טוען...
Noninvasive diagnosis of hereditary transthyretin-related cardiac amyloidosis: A case report
RATIONALE: Cardiac transthyretin amyloidosis is a progressive and fatal cardiomyopathy for which several promising therapies are in development. The diagnosis is frequently delayed or missed because of the limited specificity of clinical manifestations, routine electrocardiogram, echocardiography an...
שמור ב:
| הוצא לאור ב: | Medicine (Baltimore) |
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| Main Authors: | , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Wolters Kluwer Health
2019
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6709038/ https://ncbi.nlm.nih.gov/pubmed/31348283 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000016566 |
| תגים: |
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