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Thrombosis Research|January 26, 2015
Molecular characterization of p.Asp77Gly and the novel p.Ala163Val and p.Ala163Glu mutations causing protein C deficiencyKitti B Kovács, István Pataki, Helga Bárdos, et al.
Orvosi Hetilap|August 16, 2002
[Frequency of hyperhomocysteinemia in hemodialysis patients with folic acid supplementation]István Kárpáti, József Balla, Gabriella Szóke, et al.
Scientific Reports|May 18, 2018
Low factor XIII levels after intravenous thrombolysis predict short-term mortality in ischemic stroke patientsEdina Gabriella Székely, Katalin Réka Czuriga-Kovács, Zsuzsanna Bereczky, et al.
Thrombosis Journal|November 13, 2025
Exploring factor XIII genetic diversity: a familial approach to inheritance and variationArshi Naz, Sana Zameer, Hyder Ali Pehilwani Rind, et al.
Journal of Translational Medicine|March 17, 2016
The lack of aspirin resistance in patients with coronary artery diseaseNóra Homoródi, Emese G Kovács, Sarolta Leé, et al.
Thrombosis Research|November 21, 2017
Clinical and laboratory characteristics of antithrombin deficiencies: A large cohort study from a single diagnostic centerRéka Gindele, Anna Selmeczi, Zsolt Oláh, et al.
International Journal of Molecular Sciences|December 1, 2019
Cellular Factor XIII, a Transglutaminase in Human Corneal KeratocytesZsuzsanna Z Orosz, Helga Bárdos, Amir H Shemirani, et al.
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