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Andreas Stümpflen
Researcher at University of Vienna
Publications - 20
Citations - 1600
Andreas Stümpflen is an academic researcher from University of Vienna. The author has contributed to research in topics: Heart disease & Risk factor. The author has an hindex of 16, co-authored 20 publications receiving 1570 citations.
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Journal ArticleDOI
Effect of detailed fetal echocardiography as part of routine prenatal ultrasonographic screening on detection of congenital heart disease
TL;DR: Inclusion of detailed fetal echocardiography as a screening examination has a substantial effect on detection of congenital heart disease since a major proportion of prenatally detectable cases occur in a low-risk population.
Journal ArticleDOI
Hyperhomocysteinemia Is a Risk Factor of Recurrent Venous Thromboembolism
S. Eichinger,Andreas Stümpflen,Mirko Hirschl,Christine Bialonczyk,Kurt R. Herkner,Milena Stain,Barbara Schneider,Ingrid Pabinger,Klaus Lechner,Paul A. Kyrle +9 more
TL;DR: The high prevalence of hyperhomocysteinemia in thrombosis patients together with the increased risk of recurrence warrants extended patient screening and the impact on the risk ofRecurrence of prolonged anticoagulation, supplementation of folate and vitamin B12, or both have to be investigated.
Journal ArticleDOI
The risk of recurrent venous thromboembolism in patients with and without factor V Leiden
S. Eichinger,Ingrid Pabinger,Andreas Stümpflen,Mirko Hirschl,Christine Bialonczyk,Barbara Schneider,Christine Mannhalter,Erich Minar,Klaus Lechner,Paul A. Kyrle +9 more
TL;DR: Balancing the risk of recurrent VTE and bleeding from oral anticoagulants, patients with factor V Leiden are not likely to benefit from oral anti-coagulant therapy extended beyond six months.
Journal ArticleDOI
Clinical Studies and Thrombin Generation in Patients Homozygous or Heterozygous for the G20210A Mutation in the Prothrombin Gene
Paul A. Kyrle,Christine Mannhalter,Suzette Beguin,Andreas Stümpflen,Mirko Hirschl,Ansgar Weltermann,Milena Stain,Brigitte Brenner,Wolfgang Speiser,Ingrid Pabinger,Klaus Lechner,Sabine Eichinger +11 more
TL;DR: Hobbitosity for the G20210A mutation in the prothrombin gene is associated with a severe, albeit more benign, thrombotic diathesis compared with homozygosity for deficiencies of antithrombin, protein C, or protein S.
Journal ArticleDOI
The Risk of Early Recurrent Venous Thromboembolism after Oral Anticoagulant Therapy in Patients with the G20210A Transition in the Prothrombin Gene
S. Eichinger,Erich Minar,Mirko Hirschl,Christine Bialonczyk,Milena Stain,Christine Mannhalter,Andreas Stümpflen,Barbara Schneider,Klaus Lechner,Paul A. Kyrle +9 more
TL;DR: The risk of early recurrent venous thromboembolism is not higher in patients with the G20210A mutation than in those without the mutation, and long-term secondary thromboprophylaxis with oral anticoagulants in heterozygous carriers of the 20210A allele is not justified.