Results 191 to 200 of about 41,059 (248)
Idiopathic thrombocytopenic purpura andgestational process (lecture)
, 2003 M Yu Sokolova, Markéta Sokolová
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The management of idiopathic thrombocytopenic purpura.
, 1959 Arthur A. Cooperberg
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Annals of the Rheumatic Diseases, 2020
Background Idiopathic thrombocytopenic purpura (ITP) may play a role in early-stage systemic lupus erythematosus (SLE). The incidence of SLE in patients with ITP and the potential relationship between them is still unclear.
F. Zhu +4 more
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Background Idiopathic thrombocytopenic purpura (ITP) may play a role in early-stage systemic lupus erythematosus (SLE). The incidence of SLE in patients with ITP and the potential relationship between them is still unclear.
F. Zhu +4 more
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First‐in‐patient study of hetrombopag in patients with chronic idiopathic thrombocytopenic purpura
Journal of Thrombosis and Haemostasis, 2020Idiopathic thrombocytopenic purpura (ITP) especially refractory and (or) relapsed ITP, is a serious and global health burden and its clinical treatment is far from being satisfied.
Zhenlei Wang +10 more
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Idiopathic thrombocytopenic purpura
The American Journal of Medicine, 1983Idiopathic thrombocytopenic purpura occurs at all ages, in acute and chronic forms. Children mainly have the acute form, which usually follows a recent viral illness, occurs equally in both sexes, and generally resolves within six months. Chronic idiopathic thrombocytopenic purpura occurs more often in adults, often has an insidious onset, and shows a ...
T R, Burns, A, Saleem
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Chronic idiopathic thrombocytopenic purpura.
BMJ, 1981CHRONIC idiopathic (or immune) thrombocytopenic purpura (ITP) is a syndrome characterized by persistent thrombocytopenia caused by a circulating antiplatelet factor that results in platelet destruction by the reticuloendothelial system. It seems likely that the antiplatelet factor in most patients is an IgG antibody directed toward a platelet ...
I G, Barrison, K, Jeyasingh, R, Jewkes
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Acute idiopathic thrombocytopenic purpura
Oral Surgery, Oral Medicine, Oral Pathology, 1984A 35-year-old man had hemorrhagic bullae of the buccal and sublingual mucosa as the first sign of acute idiopathic thrombocytopenic purpura. Twenty-four hours later the more typical cutaneous manifestations of petechiae of the lower extremities were present.
W D, James, C C, Guiry, W R, Grote
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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.
A, Ballin +8 more
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Idiopathic Thrombocytopenic Purpura
Postgraduate Medicine, 1962The acute form of ITP may be drug-induced or may follow infection or exposure to chemicals. The chronic form represents a self-perpetuating immunologic (auto-immune) disorder, at times associated with chronic lymphatic leukemia and other disorders. In some cases, it may be a prodrome of systemic lupus, to which it seems to be closely related.
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Idiopathic thrombocytopenic purpura
Current Paediatrics, 1995Idiopathic thrombocytopenic purpura in children usually a self limiting disorder. It may follow a viral infection or immunisation and is caused by an inappropriate response of the immune system. About 20-30% of children will fail to remit over six months (chronic idiopathic thrombocytopenic purpura).
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