Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Sandra Ohlenforst"'
Autor:
Barbara Preisler, Behnaz Pezeshkpoor, Anja Merzenich, Sandra Ohlenforst, Heiko Rühl, Vytautas Ivaškevičius, Ute Scholz, Hagen Bönigk, Wolfgang Eberl, Barbara Zieger, Anna Pavlova, Johannes Oldenburg
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 4, p 2384 (2024)
Congenital factor VII (FVII) deficiency is a rare genetic bleeding disorder characterized by deficient or reduced activity of coagulation FVII. It is caused by genetic variants in the F7 gene. We aimed to evaluate the rate of detection of pathogenic
Externí odkaz:
https://doaj.org/article/2b277c9610dd4be19f21749ffa1e7139
Autor:
Barbara Preisler, Behnaz Pezeshkpoor, Jutta Beckedahl, Sandra Ohlenforst, Heiko Rühl, Ute Scholz, Hagen Bönigk, Wolfgang Eberl, Barbara Zieger, Anna Pavlova, Johannes Oldenburg
Publikováno v:
52. Hamburger Hämophilie Symposion.
Autor:
Arijit Biswas, H. P. Kohler, Sandra Ohlenforst, Vytautas Ivaskevicius, Manuela Krause, Inge Scharrer, Verena Schroeder, Johannes Oldenburg, Hannelore Rott, Ralph M. Loreth
Publikováno v:
Haemophilia.
Severe factor XIII (FXIII) deficiency is a rare autosomal recessive coagulation disorder affecting one in two million individuals. The aim of the present study was to screen for and analyse F13B gene defects in the German population. A total of 150 p
Publikováno v:
International Journal of Cardiology. 114:380-381
Patients with inherited thrombophilia are at high risk for the development of venous thrombosis that manifests mainly as deep venous thrombosis of the legs and/or pulmonary embolism. We report spontaneous right-sided intracardiac thrombosis in a youn