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The impact of PROS1 mutation position on thrombotic risk in protein S-deficient patients.
Res Pract Thromb Haemost. 2023 May 24;7(4):100194. doi: 10.1016/j.rpth.2023.100194. eCollection 2023 May.
Res Pract Thromb Haemost. 2023.
PMID: 37384225
Free PMC article.
Diagnosing Czech Patients with Inherited Platelet Disorders.
Louzil J, Stikarova J, Provaznikova D, Hrachovinova I, Fenclova T, Musil J, Radek M, Kaufmanova J, Geierova V, Ceznerova E, Salaj P, Kotlin R.
Louzil J, et al. Among authors: geierova v.
Int J Mol Sci. 2022 Nov 19;23(22):14386. doi: 10.3390/ijms232214386.
Int J Mol Sci. 2022.
PMID: 36430862
Free PMC article.
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Clinical manifestation and molecular genetic characterization of MYH9 disorders.
Provaznikova D, Geierova V, Kumstyrova T, Kotlin R, Mikulenkova D, Zurkova K, Matoska V, Hrachovinova I, Rittich S.
Provaznikova D, et al. Among authors: geierova v.
Platelets. 2009 Aug;20(5):289-96. doi: 10.1080/09537100902993022.
Platelets. 2009.
PMID: 19557653
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Identifying risk factors and optimizing standard of care for patients with acquired haemophilia A: Results from a Czech patient cohort.
Salaj P, Geierová V, Ivanová E, Loužil J, Pohlreichová V, Hrachovinová I, Dulíček P.
Salaj P, et al. Among authors: geierova v.
Haemophilia. 2020 Jul;26(4):643-651. doi: 10.1111/hae.14084. Epub 2020 Jun 26.
Haemophilia. 2020.
PMID: 32590889
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A novel natural mutation AαPhe98Ile in the fibrinogen coiled-coil affects fibrinogen function.
Riedelová-Reicheltová Z, Kotlín R, Suttnar J, Geierová V, Riedel T, Májek P, Dyr JE.
Riedelová-Reicheltová Z, et al. Among authors: geierova v.
Thromb Haemost. 2014 Jan;111(1):79-87. doi: 10.1160/TH13-04-0267. Epub 2013 Oct 10.
Thromb Haemost. 2014.
PMID: 24108601
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Economic analysis of recombinant activated factor VII versus plasma-derived activated prothrombin complex concentrate in mild to moderate bleeds: haemophilia registry data from the Czech Republic.
Salaj P, Penka M, Smejkal P, Geierova V, Ovesná P, Brabec P, Cetkovsky P, Kubes R, Mesterton J, Lindgren P.
Salaj P, et al. Among authors: geierova v.
Thromb Res. 2012 May;129(5):e233-7. doi: 10.1016/j.thromres.2012.02.005. Epub 2012 Mar 2.
Thromb Res. 2012.
PMID: 22386136
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Abnormal fibrinogen Zlín (γThr21Ile) with missense mutation causing hypofibrinogenemia.
Riedelová-Reicheltová Z, Riedel T, Májek P, Kotlin R, Geierová V, Suttnar J, Dyr JE.
Riedelová-Reicheltová Z, et al. Among authors: geierova v.
Acta Haematol. 2014;132(2):140-3. doi: 10.1159/000356781.
Acta Haematol. 2014.
PMID: 24556703
No abstract available.
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