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Page 1
Serum microRNA in patients undergoing atrial fibrillation ablation.
Sci Rep. 2020 Mar 10;10(1):4424. doi: 10.1038/s41598-020-61322-6.
Sci Rep. 2020.
PMID: 32157193
Free PMC article.
A novel microRNA differentially expressed in patients with persistent and paroxysmal atrial fibrillation.
Góra M, Kiliszek M, Maciak K, Salamaga H, Łazowski K, Burzyńska B.
Góra M, et al. Among authors: maciak k.
Pol Arch Intern Med. 2024 Jan 29;134(1):16650. doi: 10.20452/pamw.16650. Epub 2023 Dec 22.
Pol Arch Intern Med. 2024.
PMID: 38133883
Free article.
No abstract available.
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Expression of versican mRNA transcript to predict cardiac remodelling after myocardial infarction.
Chabior A, Gąsecka A, Marchel M, Gozdowska R, Makowska A, Maciak K, Góra M, Filipiak KJ, Burzyńska B, Opolski G.
Chabior A, et al. Among authors: maciak k.
Kardiol Pol. 2021;79(7-8):833-840. doi: 10.33963/KP.a2021.0042. Epub 2021 Jun 24.
Kardiol Pol. 2021.
PMID: 34166520
Free article.
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Changes in MicroRNA Expression during Rabbit Hemorrhagic Disease Virus (RHDV) Infection.
Hukowska-Szematowicz B, Maciejak-Jastrzębska A, Blatkiewicz M, Maciak K, Góra M, Janiszewska J, Burzyńska B.
Hukowska-Szematowicz B, et al. Among authors: maciak k.
Viruses. 2020 Aug 31;12(9):965. doi: 10.3390/v12090965.
Viruses. 2020.
PMID: 32878241
Free PMC article.
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PKLR mutations in pyruvate kinase deficient Polish patients: Functional characteristics of c.101-1G > A and c.1058delAAG variants.
Maciak K, Jurkiewicz A, Strojny W, Adamowicz-Salach A, Romiszewska M, Jackowska T, Kwiecinska K, Poznanski J, Gora M, Burzynska B.
Maciak K, et al.
Blood Cells Mol Dis. 2024 Mar 26;107:102841. doi: 10.1016/j.bcmd.2024.102841. Online ahead of print.
Blood Cells Mol Dis. 2024.
PMID: 38581917
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A Family Affected by a Life-Threatening Erythrocyte Defect Caused by Pyruvate Kinase Deficiency With Normal Iron Status: A Case Report.
Maciak K, Adamowicz-Salach A, Poznanski J, Gora M, Fronk J, Burzynska B.
Maciak K, et al.
Front Genet. 2020 Oct 28;11:560248. doi: 10.3389/fgene.2020.560248. eCollection 2020.
Front Genet. 2020.
PMID: 33193643
Free PMC article.
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Hereditary xerocytosis - spectrum and clinical manifestations of variants in the PIEZO1 gene, including co-occurrence with a novel β-globin mutation.
Maciak K, Adamowicz-Salach A, Siwicka A, Poznanski J, Urasinski T, Plochocka D, Gora M, Burzynska B.
Maciak K, et al.
Blood Cells Mol Dis. 2020 Feb;80:102378. doi: 10.1016/j.bcmd.2019.102378. Epub 2019 Oct 22.
Blood Cells Mol Dis. 2020.
PMID: 31670187
Free article.
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