Results 181 to 190 of about 17,830 (205)
Some of the next articles are maybe not open access.
An idiopathic thrombocytopenic purpura with polyneuropathy
Immunologic Research, 2016Concurrent association of idiopathic thrombocytopenic purpura (ITP) and peripheral neuropathy is a rare condition. There are only few case reports published concerning peripheral neuropathy with ITP. One of the etiopathogenetic mechanisms proposed is intraneural hemorrhage, but the pathogenesis is not fully understood.
Paula David+3 more
openaire +3 more sources
Myelofibrosis and idiopathic thrombocytopenic purpura
Annals of Hematology, 1997A case of idiopathic myelofibrosis (IMF) with concomitant autoimmune thrombocytopenic purpura (AITP) is reported. The literature on platelet antibodies in IMF is reviewed.
E. F. M. Posthuma+3 more
openaire +3 more sources
Idiopathic thrombocytopenic purpura in lymphoma
Cancer, 1976Five patients with idiopathic thrombocytopenic purpura (ITP) associated with malignant lymphoma are presented, and twelve other cases reported in the literature are reviewed. Thirteen patients (76%) had Hodgkin's disease; two had diffuse histiocytic, one, diffuse mixed lymphoma.
Kyle Fink, Kyle Fink, Hamid Al-Mondhiry
openaire +3 more sources
Idiopathic Thrombocytopenic Purpura in Adults
Journal of Pediatric Hematology/Oncology, 2003Immune thrombocytopenic purpura (ITP) is an organ-specific autoimmune disorder in which platelets opsonized by antiplatelet antibodies are destroyed by the reticuloendothelial system. As a result the peripheral blood platelet count is low; if sufficiently severe, it may lead to bruising and mucocutaneous bleeding.
Drew Provan, Adrian C. Newland
openaire +3 more sources
Idiopathic Thrombocytopenic Purpura
2019Atopic symptoms and early-onset eczema are frequent findings in patients with Wiskott-Aldrich ...
Marianna Janoudaki+4 more
openaire +2 more sources
Thrombokinetics in Idiopathic Thrombocytopenic Purpura*
British Journal of Haematology, 1970Summary Measurements of platelet production in 16 patients with idiopathic thrombocytopenic purpura (ITP) demonstrate that megakaryocytopoiesis (total thrombopoiesis) and platelet turnover (effective thrombopoiesis) are increased in parallel to as much as 8 times normal. The marrow megakaryocytes show changes characteristic of stimulated thrombopoiesis.
openaire +3 more sources
Infantile Idiopathic Thrombocytopenic Purpura
Pediatric Hematology and Oncology, 1990Idiopathic thrombocytopenic purpura (ITP) in childhood is a benign disease, as only 10% to 20% of the patients have a chronic course. A retrospective study of 57 ITP patients ranging in age from four months to two years revealed that 30% of them proceeded to chronicity.
Moshe Nussinovitch+8 more
openaire +3 more sources
Idiopathic Thrombocytopenic Purpura
JAMA: The Journal of the American Medical Association, 1975To the Editor.— The distinction between the chronic and self-limited types of idiopathic thrombocytopenic purpura (ITP) was first drawn in 1951 on the basis of a study of 89 cases of ITP in the presteroid days. 1 Three points made in this review are worth reemphasizing at this time: (1) In self-limited ITP, severe thrombocytopenia may persist for as
openaire +2 more sources
Idiopathic thrombocytopenic purpura and pregnancy
International Journal of Gynecology & Obstetrics, 1999Ž . Idiopathic thrombocytopenic purpura ITP is a common disease of young women and its management during pregnancy is a clinical problem often w x faced by physicians 1 . Treatment is required for women with platelet counts -10=10rl and women with platelet counts 10]30=10rl who are in the second or third trimester or are bleedw x ing 2 .
D.M Paternoster+2 more
openaire +3 more sources
Chronic Idiopathic Thrombocytopenic Purpura
New England Journal of Medicine, 1994Idiopathic thrombocytopenic purpura (ITP), also referred to as primary immune thrombocytopenic purpura, is defined by a low platelet count, normal bone marrow, and the absence of other causes of th...
Gary E. Raskob+2 more
openaire +3 more sources