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Characterization and Clinical Management of Dilated Cardiomyopathy, Hardcover/Marco Merlo - Mdpi AG


Characterization and Clinical Management of Dilated Cardiomyopathy, Hardcover/Marco Merlo
342 Lei

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(15-11-2024)
Cumpara de la elefant.ro

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Dilated Cardiomyopathy (DCM) is a particular phenotype of non-ischemic systolic heart failure, frequently recognizing a genetic background and affecting relatively young patients with few comorbidities.
Nevertheless, DCM is still one of the most common causes of heart transpl.
Nowadays, long-term survival of DCM patients has been markedly improved due to an early diagnosis and uninterrupted and tailored follow-up under constant optimal medical and non-pharmacological evidence-based treatments.
Dilated Cardiomyopathy (DCM) is a particular phenotype of non-ischemic systolic heart failure, frequently recognizing a genetic background and affecting relatively young patients with few comorbidities


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