Coincidence of factor V Leiden mutation and a mutation in the prothrombin gene at position 20210 in a patient with puerperal cerebral venous thrombosis.

Weih, M; Mehraein, S; Valdueza, J M; Einhäupl, K M; Vetter, B; Kulozik, A E

Weih, M; Mehraein, S; Valdueza, J M; Einhäupl, K M; Vetter, B; Kulozik, A E.

Stroke ; 29(8): 1739-40, 1998 Aug.

Article in En | MEDLINE | ID: mdl-9707222

Subject(s)

Cerebrovascular Disorders/genetics; Factor V/genetics; Intracranial Embolism and Thrombosis/genetics; Point Mutation; Prothrombin/genetics; Adult; Cerebrovascular Disorders/etiology; Female; Humans; Intracranial Embolism and Thrombosis/complications; Postpartum Period

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Collection: 01-internacional Database: MEDLINE Main subject: Factor V / Prothrombin / Intracranial Embolism and Thrombosis / Cerebrovascular Disorders / Point Mutation Type of study: Etiology_studies Limits: Adult / Female / Humans Language: En Journal: Stroke Year: 1998 Document type: Article Country of publication: United States

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