Prevalence and clinical correlates of QT prolongation in patients with hypertrophic cardiomyopathy

AIMS: Congenital or acquired QT prolongation is a risk factor for life-threatening arrhythmias. In patients with hypertrophic cardiomyopathy (HCM), the QT interval may be intrinsically prolonged. However, the prevalence, cause, and significance of QT prolongation among patients with HCM are unknown....

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Johnson, Jonathan N., Grifoni, Camilla, Bos, J. Martijn, Saber-Ayad, Maha, Ommen, Steve R., Nistri, Stefano, Cecchi, Franco, Olivotto, Iacopo, Ackerman, Michael J.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Oxford University Press 2011
Gaiak:
Clinical Research
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC3086898/
https://ncbi.nlm.nih.gov/pubmed/21345853
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/eurheartj/ehr021
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