Φορτώνει......
Genotype and phenotype correlation in intracranial hemorrhage in neonatal factor VII deficiency among Thai children
Congenital factor VII (FVII) deficiency is a rare inherited coagulopathy. The clinical manifestations and clinical findings vary widely, ranging from asymptomatic to life-threatening bleeding, including intracranial hemorrhage (ICH), with prolonged prothrombin time, normal partial thromboplastin tim...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Appl Clin Genet |
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| Κύριοι συγγραφείς: | , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Dove Medical Press
2017
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5484628/ https://ncbi.nlm.nih.gov/pubmed/28684918 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/TACG.S139788 |
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