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Fetal Hemoglobin, Sickling, and Sickle Cell Disease
Advances in Pediatrics, 1990Increased numbers of F cells and large amounts of Hb F/F cell appear to produce clinical benefit in rare variants of sickle cell disease and probably in more commonly encountered patients. Fetal hemoglobin interferes with polymerization of Hb S in vitro, but laboratory studies carried out with homogeneous hemoglobin solutions are inadequate models of ...
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Hydroxyurea for sickle cell disease
2001Sickle cell disease is one of the most common inherited diseases world wide. It is associated with life long morbidity and a reduced life expectancy. Hydroxyurea, a chemotherapeutic drug taken by mouth, raises fetal haemoglobin and, as such, is expected to ameliorate some of the clinical problems of sickle cell disease.To assess the effects of ...
Ashley P Jones +2 more
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Cholangiopathy in sickle cell disease
Clinics and Research in Hepatology and Gastroenterology, 2023E, Vo Quang +3 more
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Acute Care Utilization and Rehospitalizations for Sickle Cell Disease
JAMA - Journal of the American Medical Association, 2010David C Brousseau +2 more
exaly
SICKLE CELL DISEASE AND PREGNANCY
Obstetrical & Gynecological Survey, 1957R H, BANNERMAN, J C, WHITE
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