Results 1 to 10 of about 1,271,889 (407)

Adding eltrombopag to immunosuppression: the importance of predicting outcome

open access: yesHaematologica, 2021
André Tichelli   +3 more
doaj   +1 more source

Blood Transfusion Frequency and Indications in Yemeni Children with Sickle Cell Disease

open access: yesAnemia, 2020
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]

open access: yes, 2019
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]

open access: yes, 2012
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.

open access: yesAdvances in Chronic Kidney Disease, 2019
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

Attitudes toward Management of Sickle Cell Disease and Its Complications: A National Survey of Academic Family Physicians

open access: yesAnemia, 2015
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)

open access: yesAnemia, 2011
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]

open access: yes, 2019
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

Diagnostic Overlap between Fanconi Anemia and the Cohesinopathies: Roberts Syndrome and Warsaw Breakage Syndrome

open access: yesAnemia, 2010
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

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