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Assessment of the relationship between fragmented QRS and cardiac iron overload in patients with beta-thalassemia major

OBJECTIVE: Beta-thalassemia major (TM) is a genetic hemoglobin disorder causing chronic hemolytic anemia. Since cardiac insufficiency and arrhythmias are the primary causes of mortality in such patients, monitoring of cardiac iron load is important in management of the disorder. The purpose of this...

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Publicat a:Anatol J Cardiol
Autors principals: Bayar, Nermin, Kurtoğlu, Erdal, Arslan, Şakir, Erkal, Zehra, Çay, Serkan, Çağırcı, Göksel, Deveci, Burak, Küçükseymen, Selçuk
Format: Artigo
Idioma:Inglês
Publicat: Kare Publishing 2015
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5336998/
https://ncbi.nlm.nih.gov/pubmed/25252297
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5152/akd.2014.5188
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