Idiopathic Budd-Chiari syndrome in a patient with homozygous Factor V Leiden and heterozygous Factor II G20210A mutations. | Thromb Res;100(6): 567-8, 2000 Dec 15. | MEDLINE

Main content 1 Search 2 Footer 3

+A A -A High contrast

VHL Regional Portal

Information and Knowledge for Health

Subject descriptor lookup Advanced Search EVID@Easy

Idiopathic Budd-Chiari syndrome in a patient with homozygous Factor V Leiden and heterozygous Factor II G20210A mutations.

De Stefano, V; Madonna, P; Giannino, A; Coppola, A; Cerbone, A M; Pauciullo, P; Di Minno, G.

Thromb Res ; 100(6): 567-8, 2000 Dec 15.

Article in En | MEDLINE | ID: mdl-11197916

Subject(s)

Budd-Chiari Syndrome/genetics; Factor V/genetics; Prothrombin/genetics; Adult; Budd-Chiari Syndrome/blood; Budd-Chiari Syndrome/etiology; DNA Mutational Analysis; Heterozygote; Homozygote; Humans; Male; Point Mutation; Risk Factors; Thrombophilia/blood; Thrombophilia/genetics

Search on Google

Collection: 01-internacional Database: MEDLINE Main subject: Factor V / Prothrombin / Budd-Chiari Syndrome Type of study: Etiology_studies Limits: Adult / Humans / Male Language: En Journal: Thromb Res Year: 2000 Document type: Article Country of publication: United States

Search on Google

Collection: 01-internacional Database: MEDLINE Main subject: Factor V / Prothrombin / Budd-Chiari Syndrome Type of study: Etiology_studies Limits: Adult / Humans / Male Language: En Journal: Thromb Res Year: 2000 Document type: Article Country of publication: United States