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The thalassemia syndromes are inherited disorders of hemoglobin synthesis associated with heterogeneous clinical manifestations ranging from barely detectable microcytosis to profound transfusion-dependent anemia associated with severe stigmata of hemolysis and ineffective erythropoiesis.
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About the Journal
Hematology/Oncology Clinics updates you on the latest trends in patient management, keeps you up to date on the newest advances, and provides a sound basis for choosing treatment options. Under the direction of an experienced guest editor, each issue focuses on a single topic in hematology and oncology, including hemostasis and thrombosis, molecular and cellular basis of hematology, coagulation disorders, and cancers—bone, gastrointestinal, head and neck, lymphomas, neuroendocrine, breast, renal cell, melanoma, and more. Hematology/Oncology Clinics of North America is published six times each year, in February, April, June, August, October, and December.