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  1. Sickle Cell Disease

    Sickle cell disease (SCD) is a monogenetic disease with a polygenic phenotype. Stroke and other cerebrovascular diseases are still among the most...
    N. Abimbola Sunmonu, Robert J. Adams, ... Hyacinth I. Hyacinth in Stroke Genetics
    Chapter 2024
  2. Surgery for Sickle Cell Retinopathy

    This chapter discusses the indications, surgical considerations, and techniques for managing proliferative sickle cell-related vitreoretinal...
    Riley Sanders, Kwesi Nyan Amissah-Arthur in Practical Manual of Vitreoretinal Surgery
    Chapter 2024
  3. Sickle Cell Retinopathy

    Sickle cell disease is the most common inherited hematological disorder worldwide. Ocular manifestations of SCD include sickle cell retinopathy (SCR)...
    Ishrat Ahmed, Adrienne W. Scott in Pediatric Vitreoretinal Surgery
    Chapter 2023
  4. Sickle Cell Anemia and Related Hemoglobinopathies

    Sickle cell disease (SCD)is the most common structural hemoglobinopathies resulting from inherited abnormalities of globin chain synthesis. This...
    Chapter 2024
  5. Sickle Cell Anemia and Ulcer

    Sickle cell hemoglobin (HbS) is a variant of adult hemoglobin due to mutation of beta chain of globin, which leads to substitution of valine amino...
    Rajniti Prasad, Meenakshi Pandey in Uncommon Ulcers of the Extremities
    Chapter 2023
  6. Non-Sickle Cell Structural Hemoglobinopathies

    Hemoglobinopathies are common inherited diseases around the world. There are many structural hemoglobin variants. Examples of non-sickle cell...
    Chapter 2024
  7. Hemoglobinopathies (Sickle Cell Disease and Thalassemia)

    Hematopoietic cell transplantation (HCT) using an HLA-matched sibling donor is a well-established curative therapy for pediatric patients with sickle...
    Barbara Cappelli, Eliane Gluckman, ... Miguel R. Abboud in The EBMT Handbook
    Chapter Open access 2024
  8. The Kidney in Sickle Cell Disease

    Early in life, patients with sickle cell anemia are at high risk for the development of hyposthenuria, enuresis, and hyperfiltration. Importantly,...
    Jeffrey Lebensburger, Cristin Kaspar in Pediatric Kidney Disease
    Chapter 2023
  9. Comparative assessment of quality of life among adolescents with sickle cell disease and sickle cell trait: evidence from Odisha, India

    The present study aims to assess the quality of life (QOL) of adolescents with sickle cell disease (SCD) and sickle cell trait (SCT) in hard-to-reach...

    Basanta Kumar Bindhani, Jayanta Kumar Nayak in Journal of Community Genetics
    Article 08 April 2024
  10. How I Manage Sickle Cell Retinopathy

    Purpose of Review

    We describe our current approach to sickle cell retinopathy screening, evaluation, treatment, and surgical intervention.

    ...
    Christina M. Ambrosino, Adrienne W. Scott in Current Surgery Reports
    Article 21 June 2024
  11. New Insights into Clinical Management for Sickle Cell Disease: Uncovering the Significant Pathways Affected by the Involvement of Sickle Cell Disease

    One of the severe monogenic conditions with the highest prevalence in the globe is sickle cell disease. Although the significance of chronic anemia,...
    Usha Chouhan, Trilok Janghel, ... Jyoti Kant Choudhari in Reverse Engineering of Regulatory Networks
    Protocol 2024
  12. Sickle Cell Retinopathy

    Sickle cell retinopathy prevalence increases with age and occurs earlier in patients with hemoglobin SC than with hemoglobin SS or SThalassemia...
    Reference work entry 2022
  13. 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
  14. Social Science Research and Sickle Cell Disorders

    Social science research on sickle cell disorders (SCD), recessively inherited blood conditions, have come of age in the last twenty years from being...
    Living reference work entry 2023
  15. Social Science Research and Sickle Cell Disorders

    Social science research on sickle cell disorders (SCD), recessively inherited blood conditions, have come of age in the last twenty years from being...
    Reference work entry 2023
  16. Sickle Cell Disease

    Sickle cell disease (SCD) is caused by a structurally abnormal β-globin chain, expressed exclusively in erythrocytes and incorporated in Sickle...
    Chapter 2022
  17. Statistical Analysis of Hematological Parameters for Prediction of Sickle Cell Disease

    About 30 million people worldwide are affected by the monogenic recessive -globin gene abnormality known as sickle cell disease (SCD), which is a...
    Bhawna Dash, Soumyalatha Naveen, UM Ashwinkumar in Cognitive Computing and Cyber Physical Systems
    Conference paper 2024
  18. Sickle Cell Disease Management in Develo** Countries

    Sickle cell disease (SCD) remains a formidable healthcare challenge in develo** countries, characterized by high prevalence, significant morbidity,...
    Living reference work entry 2024
  19. The Use of Natural Products in the Treatment of Sickle Cell Disease

    Sickle cell disease is the world's leading inherited genetic hemoglobinopathy, originating from African peoples, characterized by the presence of...

    Rebeca Garcia de Paula, Hewerthon Medrado Ribeiro, ... Carla Simone Seibert in Revista Brasileira de Farmacognosia
    Article 29 March 2024
  20. Risk factors associated with sickle cell retinopathy: findings from the Cooperative Study of Sickle Cell Disease

    Background

    Sickle cell retinopathy (SCR) is one of the most important ocular manifestations of sickle cell disease (SCD). This study aims to assess...

    Mohammed Nawaiseh, Allaa Roto, ... Nakhleh Abu-Yaghi in International Journal of Retina and Vitreous
    Article Open access 22 September 2022
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