Essential Thrombocythemia: Another “Heterogeneous Disease” Better Understood?
Author:
Affiliation:
1. From the Division of Hematologic Oncology, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, NY.
Publisher
American Society of Hematology
Subject
Cell Biology,Hematology,Immunology,Biochemistry
Link
http://ashpublications.org/blood/article-pdf/93/2/415/1650386/415.pdf
Reference12 articles.
1. A large proportion of patients with a diagnosis of essential thrombocythemia do not have a clonal disorder and may be at lower risk of thrombotic complications.;Harrison;Blood,1998
2. Incidence and risk factors for thrombotic complications in a historical cohort of 100 patients with essential thrombocythemia.;Cortelazzo;J Clin Oncol,1990
3. Treatment strategies in essential thrombocythemia. A critical appraisal of various experiences in different centers.;Barbui;Leuk Lymphoma,1996
4. Acute myeloid leukemia and myelodysplastic syndromes following essential thrombocythemia treated with hydroxyurea: High proportion of cases with 17p deletion.;Sterkers;Blood,1998
5. Clonality analysis of hematopoiesis in essential thrombocythemia: Advantages of studying T lymphocytes and platelets.;El-Kassar;Blood,1997
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