ArticleEJHaem2025
Enhanced Disease Detection of Hairy Cell Leukaemia Through Next-Generation Sequencing Based
Article in EJHaem, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
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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
0 citing papers in PubMed.
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Authors and funding
13 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Introduction: Longitudinal disease assessment by molecular techniques is not routine in hairy cell leukaemia (HCL). Combining Results: Conclusion: Through multiple patient-specific genomic targets to improve sensitivity, NGS may potentially improve disease detection in HCL. Trial Registration: The authors have confirmed clinical trial registration is not needed for this submission.
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Registered trials
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