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Light-chain cardiac amyloidosis: strategies to promote early diagnosis and cardiac response

Amyloid light chain (AL) amyloidosis is a systemic disease characterised by the aggregation of misfolded immunoglobulin light chain (LC), predominantly in the heart and kidneys, causing organ failure. If untreated, the median survival of patients with cardiac AL amyloidosis is 6 months from the onse...

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Detaylı Bibliyografya
Yayımlandı:Heart
Asıl Yazarlar: Grogan, Martha, Dispenzieri, Angela, Gertz, Morie A
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BMJ Publishing Group 2017
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5566095/
https://ncbi.nlm.nih.gov/pubmed/28456755
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/heartjnl-2016-310704
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