Anemia, Sickle Cell Concept

subject area of

• 50 Years Ago in The Journal of Pediatrics  Journal Articles
• A 19-year-old woman with sickle cell disease and pain  Journal Articles
• A Comprehensive, Ethnically Diverse Library of Sickle Cell Disease-Specific Induced Pluripotent Stem Cells  Journal Articles
• A Novel Sickle Hemoglobin: Hemoglobin S-South End  Journal Articles
• A Novel Sickling Hemoglobinopathy  Journal Articles
• A candidate transacting modulator of fetal hemoglobin gene expression in the Arab—Indian haplotype of sickle cell anemia  Journal Articles
• A functional promoter polymorphism of the δ‐globin gene is a specific marker of the Arab‐Indian haplotype  Journal Articles
• A phased SNP-based classification of sickle cell anemia HBB haplotypes  Journal Articles
• A sickle cell disease patient with dural venous sinus thrombosis: a case report and literature review  Journal Articles
• A user guide to the American Society of Hematology clinical practice guidelines  Journal Articles
• American Society of Hematology 2019 guidelines for sickle cell disease: cardiopulmonary and kidney disease  Journal Articles
• American Society of Hematology 2020 guidelines for sickle cell disease: transfusion support  Journal Articles
• Association of wheeze with lung function decline in children with sickle cell disease  Journal Articles
• Attitudes, Beliefs, and Intention to Receive a COVID-19 Vaccine for Pediatric Patients With Sickle Cell Disease.  Journal Articles
• Automated local maximum‐intensity projection with three‐dimensional vessel tracking  Journal Articles
• BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia  Journal Articles
• BCL11A is a major HbF quantitative trait locus in three different populations with β-hemoglobinopathies  Journal Articles
• BCL2L1 is associated with γ-globin gene expression  Journal Articles
• CARE OF A TROUBLED FAMILY AND THEIR CHILD WITH SICKLE-CELL-ANEMIA  Journal Articles
• Clinical analysis of mortality in hospitalized Zambian children with sickle cell anaemia.  Journal Articles
• Clinical phenotypes of three children with sickle cell disease caused by HbS/Sicilian (δβ)⁰‐thalassemia deletion  Journal Articles
• Coexisting Systemic Lupus Erythematosus and Sickle Cell Disease  Journal Articles
• Combined preoperative plasma exchange and red blood cell exchange transfusion in a renal transplant patient with protein S deficiency and hemoglobin SC disease  Journal Articles
• Cord gas parameters in infants born to women with sickle cell disease: a retrospective matched cohort study  Journal Articles
• Cross-sectional prospective feasibility study of newborn screening for sickle cell anaemia and congenital hypothyroidism in Guyana  Journal Articles
• Emotional distress among parent caregivers of adolescents with sickle cell disease: Association with patients and caregivers variables  Journal Articles
• Estimated mortality rates of individuals with sickle cell disease in Brazil: real-world evidence  Journal Articles
• Family Practice Grand Rounds. Care of a troubled family and their child with sickle cell anemia.  Journal Articles
• Fanconi’s Anemia Effect or Sickle Cell Anemia Effect: That is the Question  Journal Articles
• Fetal haemoglobin levels and haematological characteristics of compound heterozygotes for haemoglobin S and deletional hereditary persistence of fetal haemoglobin  Journal Articles
• Fetal hemoglobin in sickle cell anemia  Journal Articles
• Fetal hemoglobin in sickle cell anemia: Genetic studies of the Arab-Indian haplotype  Journal Articles
• Fetal hemoglobin in sickle cell anemia: Molecular characterization of the unusually high fetal hemoglobin phenotype in African Americans  Journal Articles
• Fetal hemoglobin in sickle cell anemia: Saudi patients from the Southwestern province have similar HBB haplotypes but higher HbF levels than African Americans  Journal Articles
• Fetal hemoglobin in sickle cell anemia: a glass half full?  Journal Articles
• Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5′ olfactory receptor gene cluster  Journal Articles
• Genetic studies of fetal hemoglobin in the Arab‐Indian haplotype sickle cell‐β⁰ thalassemia  Journal Articles
• Hb S/ +-thalassemia due to Hb sickle and a novel deletion of DNase I hypersensitive sites HS3 and HS4 of the   locus control region  Journal Articles
• Hemoglobin SE Disease in Maine, and Severe Thalassemia in New Hampshire  Journal Articles
• Homozygosity for a haplotype in the HBG2‐OR51B4 region is exclusive to Arab‐Indian haplotype sickle cell anemia  Journal Articles
• Hydroxyurea effectiveness in children and adolescents with sickle cell anemia: A large retrospective, population-based cohort.  Journal Articles
