Familial right ventricular dilated cardiomyopathy.
Cardiomyopathy of unknown cause occurred in three of six siblings. The course of the illness was marked by life threatening supraventricular and ventricular arrhythmias, sinoatrial block, atrioventricular block, and embolism (in one patient). The disease was characterised by right ventricular dilata...
שמור ב:
| הוצא לאור ב: | Br Heart J |
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| Principais autores: | , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
BMJ Publishing Group
1985
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC481871/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/4015925/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/hrt.54.2.156 |
| תגים: |
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