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Platelet Disorders:     more books (54)

The Platelet and Its Disorders by B.G. Firkin, 1984-04-30 Platelets, Second Edition by Alan D. Michelson, 2006-10-26 Platelets in Hematologic and Cardiovascular Disorders: A Clinical Handbook Platelets in Thrombotic and Non-Thrombotic Disorders: Pathophysiology, Pharmacology and Therapeutics The Role of Platelet Activating Factor in Immune Disorders (New Trends in Lipid Mediators Research) (v. 2) Platelets and Their Factors Platelet-Dependent Vascular Occlusion (Annals of the New York Academy of Sciences) by Lisa K. Jennings, G. A. Fitzgerald, et all 1994-05 Platelet Protocols: Research and Clinical Laboratory Procedures by Melanie McCabe White, Lisa K. Jennings, 1999-03-12 Coagulation and Bleeding Disorders (Hematology) by T. S. Zimmerman, 1988-09-29 Platelet Immunology (Current Studies in Hematology and Blood Transfusion) Platelets in Biology and Pathology III (Research Monographs in Cell and Tissue Physiology) (v. 3) by D. Macintyre, 1987-01 Measurements of Platelet Function (Methods in Haematology) by Laurence A. Harker, 1984-07 The Platelets: Physiology and Pharmacology (Physiologic and Pharmacologic Bases of Drug Therapy) Platelet Disorders by Caen, 1991-03-13

lists with details

81. Press Releases Blood Center Researcher Wins Award From UW
    As part of the award, Dr. Drachman gave a presentation about his latestresearch on inherited platelet disorders. The presentation  
    http://www.psbc.org/community/press/press0049.htm

82. Platelet Immunology Laboratory Introduction
    antibodies in a variety of clinical conditions with the aim of improving the therapyavailable to patients with immunologicallymediated platelet disorders.  
    http://www.psbc.org/medical/labs/platelet/introduction.htm

83. Hematography Plus: Table Of Contents
    ATLAS OF NONMALIGNANT WBC AND platelet disorders Laboratory EvaluationInherited WBC Disorders Acquired WBC Disorders platelet disorders.  
    http://www1.umn.edu/hema/pages/toc.html
    
    Extractions: Each of the eight sections of H EMATOGRAPHY P LUS consists of a series of lessons. Most of the lessons, in turn, contain several topics. This Table of Contents shows you the section titles (in capital letters) and the lessons contained in each. Scroll down the list for a quick look at the entire contents of the H EMATOGRAPHY P LUS CD-ROM. I NTRODUCTION AND HELP

84. Diseases/Treatments In Hematology, Mayo Clinic In Rochester, Minn.
    hemoglobinuria; platelet disorders; Polycythemia rubra vera; Porphyria;Prolymphocytic leukemia; Qualitative (functional) platelet disorders;  
    http://www.mayoclinic.org/hematology-rst/diseases.html
    
    Extractions: search: Mayo Clinic Locations: Arizona Florida Minnesota Mayo Clinic ... Medical Specialties Hematology Hematology Overview Diseases/Treatments Treatment Groups Appointments ... All Medical Specialties - Rochester Acute lymphocytic leukemia Acute myelogenous leukemia Agnogenic myeloid metaplasia Amyloidosis Anemia and red cell disorders Anticoagulation disorders Autoimmune hemolytic anemias Autoimmune thrombocytopenia B-cell chronic lymphocytic leukemia Blood transfusion Castleman's disease Chronic lymphocytic leukemia Chronic myelogenous leukemia Chronic myelomonocytic leukemia Disorders of coagulation, bleeding, and clotting Essential thrombocythemia Hairy cell leukemia Hemoglobinopathies Hemophilias Hereditary hemolytic anemias Hodgkins disease ITP Large granular lymphocyte disorders Leukemias Leukopenia Lymphocytosis Lymphoma Macroglobulinemia Monoclonal gammopathy-associated conditions including c1-esterase inhibitor deficiency, cryoglobulinemia , osteosclerotic myeloma, peripheral neuropathy, POEMS syndrome , and systemic capillary leak syndrome Monoclonal gammopathy of undetermined significance Multiple myeloma and other protein disorders of the blood Myelodysplastic syndromes Myelofibrosis with myeloid metaplasia Myeloproliferative disorders Natural killer cell leukemia Non-Hodgkin's lymphoma Paroxysmal nocturnal hemoglobinuria Platelet disorders Polycythemia rubra vera Porphyria Prolymphocytic leukemia Qualitative (functional) platelet disorders Smoldering myeloma T-cell chronic lymphocytic leukemia Thalassemias Thrombocytopenia

85. ¼²²¡Ïà¹Ø
    Heparininduced thrombocytopenia; HIV-related thrombocytopenia; Humanizedmouse models of FcR clearance in immune platelet disorders;  
    http://cmbi.bjmu.edu.cn/news/insight/insight-dis.htm
    
    Extractions: Malaria Mitochondrial disease potential roles in embryogenesis and nucleocytoplasmic transfer A nuclear modifier for a mitochondrial DNA disorder Homoplasmic Mitochondrial DNA Diseases as the Paradigm to Understand the Tissue Specificity Beyond the Magic Circle ... Mitochondria, oxygen free radicals, and apoptosis

