Hydroxyurea for Children with Sickle Cell Anemia in Sub-Saharan Africa

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Items 301–380 of 380

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    Dyego Luis Cavalcante Lacerda, Roneiza Soares Rufino, Jeanille Seixas Xavier Abrantes Diniz, Ankilma do Nascimento Andrade Feitosa, Bruno Menezes de Carvalho, Thárcio Ruston Oliveira Braga · 2023 · Pimenta Cultural eBooks
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  13. Linking replication stress with replication dynamics in Vicia faba root meristem cells
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  14. Sickle Cell Anemia in Children in Sub-Saharan Africa—What Is the Best Medicine?
    Timothy S. Laux · 2023 · Oxford University Press eBooks
  15. Sickle-Cell Diseases
    Cage Saul Johnson · 2024 · Elsevier eBooks
  16. Sociodemographic and Clinical Characteristics and the Impact of Hydroxyurea on Laboratory Profile and Healthcare Resource Utilization of Adult Patients with Sickle Cell Disease: An Observational and Retrospective Study of 5 Years of Follow-Up in a Reference Center in Brazil
    Rodolfo Delfini Cançado · 2023 · Haematology International Journal
  17. The Impact of Hydroxyurea Use on Cognitive Functioning of Children with Sickle Cell Disease Living in Ghana
    Olubusola B. Oluwole, Mary Akua Ampomah, Amma Twumwa Owusu-Ansah, Mehdi syed Nouraie, Catherine Idara Segbefia, Enrico Maria Novelli · 2024
  18. Fixed Low-Dose Hydroxyurea Therapy: A Strategy for Reducing Emergency Room Visits and Improving Treatment Adherence in Paediatric Sickle Cell Anaemia in Resource-Limited Settings
    Chisom Adaobi Nri-Ezedi, N I Ugwu, Thomas Obiajulu Ulasi · 2024
  19. Comprehensive Insights into Hydroxyurea Treatment for Children with Sickle Cell Disease: A Critical Review
    Rajesh Hadia · 2024 · Asian Journal of Pharmaceutics
  20. Human Immunodeficiency Virus Co-Infection among Sickle Cell-Exposed Children in Kisumu County, Western Kenya
    Ottoman Adel, Raphael Wekesa Lihana, Betsy Chebet Rono · 2024 · International Journal of Scientific Research and Management (IJSRM)
  21. Platelet-Neutrophil Ratio: A Novel Monitoring Tool for Sickle Cell Anaemia in Resource-Limited Settings
    Chisom Adaobi Nri-Ezedi, Thomas Obiajulu Ulasi, Chilota Chibuife Efobi, John Aneke, N I Ugwu, Chinekwu Nwosu · 2024
  22. Ingesta diaria de líquidos y uso de hidroxiurea en pacientes con enfermedad falciforme de un centro de referencia de Cartagena de Indias, Colombia
    Óscar Giovanny Iglesias-Jiménez, Rita Magola Sierra Merlano · 2024 · Revista Colombiana de Hematología y Oncología
  23. Malaria prophylaxis in sickle cell anaemia: some answers, more questions
    Thomas Neil Williams, Russell E. Ware · 2024 · The Lancet Infectious Diseases
  24. Advances in transfusion therapy of packed red blood cells in patients with sickle cell disease, complementary pharmacology and emerging treatments
    Boris Daniel Albán Espín, Elena Johanna Pérez Laborde · 2024 · Salud Ciencia y Tecnología
  25. Impact Of Hydroxyurea Adherence Levels On Hematological And Clinical Outcomes In Children With Sickle Cell Disease: A Systematic Review In Sub-Saharan Africa
    PIVADGA COLLINS, Ehimen P. Odum, B. A. Alex-Hart · 2025
  26. The role of hydroxyurea and the clinical outcome of paediatric sickle cell disease patients in a tertiary hospital in North-western Nigeria
    Hauwa A. Muhammad, Auwal Garba Suleiman, AA Umar, Mu’awiyyah Babale Sufiyan · 2025 · Journal of Community Medicine and Primary Health Care
  27. Factores de riesgo asociados a alteraciones nutricionales en niños con anemia de células falciformes
    Suanny González Coquel, Dahify Martelo Manjarrez, Amada Puello Moscote, Luisa Gonzalez Ángel · 2024 · Revista Ciencias Biomédicas
  28. Clinical consultation: The pharmacist’s role in hydroxyurea management for sickle cell disease
    Cameron Roessner, Kelsey Uminski, Dawn M. Goodyear, Natalia Rydz · 2025 · American Journal of Health-System Pharmacy
  29. Morbidity, Mortality, and Management of Sickle Cell Disease in Africa Before and During the Covid-19 Pandemic: A Multinational Hospital-Based Retrospective Cohort Study
    Jean Bisimwa Nachega, Rhoderick Neri Machekano, Philip Jon Rosenthal, Léon Muepu Tshilolo, Benjamin Kasongo Kabulo, Brígida Santos, Ntumba A.M. Tima, Lurdes YD, Obiageli Eunice Nnodu, Ayomide Esther Fasina et al. · 2025 · SSRN Electronic Journal
