A prospective cohort study on the absolute risks of venous thromboembolism and predictive value of screening asymptomatic relatives of patients with hereditary deficiencies of protein S, protein C or antithrombin.

Mahmoodi, B K; Brouwer, J-L P; Ten Kate, M K; Lijfering, W M; Veeger, N J G M; Mulder, A B; Kluin-Nelemans, H C; Van Der Meer, J

Mahmoodi, B K; Brouwer, J-L P; Ten Kate, M K; Lijfering, W M; Veeger, N J G M; Mulder, A B; Kluin-Nelemans, H C; Van Der Meer, J.

Affiliation

Mahmoodi BK; Division of Hemostasis and Thrombosis, Department of Hematology, University Medical Center, Groningen, the Netherlands. b.k.mahmoodi@int.umcg.nl

J Thromb Haemost ; 8(6): 1193-200, 2010 Jun.

Article in En | MEDLINE | ID: mdl-20230415

Subject(s)

Protein C Deficiency/genetics; Protein S Deficiency/genetics; Thrombophilia/genetics; Venous Thromboembolism/epidemiology; Humans; Prospective Studies; Risk Factors; Venous Thromboembolism/diagnosis

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Protein S Deficiency / Thrombophilia / Protein C Deficiency / Venous Thromboembolism Type of study: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limits: Humans Language: En Journal: J Thromb Haemost Journal subject: HEMATOLOGIA Year: 2010 Type: Article Affiliation country: Netherlands

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