Cerebral Infarct Associated With Factor V Leiden Mutation In A Boy With Hemophilia A

dc.contributor.author	Olcay, L
dc.contributor.author	Gurgey, A
dc.contributor.author	Topaloglu, H
dc.contributor.author	Altay, S
dc.contributor.author	Parlak, H
dc.contributor.author	Firat, M
dc.date.accessioned	2019-12-10T10:34:59Z
dc.date.available	2019-12-10T10:34:59Z
dc.date.issued	1997
dc.identifier.issn	0361-8609
dc.identifier.uri	https://doi.org/10.1002/(SICI)1096-8652(199711)56:3<189::AID-AJH11>3.3.CO;2-3
dc.identifier.uri	http://hdl.handle.net/11655/13819
dc.description.abstract	An 11-year-old boy with mild hemophilia A was admitted to our hospital because of focal convulsions, Magnetic resonance imaging showed an old occipital infarct. Protein C, S, antithrombin ill, anticardiolipin antibodies and fibrinogen were normal. Heterozygosity for factor V Leiden mutation was detected, We suggest that factor V Leiden mutation should be studied in hemophiliacs with thrombosis. (C) 1997 Wiley-Liss, Inc.
dc.language.iso	en
dc.publisher	Wiley-Liss
dc.relation.isversionof	10.1002/(SICI)1096-8652(199711)56:3<189::AID-AJH11>3.3.CO;2-3
dc.rights	info:eu-repo/semantics/openAccess
dc.subject	Hematology
dc.title	Cerebral Infarct Associated With Factor V Leiden Mutation In A Boy With Hemophilia A
dc.type	info:eu-repo/semantics/article
dc.relation.journal	American Journal Of Hematology
dc.contributor.department	Çocuk Sağlığı ve Hastalıkları
dc.identifier.volume	56
dc.identifier.issue	3
dc.identifier.startpage	189
dc.identifier.endpage	190
dc.description.index	WoS