Anemia, Sickle Cell Concept

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
• A sickle cell disease patient with dural venous sinus thrombosis: a case report and literature review  Academic Article
• A user guide to the American Society of Hematology clinical practice guidelines  Academic Article
• American Society of Hematology 2019 guidelines for sickle cell disease: cardiopulmonary and kidney disease  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
• Clinical phenotypes of three children with sickle cell disease caused by HbS /Sicilian (δβ) ⁰ ‐thalassemia deletion  Academic Article
• Coexisting Systemic Lupus Erythematosus and Sickle Cell Disease  Academic Article
• Combined preoperative plasma exchange and red blood cell exchange transfusion in a renal transplant patient with protein S deficiency and hemoglobin SC disease  Academic Article
• Cross-sectional prospective feasibility study of newborn screening for sickle cell anaemia and congenital hypothyroidism in Guyana  Academic Article
• Emotional distress among parent caregivers of adolescents with sickle cell disease: Association with patients and caregivers variables  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
• Inhibition of LSD1 by small molecule inhibitors stimulates fetal hemoglobin synthesis  Academic Article
• Ketamine administration for acute painful sickle cell crisis: A randomized controlled trial  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
• 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
• Pharmacologic induction of PGC ‐1α stimulates fetal haemoglobin gene expression  Academic Article
• Pharmacy hydroxyurea education materials for patients with sickle cell disease: An environmental scan and assessment of accuracy  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
• Splenic function: physiology and splenic hypofunction  Academic Article
• Study protocol for a randomized, blinded, controlled trial of ketamine for acute painful crisis of sickle cell disease  Academic Article
• Stuttering priapism in a patient with sickle cell trait treated with automated red cell exchange transfusion  Academic Article
• The Effect of Sickle Cell Anaemia on Adolescents and Their Growth and Development-Lessons from the Sickle Cell Anaemia Clinic  Academic Article
• The Intrauterine Diagnosis of Hemoglobin Disorders  Academic Article
• The Novel Hemoglobin-based Oxygen Carrier HRC 101 Improves Survival in Murine Sickle Cell Disease  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
• Utilising red cell antigen genotyping and serological phenotyping in sickle cell disease patients to risk‐stratify patients for alloimmunisation risk  Academic Article
• Variants of ZBTB7A (LRF) and its β-globin gene cluster binding motifs in sickle cell anemia  Academic Article