subject area of
- A 19-year-old woman with sickle cell disease and pain Academic Article
- A Comprehensive, Ethnically Diverse Library of Sickle Cell Disease-Specific Induced Pluripotent Stem Cells Academic Article
- A Novel Sickle Hemoglobin: Hemoglobin S-South End Academic Article
- A Novel Sickling Hemoglobinopathy Academic Article
- A candidate transacting modulator of fetal hemoglobin gene expression in the Arab-Indian haplotype of sickle cell anemia Academic Article
- A functional promoter polymorphism of the δ-globin gene is a specific marker of the Arab-Indian haplotype Academic Article
- A monocyte-TNF-endothelial activation axis in sickle transgenic mice: Therapeutic benefit from TNF blockade Academic Article
- A phased SNP-based classification of sickle cell anemia HBB haplotypes Academic Article
- Association of wheeze with lung function decline in children with sickle cell disease Academic Article
- Automated local maximum-intensity projection with three-dimensional vessel tracking Academic Article
- BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia Academic Article
- BCL11A is a major HbF quantitative trait locus in three different populations with β-hemoglobinopathies Academic Article
- Clinical analysis of mortality in hospitalized Zambian children with sickle cell anaemia. Academic Article
- Coexisting Systemic Lupus Erythematosus and Sickle Cell Disease Academic Article
- Comparison of responses evoked by mild indirect cooling and by sound in the forearm vasculature in patients with homozygous sickle cell disease and in normal subjects Academic Article
- Day-care management of sickle cell painful crisis in Jamaica: a model applicable elsewhere? Academic Article
- Family Practice Grand Rounds. Care of a troubled family and their child with sickle cell anemia. Academic Article
- Fanconi’s Anemia Effect or Sickle Cell Anemia Effect: That is the Question Academic Article
- Fetal haemoglobin levels and haematological characteristics of compound heterozygotes for haemoglobin S and deletional hereditary persistence of fetal haemoglobin Academic Article
- Fetal hemoglobin in sickle cell anemia Academic Article
- Fetal hemoglobin in sickle cell anemia: Genetic studies of the Arab-Indian haplotype Academic Article
- Fetal hemoglobin in sickle cell anemia: Molecular characterization of the unusually high fetal hemoglobin phenotype in African Americans Academic Article
- Fetal hemoglobin in sickle cell anemia: Saudi patients from the Southwestern province have similar HBB haplotypes but higher HbF levels than African Americans Academic Article
- Fetal hemoglobin in sickle cell anemia: a glass half full? Academic Article
- Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5′ olfactory receptor gene cluster Academic Article
- Genetic studies of fetal hemoglobin in the Arab-Indian haplotype sickle cell-β0thalassemia Academic Article
- Hb S/ +-thalassemia due to Hb sickle and a novel deletion of DNase I hypersensitive sites HS3 and HS4 of the locus control region Academic Article
- Hemoglobin SE Disease in Maine, and Severe Thalassemia in New Hampshire Academic Article
- Homozygosity for a haplotype in theHBG2-OR51B4region is exclusive to Arab-Indian haplotype sickle cell anemia Academic Article
- Longitudinal Decline in Lung Volume in a Population of Children with Sickle Cell Disease Academic Article
- Massive splenic infarction in an adolescent with hemoglobin S-HPFH Academic Article
- Neurological PRESentations in Sickle Cell PatientsAre Not Always Stroke: A Review of Posterior Reversible Encephalopathy Syndrome in Sickle Cell Disease Academic Article
- Normalized Transcranial Doppler Velocities, Stroke Prevention and Improved Pulmonary Function after Stem Cell Transplantation in Children with Sickle Cell Anemia Academic Article
- Optimal Manual Exchange Transfusion Protocol for Sickle Cell Disease: A Retrospective Comparison of Two Comprehensive Care Centers in the United Kingdom and Canada Academic Article
- Plasma factor VII and thrombin–antithrombin III levels indicate increased tissue factor activity in sickle cell patients Academic Article
- Prenatal Diagnosis of Hemoglobinopathies in Ontario, Canada Academic Article
- Recurrent acute splenic sequestration crisis due to interacting genetic defects: hemoglobin SC disease and hereditary spherocytosis. Academic Article
- Sickle Cell Traits in Canada Academic Article
- Sickle cell disease caused by Hb S/Québec-CHORI: Treatment with hydroxyurea and response Academic Article
- Sickle cell disease caused by heterozygosity for Hb S and novel LCR deletion: Report of two patients Academic Article
- Sickle cell disease due to compound heterozygosity for Hb S and a novel 7.7-kb ?-globin gene deletion Academic Article
- Sickle cell disease in Saudi Arabia: the phenotype in adults with the Arab-Indian haplotype is not benign Academic Article
- Sickle cell disease: no longer a single gene disorder Academic Article
- Some ethical and design challenges of screening programs and screening tests Academic Article
- The Intrauterine Diagnosis of Hemoglobin Disorders Academic Article
- The association of HBG2 , BCL11A, and HMIP polymorphisms with fetal hemoglobin and clinical phenotype in Iraqi Kurds with sickle cell disease Academic Article
- The clinical severity of hemoglobin S/Black (A γδβ)0 -thalassemia Academic Article
- The genetics of hemoglobin A2regulation in sickle cell anemia Academic Article
- The quality of information about sickle cell disease on the Internet for youth Academic Article
- Tonsillectomy and Adenoidectomy For Obstructive Sleep Apnea in Sickle Cell Anemia Academic Article
- Update on the use of hydroxyurea therapy in sickle cell disease Academic Article
- Variants of ZBTB7A (LRF) and its β-globin gene cluster binding motifs in sickle cell anemia Academic Article