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Showing 1-20 of 2,414 results
  1. Knowledge and attitude towards sickle cell anemia among care givers of paediatric sickle cell patients at a tertiary hospital in Eastern Uganda: a cross sectional study

    Objective

    To explore the knowledge and attitude towards sickle cell disease (SCD) among care givers of paediatric sickle cell patients at Mbale...

    Christine H Namugerwa, Yahaya Gavamukulya, Banson John Barugahare in BMC Research Notes
    Article Open access 27 November 2023
  2. Detection of Transversions and Transitions in HBG2 Cis-Elements Associated with Sickle Cell Allele in Ghanaians

    Short tandem repeats located 5ʹ prime to the β-globin gene, have been observed to be in linkage disequilibrium with the HbS allele, and thought to...

    G. K. Ababio, I. Ekem, ... I. K. Quaye in Biochemical Genetics
    Article 03 July 2023
  3. Genetic counseling in sickle cell disease: Insights from the Indian tribal population

    Sickle cell disease (SCD) is an inherited disorder of hemoglobin. With an overall prevalence of 4.3%, India is the second-largest hub of SCD after...

    Pooja Aggarwal, Deepa Bhat in Journal of Community Genetics
    Article 04 August 2023
  4. Characterizing Intracranial Hemodynamics in Sickle Cell Anemia: Impact of Patient-Specific Viscosity

    Purpose

    Pediatric and adult patients with sickle cell anemia (SCA) are at increased risk of stroke and cerebrovascular accident. In the general adult...

    Sara B. Keller, Jacob M. Bumpus, ... Amanda K. W. Buck in Cardiovascular Engineering and Technology
    Article 20 July 2021
  5. Endline assessment of knowledge about sickle cell disease among the tribal community of Chhotaudepur district of Gujarat

    Sickle cell disease (SCD) is a significant public health concern in India, with one of the highest disability burdens worldwide. For the success of...

    Shaily B. Surti, Ankita Parmar, ... Shubhangi Patel in Journal of Community Genetics
    Article 09 February 2024
  6. Fetal hemoglobin-boosting haplotypes of BCL11A gene and HBS1L-MYB intergenic region in the prediction of clinical and hematological outcomes in a cohort of children with sickle cell anemia

    Single nucleotide polymorphisms (SNPs) of BCL11A gene and HBS1L-MYB intergenic region (named HMIP-2) affect both fetal hemoglobin (HbF) concentration...

    Rahyssa Rodrigues Sales, Bárbara Lisboa Nogueira, ... Marcelo Rizzatti Luizon in Journal of Human Genetics
    Article 27 September 2022
  7. Sickle Cell Gene

    Sickle cell gene is the signature of distribution of Plasmodium falciparum caused malaria throughout the world. Malaria parasite has imposed strong...
    Chapter 2021
  8. Sickle-cell anemia gene therapy

    Ornob Alam in Nature Genetics
    Article 06 August 2021
  9. Targeting Genetic Modifiers of HBG Gene Expression in Sickle Cell Disease: The miRNA Option

    Sickle cell disease (SCD) is one of the most common inherited hemoglobinopathy disorders that affects millions of people worldwide. Reactivation of...

    Athena Starlard-Davenport, Qingqing Gu, Betty S. Pace in Molecular Diagnosis & Therapy
    Article Open access 12 May 2022
  10. Diagnosis support of sickle cell anemia by classifying red blood cell shape in peripheral blood images

    Red blood cell (RBC) deformation is the consequence of several diseases, including sickle cell anemia, which causes recurring episodes of pain and...

    Wilkie Delgado-Font, Miriela Escobedo-Nicot, ... Arnau Mir in Medical & Biological Engineering & Computing
    Article 28 March 2020
  11. Translating research to usual care of children with sickle cell disease in Northern Nigeria: lessons learned from the SPRING Trial Team

    Objectives

    Evidence-based practice for stroke prevention in high-income countries involves screening for abnormal transcranial Doppler (TCD) velocity...

    Halima Bello-Manga, Lawal Haliru, ... Allison A. King in BMC Research Notes
    Article Open access 04 January 2022
  12. A phase 1 study in healthy participants to characterize the safety and pharmacology of inclacumab, a fully human anti-P-selectin antibody, in development for treatment of sickle cell disease

    Purpose

    We evaluated the safety, pharmacokinetics (PK), pharmacodynamics (PD), and immunogenicity of intravenous (IV) inclacumab, a fully human IgG4...

    Christina Lourdes Mayer, Kathleen Koeck, ... Patrick Yue in European Journal of Clinical Pharmacology
    Article Open access 12 July 2023
  13. Manifestations of HbSE sickle cell disease: a systematic review

    Background

    Sickle cell disease (SCD) is commonly encountered in Africa and Middle Eastern countries. The causative mutation in the gene encoding the...

    Ibrahim Khamees, Fateen Ata, ... Mohamed A. Yassin in Journal of Translational Medicine
    Article Open access 16 June 2021
  14. Comparative evaluation of different oral iron salts in the management of iron deficiency anemia

    Background

    Anemia affects one-fourth of the world's population and is caused mostly by iron deficiency. Iron supplementation is the most essential...

    Manoj A. Suva, Pravin R. Tirgar in DARU Journal of Pharmaceutical Sciences
    Article 14 May 2024
  15. Analysis of red blood cells from peripheral blood smear images for anemia detection: a methodological review

    Anemia is a blood disorder which is caused due to inadequate red blood cells and hemoglobin concentration. It occurs in all phases of life cycle but...

    Navya K.T., Keerthana Prasad, Brij Mohan Kumar Singh in Medical & Biological Engineering & Computing
    Article Open access 15 July 2022
  16. Effect of Gum Arabic (Acacia senegal) on C-reactive protein level among sickle cell anemia patients

    Objectives

    Inflammation is ongoing process among sickle cell anemia even during steady state. C reactive protein (CRP) is cardinal marker that...

    Lamis AbdelGadir Kaddam, Anas Suliman Kaddam in BMC Research Notes
    Article Open access 18 March 2020
  17. Sickle cell trait newborn screen results: disclosure and management

    This study aims to evaluate the notification process of sickle cell trait (SCT) identified by newborn screening in Alberta. On April 1, 2019, Alberta...

    Margaret Lilley, Stephanie Hoang, ... Susan Christian in Journal of Community Genetics
    Article 26 October 2020
  18. Clinical and biochemical characteristics, and outcome in 33 patients with ceftriaxone-induced liver injury

    Purpose

    To summarize the clinical and biochemical characteristics of patients with ceftriaxone-induced liver injury and guide the selection of safe...

    Cai-**a Feng, Wen-Yu Ye, Qing-Wen Shan in European Journal of Clinical Pharmacology
    Article 29 May 2024
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