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A patient with familial thalassemia who developed a myeloproliferative disorder
with bidirectional involvement has been studied. It is suggested that because of ...
Abstract. A hemoglobin level of over 10 gm per 100 ml has been maintained by
transfusion in six children with thalassemia major. Chelating agents have been ...
Abstract. Two white sisters of Italian parentage in whom thalassemia-hemoglobin
C disease was found, have been presented. This is the third report of such ...
6 Dec 2005 ... ment, have altered the clinical spectrum of thalassemia, one of the world's ...
sored North American Thalassemia Clinical Research. Network ...
THALASSEMIA-HEMOGLOBIN. C DISEASE. IN WHITE. SIBLINGS. By Marion.
Erlandson,. M.D.,. Carl H. Smith,. M.D., and. Irving. Schulman,. M.D.. Department.
fi-thalassemia is increasing because of belier treatment and decreased births. A
countering influence is immigration of ethnic groups with a high prevalence of.