Results 221 to 230 of about 23,927 (264)
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Familial essential thrombocythemia
The American Journal of Medicine, 1986Primary or essential thrombocythemia is rarely observed in childhood, and familial occurrence has been reported only once. In this study, essential thrombocythemia is documented in five members of both sexes from two to 62 years of age in three successive generations.
M E, Eyster +6 more
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Management of Essential Thrombocythemia
Critical Reviews in Oncology/Hematology, 19993. Risk stratification of patients with ET . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 258 3.1. Bleeding and thrombosis in ET . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 258 3.2. Risk factors for major bleeding . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 259 3.3. Risk factors for thrombosis. .
T, Barbui, G, Finazzi
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Familial Essential Thrombocyteemia
Pediatric Hematology and Oncology, 1990We report three siblings (2 F, 1 M) aged 9, 12, and 15 years with a thrombocytosis, above 650 X 10(9)/l for at least 18 months and a leukocyte alkaline phosphatase score below 37. The diagnosis of essential thrombocythemia was based upon the exclusion of a reactive thrombocytosis or another myeloproliferative disease.
Fernandez-Robles, E +4 more
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Hypertension Complicating Essential Thrombocythemia
The American Journal of the Medical Sciences, 1988Essential thrombocythemia (ET) is a myeloproliferative disorder characterized by marked thrombocytosis with associated hemorrhagic, thrombotic and embolic complications caused by platelet dysfunction. In this report we describe two cases of ET and moderate to severe hypertension associated with renal artery stenosis and renal microvascular lesions.
J S, Bruch, R S, Stein, J A, Oates
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The Journal for Nurse Practitioners, 2023
Ruth Madden Foreman, Richard Brzustowicz
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Ruth Madden Foreman, Richard Brzustowicz
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