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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...

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Détails bibliographiques
Publié dans:Hippokratia
Auteurs principaux: Kimiskidis, VK, Papadakis, E, Papaliagkas, V, Papagiannopoulos, S, Galanakis, DK
Format: Artigo
Langue:Inglês
Publié: SOCIETY OF "FRIENDS OF HIPPOKRATIA JOURNAL" 2017
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC5997019/
https://ncbi.nlm.nih.gov/pubmed/29904258
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