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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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| Veröffentlicht in: | Heart |
|---|---|
| Hauptverfasser: | , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BMJ Publishing Group
2017
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| Schlagworte: | |
| Online Zugang: | 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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