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
- Association of wheeze with lung function decline in children 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
- 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
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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
- Desire for biological parenthood and patient counseling on the risk of infertility among adolescents and adults with hemoglobinopathies 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
- 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
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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
- 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
- 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
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Sickle cell disease in
S audiA rabia: the phenotype in adults with theA rab‐I ndian haplotype is not benign Journal Articles - Sickle cell disease: no longer a single gene disorder Journal Articles
- Some ethical and design challenges of screening programs and screening tests Journal Articles
- Splenic function: physiology and splenic hypofunction Journal Articles
- Study protocol for a randomized, blinded, controlled trial of ketamine for acute painful crisis of sickle cell disease 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
- 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