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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 ...
Dec 6, 2005 ... ment, have altered the clinical spectrum of thalassemia, one of the world's ...
sored North American Thalassemia Clinical Research. Network ...
fi-thalassemia is increasing because of belier treatment and decreased births. A
countering influence is immigration of ethnic groups with a high prevalence of.
The authors have described the second case in the United States of chronic
hemolytic anemia resulting from the genetic factors for sicklemia and thalassemia
THALASSEMIA-HEMOGLOBIN. C DISEASE. IN WHITE. SIBLINGS. By Marion.
Erlandson,. M.D.,. Carl H. Smith,. M.D., and. Irving. Schulman,. M.D.. Department.
Dec 1, 2005 ... Severe thalassemia, based on observations of Italian children with characteristic
anemia and bone deformities, was first described in North ...
Two white sisters of Italian parentage in whom thalassemia-hemoglobin C
disease was found, have been presented. This is the third report of such cases