  30. Assessment of Diagnostic and Clinical Facilities for Sickle Cell Disease at the National Institute of Oncology, Sabratha, Libya
    Haleemah Abdulrahman, Ali Madour · 2025 · Khalij-Libya Journal of Dental and Medical Research
  31. Clinical and Laboratory Correlates of Cerebral Blood Flow Velocities and Risks for Stroke Among Steady-State Sickle Cell Anemia Children: A Cross-Sectional Study
    Oyetoke Christina Oderanti, Samuel Olorunyomi Oninla, Moshood Adebayo Akintola, Olawale A. Abayomi, Funso Abidemi Olagunju, Funmilola J. Adesokan · 2025 · Cureus
  32. Systematic and Bibliometric Insights of Over Seven Decades of Sickle Cell Disease Research in Africa
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  33. Strengthening the Sickle Cell Care Pipeline: a Systems-Based Approach in Sierra Leone
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  35. Hydroxyurea utilization among individuals with sickle cell disease in Tennessee: a pooled analysis of claims data
    Ayesha Mukhopadhyay, Matthew Paul Smeltzer, Judy Dudley, Sherif M. Badawy, Joacy G. Mathias, Allison P. Plaxco, Meredith A. Ray, Andrew David Wiese, Walter I. Stevens, James G. Gurney et al. · 2025 · Frontiers in Pharmacology
  36. Additional file 1 of Evaluation of treatment patterns, healthcare resource utilization and cost of illness for sickle cell disease in Ghana: a private medical insurance claims database study
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  37. Use of Hydroxyurea in Severe Forms of Sickle Cell Disease: Study of 60 Pediatric Cases in Senegal
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  38. Profil des adolescents atteints de syndrome drépanocytaire majeur suivis au service de pédiatrie du Centre Hospitalier Universitaire de Cocody en République de Côte d’Ivoire
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  39. Continuum of care after newborn screening for sickle cell disease: Multinational evidence from a systematic review and meta‐analysis
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  40. Cost-Effectiveness of Hydroxyurea for Treatment of Children With Sickle Cell Anemia in Ghana
    Sinaï Francisco Dias, Brian Adu Asare, Lumbwe Chola · 2026 · Value in Health Regional Issues
  41. Clinical and Laboratory Characteristics of Adolescents and Young Adults with Sickle Cell Disease at Steady State in Uganda
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  42. Path To Sickle Cell Disease Elimination in India: from Precision Diagnostics and Comprehensive Care To Curative Horizons
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  43. Emerging concepts in sickle cell disease acute chest syndrome
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  45. Awareness, Acceptability and Outcome of Newborn Screening for Sickle Cell Disease in Benue State, Nigeria
    A. Michael, Olugbenga Mokuolu · 2025 · Nigerian Journal of Paediatrics
  46. Acute Complications of Major Sickle Cell Syndromes in Libreville, Gabon: Clinical and Paraclinical Aspects
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  47. Assessing quality of life and hematological parameters in children with sickle cell disease: a cross-sectional study in Bukavu, Democratic Republic of the Congo
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  48. Aqueous Extract of Ceiba pentandra Stimulates the Production of Fetal Hemoglobin in Sickle Cell Patients
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  49. Clinical and laboratory characteristics of adolescents and young adults with sickle cell disease at steady state in Uganda
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  50. Systematic literature review on hydroxyurea treatment of SCD in low- to middle-income countries
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  52. The challenge of treating African children with hydroxyurea
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  53. Subclinical malaria in sickle cell disease in Northern Uganda: prevalence, predictors, and hematologic impact
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  54. Incidence and risk factors for vaso occlusive crisis among children living with sickle cell disease in Uganda: a cohort study
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  55. Trends in the burden of sickle cell disorders in Sierra Leone, 1990–2023: An analysis of Global Burden of Disease Study 2023 estimates