86. Platelet Function Disorders | Building Better Health
    There are several hereditary disorders characterized by some impairment of theplatelet's action. platelet disorders. British Medical Journal 314, no.  
    http://www.buildingbetterhealth.com/topic/topic100587311
    
    Extractions: Platelets are elements within the bloodstream that recognize and cling to damaged areas inside blood vessels. When they do this, the platelets trigger a series of chemical changes that result in the formation of a blood clot. There are certain hereditary disorders that affect platelet function and impair their ability to start the process of blood clot formation. One result is the possibility of excessive bleeding from minor injuries or menstrual flow. Description Platelets are formed in the bone marrowa spongy tissue located inside the long bones of the bodyas fragments of a large precursor cell (a megakaryocyte). These fragments circulate in the bloodstream and form the first line of defense against blood escaping from injured blood vessels. Damaged blood vessels release a chemical signal that increases the stickiness of platelets in the area of the injury. The sticky platelets adhere to the damaged area and gradually form a platelet plug. At the same time, the platelets release a series of chemical signals that prompt other factors in the blood to reinforce the platelet plug. Between the platelet and its reinforcements, a sturdy clot is created that acts as a patch while the damaged area heals. There are several hereditary disorders characterized by some impairment of the platelet's action. Examples include von Willebrand's disease, Glanzmann's thrombasthenia, and Wiskott-Aldrich syndrome. Vulnerable aspects of platelet function include errors in the production of the platelets themselves or errors in the formation, storage, or release of their chemical signals. These defects can prevent platelets from responding to injuries or from prompting the action of other factors involved in clot formation.

87. Best Practice & Research Clinical Haematology
    Volume 2 1989 1 Aplastic Anaemia EC GordonSmith 2 Iron Chelating Therapy C Hershko3 platelet disorders JP Caen 4 The Molecular Biology of Coagulation EGD  
    http://www.elsevier-international.com/journals/beha/supp.cfm?ID=130

88. ACQUIRED BLEEDING DISORDERS
    An article by Thomas G. DeLoughery, Associate Professor of Medicine. platelet transfusion therapy and dysfunctional platelets are discussed.  
    http://www.ohsu.edu/som-hemonc/handouts/deloughery/bleed.shtml
    
    Extractions: ACQUIRED BLEEDING DISORDERS THROMBOCYTOPENIA Thrombocytopenia is a relatively common finding in the hospital setting. Finding the etiology is frustrating as multiple factors may be producing the thrombocytopenia. A rational approach is to consider the differential from a mechanistic point of view. Thus defects in platelet production, increased platelet sequestration or increased platelet destruction (immune or non-immune) can lead to thrombocytopenia. Decreased production: So-called "acquired amegakaryocytic thrombocytopenia" is relatively rare. The leading cause is heavy (fifth/day) use of alcohol which leads to a megakaryocytic maturation defect. Clinically the platelets are small (MPV low) and the count remains depresses for 3-5 days after stopping alcohol but then rapidly rises with a "rebound" thrombocytosis. Thiazides and tegratol may be also associated with decreased production. Late-stage HIV patients may have prolonged thrombocytopenia with pyrimethamine and other medicines. Sequestration: Splenomegaly due to any cause can lead to thrombocytopenia. Usually the platelet count is not below 50,000/cm

89. Platelet Funct. Disorders TOH19
    platelet Function disorders. Amy Shapiro. 19 Published in 1999. Keywords plateletdisorders; von Willebrand disease (vWD). Treatment of Hemophilia, No.  
    http://www.wfh.org/ShowDoc.asp?Rubrique=31&Document=238

90. NHF | Resources | Nurses
    of coagulation disorders. (Review). American Journal of Obstetrics Gynecology175 (3 Pt 2) 778783, September. 8. Rodgers, GM (1999). Overview of platelet  
    http://www.hemophilia.org/resources/nurses/bibliography.htm

91. Hemophilia
    platelet Function disorders. platelet Function disorders. Introduction. Symptoms.Diagnosis. platelet Function disorders. Women With Inherited Bleeding disorders.  
    http://www.hemophilia.ca/en/2.4.html

92. HONselect - Hematologic Diseases
    Hematologic Diseases. MeSH definition disorders of the blood and bloodforming tissues. Subheadings complications / diagnosis / embryology  
    http://www.hon.ch/HONselect/Selection/C15.378.html
    
    Extractions: HONselect: Introduction Search Browse Favourites List of Rare Disease add HONselect Contents on "Hematologic Diseases": MeSH hierarchy and definition Research Articles Web resources Medical Images Medical News Medical Conferences Clinical Trials Wondering about the holiday blues! MeSH Hierarchy English French German Spanish Portuguese MeSH Broader term(s) Diseases MeSH Narrow term(s) Anemia Blood Coagulation Disorders Blood Group Incompatibility Blood Platelet Disorders Blood Protein Disorders Bone Marrow Diseases Hematologic Neoplasms Hemoglobinopathies Hemorrhagic Disorders Leukocyte Disorders Thrombophilia Erythrocyte Aggregation, Intravascular Methemoglobinemia Pancytopenia Polycythemia Pregnancy Complications, Hematologic Preleukemia Sulfhemoglobinemia Accepted term(s)

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