Rare congenital bleeding disorders

The rare congenital bleeding disorders are a heterogeneous group of diseases which include deficiencies of fibrinogen, prothrombin and factors V, V + VIII, VII, X, XI and XIII. They are usually transmitted as autosomal recessive disorders, and the prevalence of the severe forms ranges from one case...

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Guardat en:
Dades bibliogràfiques
Publicat a:Ann Transl Med
Autors principals: Franchini, Massimo, Marano, Giuseppe, Pupella, Simonetta, Vaglio, Stefania, Masiello, Francesca, Veropalumbo, Eva, Piccinini, Vanessa, Pati, Ilaria, Catalano, Liviana, Liumbruno, Giancarlo Maria
Format: Artigo
Idioma:Inglês
Publicat: AME Publishing Company 2018
Matèries:
Review Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6174186/
https://ncbi.nlm.nih.gov/pubmed/30306070
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21037/atm.2018.08.34
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