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American Journal of Hematology|April 1, 1989
Platelet survival and turnover: important factors in predicting response to splenectomy in immune thrombocytopenic purpuraR S Siegel, J L Rae, S Barth, et al.
Blood|June 1, 1980
Complement sensitivity of paroxysmal nocturnal hemoglobinuria bone marrow cellsJ Tumen, L B Kline, J W Fay, et al.
The New England Journal of Medicine|June 9, 1994
Mortality in sickle cell disease. Life expectancy and risk factors for early deathO S Platt, D J Brambilla, W F Rosse, et al.
The New England Journal of Medicine|July 4, 1991
Pain in sickle cell disease. Rates and risk factorsO S Platt, B D Thorington, D J Brambilla, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1988
Normal polymorphic variations and transcription of the decay accelerating factor gene in paroxysmal nocturnal hemoglobinuria cellsH A Stafford, M L Tykocinski, D M Lublin, et al.
Cancer|March 15, 1993
Treatment of myelodysplastic syndromes with daily oral idarubicin. A phase I-II studyB R Greenberg, R D Reynolds, C B Charron, et al.
Blood|March 15, 1992
Defective glycosylphosphatidylinositol anchor synthesis in paroxysmal nocturnal hemoglobinuria granulocytesJ F Mahoney, M Urakaze, S Hall, et al.
Blood|May 9, 2001
Efficient retrovirus-mediated PIG-A gene transfer and stable restoration of GPI-anchored protein expression in cells with the PNH phenotypeNishimura Ji, K L Phillips, R E Ware, et al.
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