Pancreatic iron loading in chronically transfused sickle cell disease is lower than in thalassaemia major
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.2010.08476.x/fullpdf
Reference19 articles.
1. Spleen R2 and R2* in iron-overloaded patients with sickle cell disease and thalassemia major;Brewer;Journal of Magnetic Resonance Imaging,2009
2. Effect of transfusional iron intake on response to chelation therapy in beta-thalassemia major;Cohen;Blood,2008
3. Increased prevalence of iron-overload associated endocrinopathy in thalassaemia versus sickle-cell disease;Fung;British Journal of Haematology,2006
4. Morbidity and mortality in chronically transfused subjects with thalassemia and sickle cell disease: a report from the multi-center study of iron overload;Fung;American Journal of Hematology,2007
5. Disparity in the management of iron overload between patients with sickle cell disease and thalassemia who received transfusions;Fung;Transfusion,2008
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1. Rapid MRI Assessment of Long‐Axis Strain to Indicate Systolic Dysfunction in Patients With Sickle Cell Disease;Journal of Magnetic Resonance Imaging;2023-02-15
2. The role of MRI-R2* in the detection of subclinical pancreatic iron loading among transfusion-dependent sickle cell disease patients and correlation with hepatic and cardiac iron loading;Insights into Imaging;2022-09-04
3. Frequency, pattern, and associations of renal iron accumulation in sickle/β-thalassemia patients;Annals of Hematology;2022-07-11
4. Relationship between pancreatic iron overload, glucose metabolism and cardiac complications in sickle cell disease: An Italian multicentre study;European Journal of Haematology;2022-07-08
5. Pancreatic iron quantification with MR imaging: a practical guide;Abdominal Radiology;2022-05-21
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