Results 261 to 270 of about 48,507 (298)
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Transient reversal of thrombocytopenia in idiopathic thrombocytopenic purpura by high-dose intravenous gamma globulin.

New England Journal of Medicine, 1982
Since recent observations indicate that treatment with high-dose intravenous polyvalent intact immunoglobulin leads to a rapid reversal of thrombocytopenia in the idiopathic thrombocytopenic purpura (ITP) of childhood, we decided to apply this treatment ...
J. Fehr, V. Hofmann, Urs Rappeler
semanticscholar   +1 more source

Idiopathic thrombocytopenic purpura and pregnancy

International Journal of Gynecology & Obstetrics, 1999
Ž . 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

Idiopathic Thrombocytopenic Purpura

JAMA: The Journal of the American Medical Association, 1975
To 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

Thrombokinetics in Idiopathic Thrombocytopenic Purpura*

British Journal of Haematology, 1970
Summary 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

Idiopathic Thrombocytopenic Purpura in Adults

Journal of Pediatric Hematology/Oncology, 2003
Immune 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

Infantile Idiopathic Thrombocytopenic Purpura

Pediatric Hematology and Oncology, 1990
Idiopathic 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

Chronic Idiopathic Thrombocytopenic Purpura

New England Journal of Medicine, 1994
Idiopathic 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

Idiopathic Thrombocytopenic Purpura in Pregnancy

Clinics in Perinatology, 1985
Idiopathic thrombocytopenic purpura (ITP) frequently occurs in young women, and is therefore encountered in pregnancy. Any woman with a history of ITP, regardless of her clinical status, has some risk of delivering a thrombocytopenic infant, since the antiplatelet antibodies cross the placenta. Methods for predicting which infants are at high risk, for
openaire   +3 more sources

Idiopathic thrombocytopenic purpura in the elderly

The American Journal of the Medical Sciences, 1978
Idiopathic thrombocytopenic purpura (ITP) was diagnosed in 22 patients above the age of 50 during a seven-year period. There was no female preponderance. Steroid therapy was effective, particularly in preventing hemorrhage and is considered to be the treatment of choice.
Charles E. Rath, George G. Shashaty
openaire   +3 more sources

Familial idiopathic thrombocytopenic purpura

The Journal of Pediatrics, 1963
The unusual occurrence of idiopathic thrombocytopenic purpura in 4 brothers is described. The purpura appeared in early infancy and continued for 1 to 3 years until controlled by splenectomy. The thrombocytopenic purpura was not associated with any other blood dyscrasia, drug, toxin, platelet antibodies, or maternal antibodies.
openaire   +3 more sources

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