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Dysfibrinogenemia and multiple sclerosis: spuriously associated or causally linked?
Background: The inherited dysfibrinogenemias comprise rare congenital coagulation disorders which are clinically characterized by bleeding diathesis and, in occasional patients, by thrombotic tendency or combined bleeding-thrombotic events. In recent years, accumulating evidence suggested that fibri...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Hippokratia |
|---|---|
| Prif Awduron: | , , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
SOCIETY OF "FRIENDS OF HIPPOKRATIA JOURNAL"
2017
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5997019/ https://ncbi.nlm.nih.gov/pubmed/29904258 |
| Tagiau: |
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