• Impact of transcranial Doppler screening on stroke prevention in children and adolescents with sickle cell disease: A systematic review and meta-analysis.  Journal Articles
• Inhibition of LSD1 by small molecule inhibitors stimulates fetal hemoglobin synthesis  Journal Articles
• Ketamine administration for acute painful sickle cell crisis: A randomized controlled trial  Journal Articles
• Longitudinal Decline in Lung Volume in a Population of Children with Sickle Cell Disease  Journal Articles
• Massive splenic infarction in an adolescent with hemoglobin S‐HPFH  Journal Articles
• Neurological PRESentations in Sickle Cell Patients Are Not Always Stroke: A Review of Posterior Reversible Encephalopathy Syndrome in Sickle Cell Disease  Journal Articles
• Optimal Manual Exchange Transfusion Protocol for Sickle Cell Disease: A Retrospective Comparison of Two Comprehensive Care Centers in the United Kingdom and Canada  Journal Articles
• Pharmacologic induction of PGC‐1α stimulates fetal haemoglobin gene expression  Journal Articles
• Pharmacy hydroxyurea education materials for patients with sickle cell disease: An environmental scan and assessment of accuracy  Journal Articles
• Placental histopathology in sickle cell disease: A descriptive and hypothesis-generating study  Journal Articles
• Plasma factor VII and thrombin–antithrombin III levels indicate increased tissue factor activity in sickle cell patients  Journal Articles
• Point-of-care diagnostic test accuracy in children and adolescents with sickle cell disease: A systematic review and meta-analysis.  Journal Articles
• Prenatal Diagnosis of Hemoglobinopathies in Ontario, Canada  Journal Articles
• Prophylactic transfusion for pregnant women with sickle cell disease: a systematic review and meta-analysis  Journal Articles
• Protocol for a multicentric, double-blind, randomised controlled trial of hyperbaric oxygen therapy (HBOT) versus sham for treating vaso-occlusive crisis (VOC) in sickle cell disease (SCD) in patients aged 8 years or older (HBOT-SCD study).  Journal Articles
• Recurrent acute splenic sequestration crisis due to interacting genetic defects: hemoglobin SC disease and hereditary spherocytosis  Journal Articles
• Sickle Cell Traits in Canada  Journal Articles
• Sickle cell disease caused by Hb S/Québec‐CHORI: Treatment with hydroxyurea and response  Journal Articles
• Sickle cell disease caused by heterozygosity for Hb S and novel LCR deletion: Report of two patients  Journal Articles
• Sickle cell disease due to compound heterozygosity for Hb S and a novel 7.7‐kb β‐globin gene deletion  Journal Articles
• Sickle cell disease in Saudi Arabia: the phenotype in adults with the Arab‐Indian haplotype is not benign  Journal Articles
• Sickle cell disease: no longer a single gene disorder  Journal Articles
• Sickle cell trait does not cause "sickle cell crisis" leading to exertion-related death: a systematic review.  Journal Articles
• Some ethical and design challenges of screening programs and screening tests  Journal Articles
• Splenic function: physiology and splenic hypofunction  Journal Articles
• Splice Acceptor Mutation [ HBB :c.93-2A > T] in a Patient with Hb S/β ⁰ -Thalassemia  Journal Articles
• Stuttering priapism in a patient with sickle cell trait treated with automated red cell exchange transfusion  Journal Articles
• The Effect of Sickle Cell Anaemia on Adolescents and Their Growth and Development-Lessons from the Sickle Cell Anaemia Clinic  Journal Articles
• The Intrauterine Diagnosis of Hemoglobin Disorders  Journal Articles
• The association of HBG2, BCL11A, and HMIP polymorphisms with fetal hemoglobin and clinical phenotype in Iraqi Kurds with sickle cell disease  Journal Articles
• The clinical severity of hemoglobin S/Black (^Aγδβ)⁰‐thalassemia  Journal Articles
• The genetics of hemoglobin A₂ regulation in sickle cell anemia  Journal Articles
• The quality of information about sickle cell disease on the Internet for youth  Journal Articles
• Tonsillectomy and Adenoidectomy For Obstructive Sleep Apnea in Sickle Cell Anemia  Journal Articles
• Trends and hospital practice variation for analgesia for children with sickle cell disease with vaso-occlusive pain episodes: An 11-year analysis.  Journal Articles
• Update on the use of hydroxyurea therapy in sickle cell disease  Journal Articles
• Utilising red cell antigen genotyping and serological phenotyping in sickle cell disease patients to risk‐stratify patients for alloimmunisation risk  Journal Articles
• Variants of ZBTB7A (LRF) and its β-globin gene cluster binding motifs in sickle cell anemia  Journal Articles