Publication:
Intracranial Haemorrhage due to Factor V Deficiency

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dc.authorscopusid56450837600
dc.authorscopusid6701356032
dc.contributor.authorTotan, M.
dc.contributor.authorAlbayrak, D.
dc.date.accessioned2020-06-21T15:50:42Z
dc.date.available2020-06-21T15:50:42Z
dc.date.issued1999
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Totan] Mehmet, Dept. of Paediatric Haemutology, Ondokuz Mayis Üniversitesi, Samsun, Turkey, Department of Paediatric Haematology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Albayrak] Davut, Dept. of Paediatric Haemutology, Ondokuz Mayis Üniversitesi, Samsun, Turkeyen_US
dc.description.abstractFactor V deficiency is a rare coagulation disorder which is inherited autosomal recessively. Factor V deficiency should be considered in infants with bleeding disorders and prolonged prothrombin and activated partial thromboplastin times if bleeding continues in spite of vitamin K injection. In this article, the case of an infant with an intracranial haemorrhage due to congenital factor V deficiency is reported.en_US
dc.identifier.doi10.1080/08035259950170150
dc.identifier.endpage343en_US
dc.identifier.issn0803-5253
dc.identifier.issn1651-2227
dc.identifier.issue3en_US
dc.identifier.pmid10229050
dc.identifier.scopus2-s2.0-0033041974
dc.identifier.scopusqualityQ1
dc.identifier.startpage342en_US
dc.identifier.urihttps://doi.org/10.1080/08035259950170150
dc.identifier.volume88en_US
dc.identifier.wosWOS:000079338200021
dc.identifier.wosqualityQ2
dc.language.isoenen_US
dc.publisherWileyen_US
dc.relation.ispartofActa Paediatricaen_US
dc.relation.journalActa Paediatricaen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectFactor V Deficiencyen_US
dc.subjectIntracranial Haemorrhageen_US
dc.titleIntracranial Haemorrhage due to Factor V Deficiencyen_US
dc.typeArticleen_US
dspace.entity.typePublication

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