Longitudinal Study of Survival and Causes of Death in Patients with Thalassemia Major in Greece
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- Type
- article
- Published
- 2005-11-01
- Cited by
- 114
- References
- 7
- OpenAlex
- https://openalex.org/W2042609716
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:11313940
Keywords
Medicine, Thalassemia, Hemosiderosis, Sepsis, Internal medicine
References
- Prolonged survival in patients with beta-thalassemia major treated with deferoxamine.
- Survival and Disease Complications in Thalassemia Major
- Survival in β-thalassaemia major in the UK: data from the UK Thalassaemia Register
- Molecular characterization of β‐thalassaemia in 174 Greek patients with thalassaemia major
- Monitoring chelation therapy to achieve optimal outcome in the treatment of thalassaemia.
- Combined therapy with desferrioxamine and deferiprone in thalassemic patients: effect on urinary iron excretion.
- Monitoring chelation therapy to achieve optimal outcome in the treatment of thalassaemia
Cited by
- Current Trends in the Management of Beta Thalassemia
- Awareness among parents of children with thalassemia major.
- Iron-Chelating Therapies in a Transfusion-Dependent Thalassaemia Population in Thailand
- Development and Validation of a Multidimensional Expectation Questionnaire for Thalassaemia Major Patients
- Early impairment of myocardial function in young patients with β‐thalassemia major
- Relation of chelation regimes to cardiac mortality and morbidity in patients with thalassaemia major: an observational study from a large Greek Unit
- Anemia and Iron Management
- Sustained Ventricular Tachycardia in a Patient with Thalassemia Major
- Heart Rate Variability for Early Detection of Iron Overload Cardiomyopathy in β-Thalassemia Patients
- Cardiac magnetic resonance in transfusion dependent thalassaemia: assessment of iron load and relationship to left ventricular ejection fraction
- Treating thalassemia major-related iron overload: the role of deferiprone
- Erythropoiesis-stimulating agents in the treatment of anemia in myelodysplastic syndromes: a meta-analysis
- Cardiovascular function and treatment in β-thalassemia major: a consensus statement from the American Heart Association.
- Malignancies in patients with β‐thalassemia major and β‐thalassemia intermedia: A multicenter study in Iran
- In search of the optimal iron chelation therapy for patients with thalassemia major
- Pharmacoeconomic Considerations in Treating Iron Overload in Patients with β-Thalassaemia, Sickle Cell Disease and Myelodysplastic Syndromes in the US
- A national registry of haemoglobinopathies in Greece: Deducted demographics, trends in mortality and affected births
- Hepatitis B and C Infections in Multitransfused Thalassemic Patients
- Hepatitis C in patients with β-thalassemia major. A single-centre experience
- Cardiac mortality in β‐thalassemia major: resting but not dobutamine stress echocardiography predicts mortality among initially cardiac disease‐free patients in a prospective 12‐year study
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