Hemoglobinopathies in South Gujarat population and incidence of anemia in them
SnehalataC Gupte+3 more
openalex +2 more sources
Hemoglobin Variants as Targets for Stabilizing Drugs. [PDF]
Žoldáková M+3 more
europepmc +1 more source
Gene Therapy for β-Hemoglobinopathies.
M. Cavazzana, C. Antoniani, A. Miccio
semanticscholar +1 more source
Genetic Modifiers of Hemoglobin Expression from a Clinical Perspective in Hemoglobinopathy Patients with Beta Thalassemia and Sickle Cell Disease. [PDF]
Diamantidis MD+5 more
europepmc +1 more source
High-Resolution HbA1cSeparation and Hemoglobinopathy Detection With Capillary Electrophoresis
Eloísa Urrechaga
openalex +1 more source
Clinical Complications and Healthcare Resource Utilization Associated with Conventional Management of Sickle Cell Disease with Recurrent Vaso-occlusive Crises and Transfusion-Dependent β-Thalassemia in Germany. [PDF]
Udeze C+10 more
europepmc +1 more source
Synthetic review on the different anthropological aspects of hemoglobinopathies in Tunisia
AH Khelil+3 more
openalex +2 more sources
Drugs Repurposing of Molecules Modulating Human Delta Globin Gene Expression via a Model of Transgenic Foetal Liver Cells: Implications for Beta-Hemoglobinopathy Therapeutics. [PDF]
Simbula M+7 more
europepmc +1 more source
Myopericarditis and Pericardial Effusion as the Initial Presentation of Systemic Lupus Erythematosus in a Patient with Sickle Cell Trait: A Case Report. [PDF]
Rojas-Cadena M+5 more
europepmc +1 more source