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Multimodality imaging in cardiomyopathies

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Babur Güler G., Gürsoy M.O., Tan Kürklü T.S., Yakar Tülüce S., Karaca Ɩzer P., Karabulut D., Hatipoğlu S., BarutƧu A., KılıƧgedik A., Güler A., Uygur B., İzgi C., Yıldız C., ƇiƧek Yılmaz D., GenƧ Albayrak D., İnan D., Ɩzpelit E., Eroğlu Büyükƶner E., Güçlü E., Vatansever Ağca F., Ƈağlıyan F., Akyıldız AkƧay F., Kahveci G., Ƈelik H.G., Altun İ., Altun İ., DinƧer İ., Türkmen İ., Ohtaroğlu Tokdil K., Arslan M., Karacan M., Akbulut M., Turan Şerifler N., TüfekƧioğlu O., SeƧkin Gƶbüt Ɩ., Yıldırımtürk Ɩ., Acar R.D.,Yƶndem S., Sert Şekerci S., Ünlü S., Üstündağ S., Karagƶz U., Kumral Z., Bayram Z.

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Kardiyomiyopatilerde multimodalite görüntüleme

Abstract

Cardiomyopathy, which is shortly defined as a disease of the myocardium, has a broad definition that includes many different diagnoses. Recent advances in cardiac imaging techniques, including basic and advanced echocardiography, computed tomography, nuclear medicine, and cardiac magnetic resonance, allow for a more accurate evaluation of volumes and thickness of cardiac chambers, systolic and diastolic function of the ventricules, and tissue structure. Multimodality imaging often provides the first clinical suspicion for specific etiologies, especially when the medical and family history is unclear, by identification of red flags of underlying systemic diseases. In this review, we aimed to evaluate the role of multimodality imaging in diagnosis of cardiomyopathies with key images and discussed the effects of genetics on the diagnostic, prognostic, and therapeutic guidance of cardiomyopathies.

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Kare Publishing

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Türk Kardiyoloji Derneği Arşivi

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DOI

10.5543/tkda.2024.13636

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CC BY-NC-ND (Attribution-NonCommercial-NoDerivs)

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Except where otherwise noted, this item's license is described as CC BY-NC-ND (Attribution-NonCommercial-NoDerivs)

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