| dc.contributor.author | Totan, M | |
| dc.contributor.author | Albayrak, D | |
| dc.date.accessioned | 2020-06-21T15:50:42Z | |
| dc.date.available | 2020-06-21T15:50:42Z | |
| dc.date.issued | 1999 | |
| dc.identifier.issn | 0803-5253 | |
| dc.identifier.issn | 1651-2227 | |
| dc.identifier.uri | https://doi.org/10.1080/08035259950170150 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12712/22444 | |
| dc.description | WOS: 000079338200021 | en_US |
| dc.description | PubMed: 10229050 | en_US |
| dc.description.abstract | Factor 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.language.iso | eng | en_US |
| dc.publisher | Wiley | en_US |
| dc.relation.isversionof | 10.1080/08035259950170150 | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.subject | factor V deficiency | en_US |
| dc.subject | intracranial haemorrhage | en_US |
| dc.title | Intracranial haemorrhage due to factor V deficiency | en_US |
| dc.type | article | en_US |
| dc.contributor.department | OMÜ | en_US |
| dc.identifier.volume | 88 | en_US |
| dc.identifier.issue | 3 | en_US |
| dc.identifier.startpage | 342 | en_US |
| dc.identifier.endpage | 343 | en_US |
| dc.relation.journal | Acta Paediatrica | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
