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Hereditary thrombophilia
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Acquired factor VIII inhibitor in a pacient with antiphospholipid syndrome and hereditary thrombophilia
Publication without faculty affiliation
publication
Today's view of hereditary thrombophilia
2022 |
First Faculty of Medicine
publication
The impact of hereditary thrombophilia on the incidence of postoperative venous thromboembolism in colorectal cancer patients: aprospective cohort study: Hereditary thrombophilia and VTE in colorectal cancer surgery
2019 |
First Faculty of Medicine, Faculty of Physical Education and Sport
publication
The impact of hereditary thrombophilia on the incidence of postoperative venous thromboembolism in colorectal cancer patients: a prospective cohort study: Hereditary thrombophilia and VTE in colorectal cancer surgery
2019 |
First Faculty of Medicine
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Hereditary thrombophilias - which of them should be diagnosed using genetic tests?
2012 |
First Faculty of Medicine
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Is screening for hereditary thrombophilia indicated in first early pregnancy loss?
2012 |
First Faculty of Medicine
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Comment on article Does heparin prevent adverse pregnancy outcomes associated with hereditary thrombophilia?
2008 |
Publication without faculty affiliation
publication
Pharmacological prophalyxis and treatment of thromboembolism in patients with herteditary thrombophilic status
2019 |
First Faculty of Medicine
publication
The frequencies of six important thrombophilic mutations in a population of the Czech Republic
2014 |
First Faculty of Medicine
publication
Early pregnancy loss and inherited thrombophilic states.
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2009 |
Publication without faculty affiliation
publication
Genetically-conditioned risk factors for thrombophilia in GPs
2017 |
First Faculty of Medicine
publication
Multiple thrombophilia mutations as a possible cause of premature myocardial infarction
2017 |
First Faculty of Medicine
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Congenital and acquired thrombophilias
2021 |
First Faculty of Medicine
publication
Questions about prophylaxis and treatment of venous thromboembolism in 2006
2006 |
First Faculty of Medicine
publication
Analysis of risk factor : the rationale of the guildelines of the Czech Hematological Society for diagnosis and treatment of chronic myeloproliferative disorders with thrombocythemia
2006 |
First Faculty of Medicine
publication
Frequencies of the new thrombophilic mutations of antithrombin (SERPINC1) (IVS +141G>A), glycoprotein GPVI (Ser219Pro) and cytochrome CYP4V2 (Lys259Gln) in healthy middle-aged people in Central Bohemia
2012 |
First Faculty of Medicine
publication
Analysis of risk factors: The rationale of the guidelines of the Czech Hematological Society for diagnosis and treatment of chronic myeloproliferative disorders with thrombocythemia
2006 |
Second Faculty of Medicine
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Prevalence of thrombophilic mutations of FV Leiden, prothrombin G20210A and PAI-1 4G/5G and their combinations in a group of 1,450 healthy middle-aged individuals in the Prague and Central Bohemian regions (results of FRET real-time PCR assay)
2012 |
First Faculty of Medicine