Hemoglobin, Sickle
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Subject Areas on Research
- Absence of Association Between Sickle Trait Hemoglobin and Placental Malaria Outcomes.
- Associated risk factors for silent cerebral infarcts in sickle cell anemia: low baseline hemoglobin, sex, and relative high systolic blood pressure.
- Cerebral infarction in sickle cell trait.
- Chronic transfusion practices for prevention of primary stroke in children with sickle cell anemia and abnormal TCD velocities.
- Controlled trial of transfusions for silent cerebral infarcts in sickle cell anemia.
- Correction of sickle cell disease in transgenic mouse models by gene therapy.
- Diagnosis and management of common bile duct stones in patients with sickle hemoglobinopathies.
- Effect of red blood cell variants on childhood malaria in Mali: a prospective cohort study.
- Effect of the beta 73 amino acid on the hydrophobicity, solubility, and the kinetics of polymerization of deoxyhemoglobin S.
- Effects of S-nitrosation on oxygen binding by normal and sickle cell hemoglobin.
- Functional properties of normal and sickle cell hemoglobins in polyethylene glycol 6000.
- Genetic polymorphisms associated with priapism in sickle cell disease.
- Genome-wide and fine-resolution association analysis of malaria in West Africa.
- Haemoglobinopathies and the clinical epidemiology of malaria: a systematic review and meta-analysis.
- Heme redox properties of S-nitrosated hemoglobin A0 and hemoglobin S: implications for interactions of nitric oxide with normal and sickle red blood cells.
- Hemoglobin C Trait Provides Protection From Clinical Falciparum Malaria in Malian Children.
- Hemoglobin C associated with protection from severe malaria in the Dogon of Mali, a West African population with a low prevalence of hemoglobin S.
- Hemoglobin sickle-Lepore: report of two siblings and review of the literature.
- Impaired vasodilation by red blood cells in sickle cell disease.
- Long-term management of splenic sequestration in children with sickle cell disease.
- MEK1/2 inhibitors reverse acute vascular occlusion in mouse models of sickle cell disease.
- Malaria parasites and red cell variants: when a house is not a home.
- Neurocognitive development of young children with sickle cell disease through three years of age.
- New insights provided by a comparison of impaired deformability with erythrocyte oxidative stress for sickle cell disease.
- Nucleation of microtubule assembly. Experimental kinetics, computer fitting of models, and observations on tubulin rings.
- Patent foramen ovale in adults with sickle cell disease and stroke.
- Pitfalls in newborn hemoglobinopathy screening: failure to detect beta(+)-thalassemia.
- Quantitative analysis of erythrocytes containing fetal hemoglobin (F cells) in children with sickle cell disease.
- Responses of normal and sickle cell hemoglobin to S-nitroscysteine: implications for therapeutic applications of NO in treatment of sickle cell disease.
- Sickle hemoglobin (HbS) allele and sickle cell disease: a HuGE review.
- Stable mixed hematopoietic chimerism after bone marrow transplantation for sickle cell anemia.
- The clinical manifestations of cerebral malaria among Nigerian children with the sickle cell trait.
- The clinical severity of hemoglobin S/Black (A γδβ)0 -thalassemia.
- The genomic analysis of erythrocyte microRNA expression in sickle cell diseases.
- The lung in sickle cell disease.
- Thermodynamic and kinetic aspects of assembly.
- Translocation of sickle cell erythrocyte microRNAs into Plasmodium falciparum inhibits parasite translation and contributes to malaria resistance.
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Keywords of People
- Shah, Nirmish Ramesh, Associate Professor of Medicine, School of Nursing