Results 181 to 190 of about 156,843 (219)
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Idiopathic Thrombocytopenic Purpura in Children

The Nurse Practitioner, 1987
Idiopathic thrombocytopenic purpura is a disorder characterized by antibody-mediated platelet destruction. Other than thrombocytopenia and its consequences, the physical and laboratory examination of the child with ITP is normal. The prognosis in children is excellent; 90 percent will recover spontaneously within one year.
G A, Thomas, R T, O'Brien
openaire   +2 more sources

Idiopathic Thrombocytopenic Purpura in Children

Seminars in Thrombosis and Hemostasis, 2008
ITP in childhood is most often of the acute, self-limited variety, with spontaneous recovery occurring within a matter of days or weeks. In many of these children, acute thrombopenic purpura follows in the wake of a viral infection. While the pathogenesis is not entirely clear, it seem probable that the platelet membrane is altered by virus or by ...
J M, Lusher, R, Iyer
openaire   +2 more sources

Myelofibrosis and idiopathic thrombocytopenic purpura

Annals of Hematology, 1997
A case of idiopathic myelofibrosis (IMF) with concomitant autoimmune thrombocytopenic purpura (AITP) is reported. The literature on platelet antibodies in IMF is reviewed.
M A, Seelen   +3 more
openaire   +2 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.
A, Ballin   +8 more
openaire   +2 more sources

Idiopathic Thrombocytopenic Purpura

Archives of Internal Medicine, 1961
Until recent years splenectomy had been generally considered the treatment of choice in idiopathic thrombocytopenic purpura (ITP). 1 It has become clear, however, that spontaneous remissions occur in most patients having the acute form of the disease, 2 and with the advent of adrenal steroids and improved methods of transfusing platelets, most writers ...
W L, BUNTING, J M, KIELY, D C, CAMPBELL
openaire   +2 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...
J N, George, M A, el-Harake, G E, Raskob
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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.
G G, Shashaty, C E, Rath
openaire   +2 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   +2 more sources

Idiopathic Thrombocytopenic Purpura

Pediatrics In Review, 2000
Y W, Chu, J, Korb, K M, Sakamoto
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Epidemiology of the idiopathic inflammatory myopathies

Nature Reviews Rheumatology, 2023
Hector Chinoy   +2 more
exaly  

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