Results 111 to 120 of about 18,864 (254)
Erythrocytapheresis as a novel treatment option for adult patients with pyruvate kinase deficiency
Rawia F.G. Jensen +4 more
doaj +1 more source
ABSTRACT Background and Aims The polymerization of deoxygenated hemoglobin S, resulting from a genetic mutation in sickle cell disease (SCD), leads to damage in multiple organs, including renal, cardiopulmonary, and cerebrovascular systems. The liver is also commonly affected, resulting in “sickle cell liver disease,” which may lead to progressive ...
Josué Louokdom Simo +6 more
wiley +1 more source
Hemoglobinopathies: slicing the Gordian knot of Plasmodium falciparum malaria pathogenesis.
Plasmodium falciparum malaria kills over 500,000 children every year and has been a scourge of humans for millennia. Owing to the co-evolution of humans and P.
Rick M Fairhurst +7 more
core +1 more source
American Journal of Hematology, Volume 101, Issue 6, Page 1196-1200, June 2026.
Bo A. Wan +7 more
wiley +1 more source
Abstract Background The prevalence of iron deficiency with anemia and iron deficiency without anemia (IDWA) during pregnancy have not been summarized, and evidence of the direct association of IDWA with adverse perinatal outcomes (APO) are unknown.
Lucky O. Lawani +6 more
wiley +1 more source
Hemoglobinopathies and preimplantation diagnostics
Hemoglobinopathies constitute some of the most common inherited disorders worldwide. Manifestations are very severe, patient management is difficult and treatment is not easily accessible.
Mamas, T. +3 more
core
Hemoglobinopathies types and their peculiarities in India
Hemoglobinopathies, including thalassemias and sickle cell disorders are among the most prevalent inherited autosomal recessive blood disorders globally and pose significant public health challenges in India.
Ткаченко, Олена Вікторівна +2 more
core
Hemoglobinopathies, G6PD Deficiency, and Hereditary Elliptocytosis in Bahrain
The native population of Bahrain has a high prevalence of hemoglobinopathies and G6PD deficiency, probably as a result of past malarial endemism. We used the Biorad-Variant hemoglobin testing system for primary screening of hemoglobinopathies in 20,000 ...
Dash, Sumitra
core
Transcranial Doppler Ultrasound Velocity Measurements in Children With Sickle Cell Disease in Kenya
ABSTRACT Background Sickle cell disease (SCD) is the most common inherited haemoglobinopathy and poses a high public health burden in Sub‐Saharan Africa. Children with sickle cell anaemia are at a highrisk of ischemic stroke, and transcranial Doppler (TCD) ultrasonography helps identify those at highest risk for primary stroke prevention.
Catherine Mwalimu +9 more
wiley +1 more source