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  56. Early presentation of Sickle Cell Disease in a two-month-old infant: A case report
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  58. Hydroxyurea for the Prevention of Stroke in Sickle Cell Anaemia: Mechanisms, Clinical Trial Evidence, and Global Implementation
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  59. An assessment of the effectiveness of hydroxyurea therapy in children and adolescents with sickle cell anaemia at Kenyatta National Hospital
    Madline Yacoub-Kenyi Leju, Amsalu Degu · 2026 · Annals of Hematology
  60. Diagnostic Classification Model of Vaso-Occlusive Crises Based on Oxidative, Inflammatory and Metabolic Biomarkers in Congolese Sickle Cell Patients
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  61. Oxygen Timing as Therapy: Molecular Rationale and Clinical Imperative for Early Oxygen Administration in the Sickle Cell Disease Vaso-Occlusive Crisis—A Structured Narrative Review with Implications for Resource-Constrained Health Systems
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  62. Impact of hydroxyurea use on severity and hematologic profile in children with sickle cell disease at University of Benin Teaching Hospital, Benin city, Nigeria
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  63. Perspective Chapter: Fetal Hemoglobin Modulators
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  64. Hydroxyurea adherence and treatment outcomes in pediatric sickle cell disease: a prospective cohort study
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  65. Global research trends and influential contributions in sickle cell disease: a bibliometric analysis of the top 100 cited papers
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  66. Hydroxyurea Dose Escalation to Maximum Tolerated Dose in Pediatric Sickle Cell Disease: Hematologic and Clinical Outcomes in a Resource-Limited Setting in Cameroon. A Quasi-Experimental Study.
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  67. Hydroxyurea treatment for sickle cell disease in Nairobi informal settlements: a retrospective cohort study
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  68. Financing Sickle Cell Disease Like it Matters
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  69. Evaluation of hydroxyurea effect in patients with sickle cell disease: A prospective observational study
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  70. Validation of the Gazelle point-of-care device for hemoglobin variant analysis in a predominantly pediatric population: performance comparison with conventional electrophoresis
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  71. RESOLVE to do better
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  72. Oxidative Stress Burden in Paediatric Sickle Cell Anaemia: Effects of Hydroxyurea Therapy, Disease Severity, and Socioeconomic Factors
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  73. Incidence of clinically diagnosed infections in children with sickle cell anaemia treated with oral hydroxyurea in Angola, DR Congo, Kenya, and Uganda: a retrospective cohort study from the REACH trial
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  74. A national spatial prioritisation framework for the targeted expansion of essential sickle cell disease services across health-facility catchments in Uganda
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  75. A systematic review of advances and challenges in stroke prevention in sickle cell disease since the STOP trials
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  77. The CRISPR Era and Beyond: Technical Milestones and Future Directions in Sickle Cell Disease Therapeutics
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  78. Le traitement par hydroxyurée dans les syndromes drépanocytaires majeurs de l’adulte : recommandations françaises 2026
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  79. Neurological complications of sickle cell anaemia and malarial anaemia in low- and middle-income countries: a narrative review
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  80. Factors Associated with Abnormal Transcranial Doppler and Stroke Risk in Children with Sickle Cell Disease Followed at the Center for Research and Control of Sickle Cell Disease (CRLD) in Mali
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