β-thalassemia trait and iron overload: is it time to consider oral iron chelators? Comments on: “A case series of patients with A-thalassemia trait and iron overload: from multifactorial hepcidin suppression to treatment with mini-phlebotomies”

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Publication Details

Journal
Haematologica
Published
2025-08-28
DOI
https://doi.org/10.3324/haematol.2025.288578
Primary Topic
Hemoglobinopathies and Related Disorders
Type
article
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article

β-thalassemia trait and iron overload: is it time to consider oral iron chelators? Comments on: “A case series of patients with A-thalassemia trait and iron overload: from multifactorial hepcidin suppression to treatment with mini-phlebotomies”

Alberto Piperno, Raffaella Mariani
Haematologica
Hemoglobinopathies and Related Disorders
article

β-thalassemia trait and iron overload: is it time to consider oral iron chelators? Comments on: “A case series of patients with A-thalassemia trait and iron overload: from multifactorial hepcidin suppression to treatment with mini-phlebotomies”

Alberto Piperno, Raffaella Mariani
article en

Abstract

No abstract available for this paper.
HaematologicaVol. 111(2)
Azienda Ospedaliera San Gerardo (IT), University of Milano-Bicocca (IT)
Openalex Percentile: Top 69%
Hemoglobinopathies and Related Disorders
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β-thalassemia trait and iron overload: is it time to consider oral iron chelators? Comments on: “A case series of patients with A-thalassemia trait and iron overload: from multifactorial hepcidin suppression to treatment with mini-phlebotomies” — Alberto Piperno, Raffaella Mariani · Haematologica (2025) | TGRS Research Map | TGRS