminated intravascular coagulation in the critically ill; Thrombocytopenia associated multiple organ failure (TAMOF;

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Stem Cells Origins of Cytokine Interactions

erythrocytes to treat thrombocytopenia are herein reported.HSCs respond to the growth factors and the herbal medicine is a welcome substitute with lack;

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Hematologic Diseases, An Issue of Primary Care: Clinics in Office Practice

Diseases. Articles in this issue include: Anemia; Thrombocytopenia; Leukopenia and Pancytopenia; Leukocytosis and Leukemia; Polycythemia and;

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Disorders of the Platelets, An Issue of Hematology/Oncology Clinics of North America

, Congenital Thrombocytopenias, Immune Thrombocytopenias, Heparin Induced Thrombocytopenia, and Functional defects: Chronic granulomatous disease (CGD;

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Nonmalignant Hematology, An Issue of Critical Care Clinics

Topics include: A Critical re-appraisal of Factor VIIa; Thrombocytopenia: Hit vs non-HIT causes; Transfusion Reactions: Newer concepts on;

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Practical Phlebology

thrombolysis Inferior vena cava filters Heparin-induced thrombocytopenia Femoral endovenectomy and endoluminal;

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Clinical Thrombosis

thrombosis such as Protein C and S deficiency, lupus anticoagulants, immune heparin-induced thrombocytopenia, new diagnostic techniques and newer;

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Alloimmune Disorders of Pregnancy

Collectively known as the alloimmune cytopenias, hemolytic disease of the fetus and newborn, alloimmune thrombocytopenia and alloimmune;

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Alloimmune Disorders of Pregnancy

Collectively known as the alloimmune cytopenias, hemolytic disease of the fetus and newborn, alloimmune thrombocytopenia and alloimmune;

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Pediatric Thrombotic Disorders

; heparin-induced thrombocytopenia/thrombosis syndrome; venous thromboembolism prevention; thrombolysis; and novel anticoagulants, among others;

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Medically Challenging Patients Undergoing Cardiothoracic Surgery

considerations for patients with heparin-induced thrombocytopenia, pregnant patients requiring cardiac surgery with cardiopulmonary bypass, and obese;

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Antibody Therapy

of immunomodulatory IgG treatment in the bleeding disorder immune thrombocytopenia (ITP). Finally, the transition from polyclonal to monoclonal antibody (mAb;

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Hematology

of splenomegaly, indications for splenectomy, differential diagnosis of normocytic anemia, macrocytic anemia, hypochromic anemia, thrombocytopenia, bone;

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Consultations in Liver Disease,An Issue of Clinics in Liver Disease

. Specific areas addressed include the following: Management of esophageal and gastric varices; Severe thrombocytopenia in chronic liver disease and;

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Immune Hematology

, presentation, evaluation, and treatment strategies for immune thrombocytopenia (ITP), the most common cause of antibody-mediated platelet destruction;

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Immunohematology and Transfusion Medicine

, heparin-induced thrombocytopenia, and the approach to the bloodless patient. Written by experts in the field, Immunohematology and Transfusion;

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Horizons in Cancer Research

of tumor-associated thrombocytopenia by quercetin. Chapter Nine examines robotic surgery for prostate cancer.;

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Advances in Health and Disease

disorders. Chapter Four discusses the incidence and prognostic significance of sepsis-associated thrombocytopenia, summarizes the possible;

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