Results 251 to 260 of about 1,171,277 (292)
Overwhelming Post‐Splenectomy Sepsis From Capnocytophaga canimorsus
International Journal of Laboratory Hematology, EarlyView.
Maitlyn Hsia +3 more
wiley +1 more source
Expert Review of Hematology, 2021 Tato práce je věnována imunitní trombocytopenii. Zabývá se její historií, popisem základních struktur, dějů a částí v lidském organismu, které jsou potřebné k pochopení průběhu tohoto onemocnění.
James Bruce Bussel +2 more
exaly +7 more sources
Hematology/Oncology Clinics of North America, 2013 Immune thrombocytopenia (ITP) is a common hematologic disorder characterized by isolated thrombocytopenia. ITP presents as a primary or a secondary form. ITP may affect individuals of all ages, with peaks during childhood and in the elderly, in whom the age-specific incidence of ITP is greatest. Bleeding is the most common clinical manifestation of ITP.
Keith R McCrae
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Immune Thrombocytopenia in Pregnancy [PDF]
Hematology/Oncology Clinics of North America, 2009 Management of immune thrombocytopenia in pregnancy can be a complex and challenging task and may be complicated by fetal-neonatal thrombocytopenia. Although fetal intracranial hemorrhage is a rare complication of immune thrombocytopenia in pregnancy, invasive studies designed to determine the fetal platelet count before delivery are associated with ...
Keith R McCrae, Evi X Stavrou
exaly +3 more sources
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Immune Thrombocytopenia Treatment
New England Journal of Medicine, 2021Idiopathic thrombocytopenia (ITP) has a long history. In 1025, Avicenna described in the Canon of Medicine a patient with characteristics of ITP, which became known as “idiopathic thrombocytopenic ...
Paula H.B. Bolton-Maggs, James N. George
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Hospital Practice, 1983
The common denominator of this group of disorders is bleeding due to antibody-mediated platelet destruction. The variations in clinical manifestation--ranging from mild to fatal--reflect the diverse origins of the troublesome antibodies: transplacental, exogenous, and autogenous.
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The common denominator of this group of disorders is bleeding due to antibody-mediated platelet destruction. The variations in clinical manifestation--ranging from mild to fatal--reflect the diverse origins of the troublesome antibodies: transplacental, exogenous, and autogenous.
openaire +2 more sources
Pathophysiology of immune thrombocytopenia
Current Opinion in Hematology, 2018Purpose of review Immune thrombocytopenia (ITP) is a common autoimmune bleeding disorder with as of yet, no established clinical prognostic or diagnostic biomarkers. Patients frequently experience a markedly decreased quality of life and may be at risk for severe/fatal haemorrhage.
June, Li, Jade A, Sullivan, Heyu, Ni
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GESTATIONAL THROMBOCYTOPENIA AND IMMUNE THROMBOCYTOPENIAS IN PREGNANCY
Hematology/Oncology Clinics of North America, 2000Appropriate management of thrombocytopenia in the pregnant patient is important for the well-being of both mother and fetus. The healthy-appearing mother with mild thrombocytopenia may have either gestational benign thrombocytopenia, which does not produce fetal thrombocytopenia, or immune-mediated thrombocytopenia, which can produce fetal ...
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Immune thrombocytopenia in children
Journal of Pediatric Hematology/Oncology, 1981Idiopathic thrombocytopenic purpura in the adult has a clearly established autoimmune etiology; IgG antiplatelet antibody is demonstrable on the patient's platelets and is frequently present in the serum. Platelet IgG is correlated inversely with the platelet count.
M, Karpatkin, S, Karpatkin
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Other Immune Thrombocytopenias
Seminars in Hematology, 2007Immune thrombocytopenic purpura (ITP) can be classified as primary (known also as idiopathic thrombocytopenic purpura) or as secondary to an underlying condition such as a malignant or nonmalignant disorder. Commonly occurring conditions associated with secondary ITP include lymphoproliferative disorders (chronic lymphocytic leukemia [CLL], Hodgkin's ...
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