Adding eltrombopag to immunosuppression: the importance of predicting outcome
André Tichelli+3 more
doaj +1 more source
Blood Transfusion Frequency and Indications in Yemeni Children with Sickle Cell Disease
Background. Blood transfusion is an essential component in the care of patients with sickle cell disease (SCD), but it might be associated with serious acute and delayed complications.
Abdul-Wahab M. Al-Saqladi+2 more
doaj +1 more source
Novel mutation in addition to functional TMPRSS6 gene polymorphisms originate an IRIDA-like phenotype in an African child [PDF]
Iron-refractory iron deficiency anemia (IRIDA) is a rare autosomal recessive anemia often unresponsive to oral iron intake and partially responsive to parenteral iron treatment. The disease originates from mutations in TMPRSS6 gene, encoding Matriptase 2,
Batalha, Sara+7 more
core
Earliest Porotic Hyperostosis on a 1.5-Million-year-old Hominin, olduvai gorge, Tanzania. [PDF]
Meat-eating was an important factor affecting early hominin brain expansion, social organization and geographic movement. Stone tool butchery marks on ungulate fossils in several African archaeological assemblages demonstrate a significant level of ...
Agness Gidna+17 more
core +5 more sources
Hypoxia-Inducible Factor Activators in Renal Anemia: Current Clinical Experience.
Prolyl hydroxylase domain oxygen sensors are dioxygenases that regulate the activity of hypoxia-inducible factor (HIF), which controls renal and hepatic erythropoietin production and coordinates erythropoiesis with iron metabolism.
Neil S. Sanghani, V. Haase
semanticscholar +1 more source
CORRELATION BETWEEN THE MEAN CORPUSCULAR VOLUME AND RETICULOCYTOSIS IN PHENYLHYDRAZINE ANEMIA IN SWINE [PDF]
F. Douglas Lawrason+3 more
openalex +1 more source
Objective. Sickle cell disease (SCD) is a disease that requires a significant degree of medical intervention, and family physicians are one potential provider of care for patients who do not have access to specialists.
Arch G. Mainous+5 more
doaj +1 more source
The Properties of Red Blood Cells from Patients Heterozygous for HbS and HbC (HbSC Genotype)
Sickle cell disease (SCD) is one of the commonest severe inherited disorders, but specific treatments are lacking and the pathophysiology remains unclear.
A. Hannemann+5 more
doaj +1 more source
Effect of Combined Oral Ferrotherapy with L-carnitine on Exercise Tolerance of Patients with Chronic Heart Failure with Reduced Ejection Fraction of Left Ventricle with Concomitant Iron Deficiency Anemia [PDF]
According to numerous studies, a high prevalence of iron deficiency (ID) with anaemic syndrome and its association with mortality during chronic heart failure (CHF) have been revealed.
Ivanov, V. (Valerii)+1 more
core +3 more sources
Fanconi anemia (FA) is a recessively inherited disease characterized by multiple symptoms including growth retardation, skeletal abnormalities, and bone marrow failure.
Petra van der Lelij+4 more
doaj +1 more source