Zobrazeno 1 - 10
of 66
pro vyhledávání: '"Murray N. Silverstein"'
Publikováno v:
Blood. 95:2226-2233
In a 20-year period, 223 patients (median age, 64.8 years) with myelofibrosis with myeloid metaplasia (MMM) had therapeutic splenectomy at our institution. Primary indications for surgery were transfusion-dependent anemia (45.3%), symptomatic splenom
Autor:
Ayalew Tefferi, Murray N. Silverstein
Publikováno v:
Baillière's Clinical Haematology. 11:769-785
The clinical course in both polycythaemia vera (PV) and essential thrombocythaemia (ET) is characterized by significant thrombohaemorrhagic complications and variable risk of disease transformation into myeloid metaplasia with myelofibrosis or acute
Publikováno v:
British Journal of Haematology. 103:505-511
Twenty-three patients who had myelofibrosis with myeloid metaplasia (MMM) were treated at our institution with 50 courses of splenic irradiation (SI) for symptomatic splenomegaly. The median dose of radiation per course was 277.5 cGy, administered in
Publikováno v:
Seminars in Thrombosis and Hemostasis. 23:379-383
Anagrelide is an oral imidazoquinazoline agent with an anti-cyclic AMP phosphodiesterase activity and inhibits platelet aggregation in both humans and animals. In addition, it has in humans a species-specific platelet-lowering activity observed at do
Publikováno v:
Blood Reviews. 11:1-7
Among the chronic myeloproliferative disorders, polycythemia vera and essential thrombocythemia are unique because of their association with thrombohemorrhagic manifestations and their relatively indolent clinical course. Patients with essential thro
Publikováno v:
American Journal of Hematology. 46:325-328
Life-threatening portal hypertension (PHN) in patients with chronic myeloproliferative disorders may result from increased portal flow caused by marked splenomegaly or an increased resistance to portal flow from either a large vein thrombosis or an i
Publikováno v:
The American journal of medicine. 109(2)
Polycythemia vera and essential thrombocythemia pose specific management issues that distinguish them from other chronic myeloproliferative disorders. They are associated with a better prognosis, as well as a variable risk of thrombohemorrhagic compl
Publikováno v:
British journal of haematology. 99(2)
2-Chlorodeoxyadenosine (2-CdA) is a purine nucleoside analogue with therapeutic activity in low-grade lymphoproliferative disorders. In addition, 2-CdA has a potent myelosuppressive effect, and it has been shown to be toxic to malignant myeloid cells
Autor:
Robert M. Petitt, Lee A. Forstrom, Murray N. Silverstein, Jerzy S. Tarach, Lawrence A. Solberg, Ayalew Tefferi, Karl J. Oles
Publikováno v:
British journal of haematology. 99(1)
Anagrelide, an inhibitor of platelet aggregation, decreases the number of platelets in normal subjects and in patients with myeloproliferative disorders. We describe studies aimed at discovering the general mechanism(s) by which anagrelide acts. We e
Autor:
Ayalew Tefferi, Murray N. Silverstein
Publikováno v:
Leukemialymphoma. 22
Agnogenic myeloid metaplasia (AMM) carries the worst prognosis among the chronic myeloproliferative disorders. Substantial bone marrow fibrosis, extramedullary hematopoiesis, anemia and hepatosplenomegaly are the characteristic features of the diseas