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ology for emergency surgical or percutaneous airways, to facilitate clear crisis communication. Dilated cardiomyopathy (DCM) is a complex disease where genetics interplay with extrinsic factors. This study aims to compare the phenotype, management, and outcome of familial DCM (FDCM) and non-familial (sporadic) DCM (SDCM) across Europe. Patients with DCM that were enrolled in the prospective ESC EORP Cardiomyopathy Myocarditis Registry were included. Baseline characteristics, genetic testing, genetic yield, and outcome were analyse
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