Hydroxyurea promotes the reduction of spontaneous BFU-e to normal levels in SS and S/β thalassemic patients

Hemoglobin

Volumn 25, Issue 1, 2001, Pages 1-7

  Bincoletto, C ^a   Perlingeiro, R C R ^a   Saad, S T O ^a   Costa, F F ^a   Queiroz, M L S ^a  

^a UNIVERSITY OF CAMPINAS   (Brazil)

Author keywords

[No Author keywords available]

Indexed keywords

ERYTHROPOIETIN; HEMOGLOBIN A2; HEMOGLOBIN F; HYDROXYUREA;

ARTICLE; BETA THALASSEMIA; BURST FORMING UNIT E; CELL CULTURE; CELL PROLIFERATION; CLINICAL ARTICLE; CONTROLLED STUDY; DRUG EFFECT; HEMOGLOBIN DETERMINATION; HUMAN; HUMAN CELL; MONONUCLEAR CELL; SICKLE CELL ANEMIA;

ANEMIA, SICKLE CELL; ANTISICKLING AGENTS; BETA-THALASSEMIA; BLOOD CELL COUNT; CELL DIFFERENTIATION; CELL DIVISION; CELLS, CULTURED; CULTURE MEDIA, CONDITIONED; ERYTHROID PROGENITOR CELLS; ERYTHROPOIETIN; HETEROZYGOTE; HUMANS; HYDROXYUREA; SICKLE CELL TRAIT;

EID: 0035096732     PISSN: 03630269     EISSN: None     Source Type: Journal    
DOI: 10.1081/HEM-100103064     Document Type: Article

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