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jan louzir
(64 results)?
Diagnosing Czech Patients with Inherited Platelet Disorders.
Int J Mol Sci. 2022 Nov 19;23(22):14386. doi: 10.3390/ijms232214386.
Int J Mol Sci. 2022.
PMID: 36430862
Free PMC article.
Thrombosis-associated hypofibrinogenemia: novel abnormal fibrinogen variant FGG c.8G>A with oxidative posttranslational modifications.
Ceznerová E, Kaufmanová J, Stikarová J, Pastva O, Loužil J, Chrastinová L, Suttnar J, Kotlín R, Dyr JE.
Ceznerová E, et al. Among authors: louzil j.
Blood Coagul Fibrinolysis. 2022 Jun 1;33(4):228-237. doi: 10.1097/MBC.0000000000001125. Epub 2022 Jan 21.
Blood Coagul Fibrinolysis. 2022.
PMID: 35067535
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Predicting the development of hemophilic arthropathy in patients with hemophilia based on patient age: a retrospective single-center database study.
Kubeš R, Stollin M, Magersky Š, Bobelyak M, Vaculík J, Včelák J, Antonín Kuběna A, Loužil J, Salaj P.
Kubeš R, et al. Among authors: louzil j.
Expert Rev Hematol. 2023 Jul-Dec;16(12):1099-1105. doi: 10.1080/17474086.2023.2289536. Epub 2023 Dec 18.
Expert Rev Hematol. 2023.
PMID: 38015035
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Structural and Functional Characterization of Four Novel Fibrinogen Mutations in FGB Causing Congenital Fibrinogen Disorder.
Ceznerová E, Kaufmanová J, Sovová Ž, Štikarová J, Loužil J, Kotlín R, Suttnar J.
Ceznerová E, et al. Among authors: louzil j.
Int J Mol Sci. 2022 Jan 10;23(2):721. doi: 10.3390/ijms23020721.
Int J Mol Sci. 2022.
PMID: 35054908
Free PMC article.
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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: louzil j.
Haemophilia. 2020 Jul;26(4):643-651. doi: 10.1111/hae.14084. Epub 2020 Jun 26.
Haemophilia. 2020.
PMID: 32590889
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