Sickle cell anemia: clinical diversity and beta S-globin haplotypes.

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

Who cites it

17 citing papers in PubMed.

1. Gene-environmental influence of space and microgravity on red blood cells with sickle cell disease.NPJ genomic medicine · 2024
   Review
2. Frequency of beta S globin gene haplotypes among sickle cell patients in Nigeria.The Journal of international medical research · 2021
   Article
3. Genotypic Diversity among Angolan Children with Sickle Cell Anemia.International journal of environmental research and public health · 2021
   Article
4. Non-S Sickling Hemoglobin Variants: Historical, Genetic, Diagnostic, and Clinical Perspectives.Oman medical journal · 2021
   Review
5. Alpha thalassemia, but not βAnnals of hematology · 2021
   Article
6. A Cross-Sectional Study of Detection of Beta Globin (HBB) Haplotypes Among Beta Thalassemia Patients.Cureus · 2021
   Article
7. The Sickle Effect: The Silent Titan Affecting Glycated Hemoglobin Reliability.Cureus · 2020
   Review
8. High fetal hemoglobin level is associated with increased risk of cerebral vasculopathy in children with sickle cell disease in Mayotte.BMC pediatrics · 2020
   Article
9. A chaotic viewpoint-based approach to solve haplotype assembly using hypergraph model.PloS one · 2020
   Article
10. Influence of beta-cluster haplotypes, alpha-gene status and UGTA1 polymorphism on clinical and hematological data in sickle-cell disease children from French Guiana.PloS one · 2020
    Article
11. Genetic comparison of sickle cell anaemia cohorts from Brazil and the United States reveals high levels of divergence.Scientific reports · 2019
    Article
12. Influence of β-Globin Haplotypes on Oxidative Stress, Antioxidant Capacity and Inflammation in Sickle Cell Patients of Chhattisgarh.Indian journal of clinical biochemistry : IJCB · 2019
    Article
13. Understanding the contrasting spatial haplotype patterns of malaria-protective β-globin polymorphisms.Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases · 2015
    Article
14. Association of erythrocytes antioxidant enzymes and their cofactors with markers of oxidative stress in patients with sickle cell anemia.Qatar medical journal · 2015
    Article
15. Craniofacial features of patients with sickle cell anemia and sickle cell trait.The Angle orthodontist · 2014
    Article
16. Relationship between pulmonary and cardiac abnormalities in sickle cell disease: implications for the management of patients.Revista brasileira de hematologia e hemoterapia
    Article
17. Histopathological Features of Sickle Cell Nephropathy in the Arab-Indian Haplotype.Glomerular diseases
    Article

Corrections and comments

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Authors and funding

1 author.

Funding

No grant is acknowledged in the PubMed record.

Abstract

PubMed holds no abstract for this paper.