STUDIES IN SICKLE CELL ANEMIA (SCA): PRELIMINARY OBSERVATION ON GASTROINTESTINAL DIGESTION AND ABSORPITON [PDF]
Fariborz Rahbar+2 more
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646 FETAL AND NEONATAL CORRELATES OF SICKLE CELL ANEMIA [PDF]
Howard A. Pearson+3 more
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Failure of the alpha-thalassemia gene to decrease the severity of sickle cell anemia [PDF]
C Natta
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Iron deficiency, still a rarity in children with sickle cell anemia in Ile-Ife, Nigeria
In this study, children with sickle cell anemia were evaluated for iron deficiency. Serum ferritin and free erythrocyte protoporphyrin free erythrocyte protoporphyrin (FEP) levels, mean corpuscular volume mean corpuscular volume (MCV) and mean ...
Olufunke Odunlade+3 more
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Quantitation of three types of gamma chain of HbF by high pressure liquid chromatography; application of this method to the HbF of patients with sickle cell anemia or the S-HPFH condition [PDF]
T. H. J. Huisman+6 more
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5-Azacytidine increases HbF production and reduces anemia in sickle cell disease: dose-response analysis of subcutaneous and oral dosage regimens [PDF]
GJ Dover+4 more
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Failure of desmopressin to lower serum sodium or prevent crisis in patients with sickle cell anemia [PDF]
Samuel Charache, WG Walker
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HEART DISEASE IN THALASSEMIA HETEROZYGOTES WITH SICKLE CELL ANEMIA [PDF]
Wesley Covitz+6 more
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Background: Secondary hemophagocytic lymphohistiocytosis (HLH) is a potentially fatal condition commonly triggered by infections. HLH secondary to hepatitis E or hepatitis A and E coinfection has been scarcely reported.
Govind Choudhary+2 more
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