Research map: The Need for Standardization of MRI Methods for Measuring LIC for the Management of Iron Overload in Patients with Hemoglobinopathies
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Papers in this map
Quantification of Liver Iron Overload with MRI: Review and Guidelines from the ESGAR and SAR
· Scott B. Reeder · 2023 · 169 citations · Cited by this paper
Two Novel δ-Globin Chain Variants Identified in the Chinese Population
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Guidelines for the monitoring and management of iron overload in patients with haemoglobinopathies and rare anaemias
· Farrukh Shah · 2021 · 60 citations · Cited by this paper
Encouraging Outcomes of Hematopoeitic Stem Cell Transplantation in Pediatric Sickle Cell Disease- A Decade-Long Experience from the Developing World
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MRI Measurements of Iron Load in Transfusion-Dependent Patients: Implementation, Challenges, and Pitfalls
· Charles T. Quinn · 2015 · 34 citations · Cited by this paper
SickleInAfrica Consortium: A Seven-Country Study Evaluating the Performance of Dried Blood Spot Point-of-Care Testing in Newborn Screening for Sickle Cell Disease
· 2026 · Related
Best Practices in Gene Therapy for Sickle Cell Disease and Transfusion-dependent β-Thalassemia
· Haydar Frangoul · 2025 · 12 citations · Cited by this paper
Two Novel SUPT5H Variants Causing β-Thalassemia Trait Phenotypes
· 2026 · Related
Comparison of liver MRI R2(FerriScan®) VS liver MRI T2* as a measure of body iron load in a cohort of beta thalassaemia major patients
· Padmapani Padeniya · 2020 · 11 citations · Cited by this paper
Expression Differences of Abnormal Hemoglobin New York in Infants, Children and Adults, and Analysis of Clinical Phenotypes and Genotypes in Combination with Thalassemia
· 2026 · Related
Narrative review of magnetic resonance imaging in quantifying liver iron load
· Qing Feng · 2024 · 9 citations · Cited by this paper
Comparative Analysis of Erythroferrone and Hepcidin as Emerging Biomarkers of Iron Homeostasis in Patients with β-Thalassemia Major: A Case-Control Study from Pakistan
· 2026 · Related
Reproducibility of liver iron concentration measured by R2* method based on 1.5-T MRI: a meta-analysis
· Sue Cao · 2025 · 1 citation · Cited by this paper
Identification of a New δ chain hemoglobin Variant, Hb A2-Malay [δ46(CD5)Gly > Arg, HBD : C.139G > C;316-443A > G]
· 2025 · Related
Molecular Diagnosis and Stability Testing of Hemoglobin Phnom Penh [ HBA1 : C.353_355dup (p.Phe118_Thr119insIle)] – The First Northern Thai Case
· 2025 · Related
Pituitary Versus Hepatic Iron Assessment in Transfusion-Dependent Thalassemia: Is Signal Intensity Ratio a Reliable Tool?
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A Diverse Genetic Landscape: Thalassemia Genotype Patterns in Myanmar and Cambodian Workers in Southern Thailand
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