MUDr. Petr Smejkal, Ph.D.
Assistant professor, Department of Laboratory Methods
correspondence Address:
Kamenice 753/5, 625 00 Brno
phone: | +420 532 23 3188 |
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e‑mail: |
social and academic networks: |
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Total number of publications: 74
2024
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Factor IX activity measurement of recombinant FIX Fc fusion protein eftrenonacog alfa with one-stage clotting and chromogenic substrate assay
Year: 2024, type: Conference abstract
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Impact of thrombocytopenia-associated c.-118C>T and c.-140C>G ANKRD26 5’UTR variants in three-generational pedigree
Platelets, year: 2024, volume: 35, edition: 1, DOI
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Prospective examination of acquired von Willebrand syndrome co-occurrence in patients with BCR-ABL1-negative myeloproliferative neoplasms
Year: 2024, type: Conference abstract
2023
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Analýza variant genu ANKRD 26 v 5´ nepřekládané oblasti u kohorty pacientů s podezřením na dědičné hematologické onemocnění.
Year: 2023, type: Conference abstract
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Bleeding pattern and consumption of factor VIII concentrate in adult patients with haemophilia A without inhibitors in the Czech Republic between 2013 and 2021 (Czech National Haemophilia Programme registry data)
Annals of hematology, year: 2023, volume: 102, edition: 11, DOI
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rFVIIIFc v léčbě hemofilie A z pohledu reálné klinické praxe tří center pro léčbu hemofilie v České republice
Transfuze a Hematologie dnes, year: 2023, volume: 29, edition: 2, DOI
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Role trombelastografie v diagnostice poruch hemostázy u jaterních onemocnění
Year: 2023, type: Appeared in Conference without Proceedings
2022
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A GP1BA Variant in a Czech Family with Monoallelic Bernard-Soulier Syndrome
International Journal of Molecular Sciences, year: 2022, volume: 23, edition: 2, DOI
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Analysis of ANKRD26 gene 5´UTR variant in a cohort of Czech patients with suspected hereditary hematological disorder
Year: 2022, type: Conference abstract
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ANALYSIS OF ANKRD26 GENE 5'UTR VARIANTS IN A COHORT OF CZECH PATIENTS WITH SUSPECTED HEREDITARY HEMATOLOGICAL DISORDER
Year: 2022, type: Conference abstract