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Ceska Gynekologie|June 25, 2021
Hereditary antithrombin deficiency in pregnancy - severe thrombophilic disorder as a danger for mother and foetusIrena Čápová, Peter Salaj, Ingrid HrachovinováJournal of Perinatal Medicine|September 13, 2006
Randomized prospective comparative study of ursodeoxycholic acid and S-adenosyl-L-methionine in the treatment of intrahepatic cholestasis of pregnancyTomás Binder, Peter Salaj, Tomás Zima, et al.European Journal of Haematology|November 21, 2008
Patients with acute coronary syndromes have low tissue factor activity and microparticle count, but normal concentration of tissue factor antigen in platelet free plasma: a pilot studyMartin Maly, Ingrid Hrachovinova, Pavol Tomasov, et al.Biomedical Papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia|November 7, 2012
Does asymptomatic carriage of FV Leiden and FII prothrombin mutations in heterozygous configuration pose an increased risk of thrombembolic complications in the course of pregnancy, labor and puerperium?Blanka Vavrinkova, Tomas Binder, Ivana Hadacova, et al.Platelets|October 18, 2008
High-resolution melting analysis for detection of MYH9 mutationsDana Provaznikova, Tereza Kumstyrova, Roman Kotlin, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|June 27, 2020
Identifying risk factors and optimizing standard of care for patients with acquired haemophilia A: Results from a Czech patient cohortPeter Salaj, Vera Geierová, Eva Ivanová, et al.Thrombosis Research|December 11, 2013
Economic evaluation of rFVIIa high initial dose compared to rFVIIa standard initial dose in patients with haemophilia with inhibitors using the Czech HemoRec registryPeter Salaj, Radovan Kubes, Petr Cetkovsky, et al.European Journal of Haematology|March 3, 2007
A novel fibrinogen variant--Praha I: hypofibrinogenemia associated with gamma Gly351Ser substitutionRoman Kotlín, Martina Chytilová, Jirí Suttnar, et al.European Journal of Haematology|May 20, 2008
A novel fibrinogen variant--Liberec: dysfibrinogenaemia associated with gamma Tyr262Cys substitutionRoman Kotlín, Alzbeta Sobotková, Jirí Suttnar, et al.Pageof 3