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The natural history of hypertrophic cardiomyopathy

In the early years of the disease recognition, hypertrophic cardiomyopathy (HCM) was viewed as an ominous disease with unfavourable prognosis and with an annual mortality between 4% and 6%. At that time, 73% of the patients reported in the literature came from only two referral centres. With the int...

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Detaylı Bibliyografya
Yayımlandı:Eur Heart J Suppl
Asıl Yazarlar: Autore, Camillo, Musumeci, Maria Beatrice
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Oxford University Press 2020
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7904071/
https://ncbi.nlm.nih.gov/pubmed/33654461
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/eurheartj/suaa125
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