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Effects of co‐existing α‐thalassaemia in sickle cell disease on hydroxycarbamide therapy and circulating nucleic acids
Author(s) -
Vasavda Nisha,
Woodley Claire,
Allman Marlene,
Drašar Emma,
Awogbade Moji,
Howard Jo,
Thein Swee L.
Publication year - 2012
Publication title -
british journal of haematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.907
H-Index - 186
eISSN - 1365-2141
pISSN - 0007-1048
DOI - 10.1111/j.1365-2141.2011.08937.x
Subject(s) - hydroxycarbamide , medicine , fetal hemoglobin , acute chest syndrome , mean corpuscular volume , vaso occlusive crisis , haemolysis , hemoglobinopathy , disease , sickle cell anemia , gastroenterology , pediatrics , hematocrit , immunology , fetus , pregnancy , genetics , biology