Budd-Chiari syndrome in a paroxysmal nocturnal hemoglobinuria patient with coexistence of factor II and MTHFR mutations.

Shamseddine, A I; Otrock, Z K; Mahfouz, R A R; Makarem, J A; Taher, A T

Shamseddine, A I; Otrock, Z K; Mahfouz, R A R; Makarem, J A; Taher, A T.

J Thromb Haemost ; 3(5): 1111, 2005 May.

Article in En | MEDLINE | ID: mdl-15869626

Subject(s)

Budd-Chiari Syndrome/diagnosis; Hemoglobinuria, Paroxysmal/complications; Hemoglobinuria/complications; Methylenetetrahydrofolate Dehydrogenase (NAD+)/genetics; Mutation; Adult; Ascites; Factor V/genetics; Hemoglobinuria/diagnosis; Hemoglobinuria, Paroxysmal/diagnosis; Heterozygote; Humans; International Normalized Ratio; Male; Prothrombin/genetics; Spleen/diagnostic imaging; Thrombophilia; Time Factors; Tomography, X-Ray Computed; Warfarin/pharmacology

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Collection: 01-internacional Database: MEDLINE Main subject: Methylenetetrahydrofolate Dehydrogenase (NAD/) / Hemoglobinuria / Hemoglobinuria, Paroxysmal / Budd-Chiari Syndrome / Mutation Type of study: Diagnostic_studies Limits: Adult / Humans / Male Language: En Journal: J Thromb Haemost Journal subject: HEMATOLOGIA Year: 2005 Type: Article

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