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Distinct characteristics of multisystem inflammatory syndrome in children in Poland.
Ludwikowska KM, Okarska-Napierała M, Dudek N, Tracewski P, Kusa J, Piwoński KP, Afelt A, Cysewski D, Biela M, Werner B, Jackowska T, Suski-Grabowski C, Kursa MB, Kuchar E, Szenborn L; MOIS CoR Study Group. Ludwikowska KM, et al. Among authors: biela m. Sci Rep. 2021 Dec 7;11(1):23562. doi: 10.1038/s41598-021-02669-2. Sci Rep. 2021. PMID: 34876594 Free PMC article.
COVID-19 mRNA BNT162b2 vaccine immunogenicity among children with a history of paediatric multisystem inflammatory syndrome temporally associated with COVID-19 (PIMS-TS).
Ludwikowska KM, Popiel A, Matkowska-Kocjan A, Biela M, Wójcik M, Szenborn F, Wielgos K, Pielka-Markiewicz E, Zaryczański J, Kursa MB, Szenborn L. Ludwikowska KM, et al. Among authors: biela m. Vaccine. 2023 May 16;41(21):3317-3327. doi: 10.1016/j.vaccine.2023.04.035. Epub 2023 Apr 14. Vaccine. 2023. PMID: 37087396 Free PMC article.
COVID-19 mRNA BNT162b2 vaccine safety and B-cell and T-cell reactogenicity among children with a history of paediatric multisystem inflammatory syndrome temporally associated with COVID-19 (PIMS-TS) - preliminary study.
Ludwikowska KM, Popiel A, Matkowska-Kocjan A, Olbromski MJ, Biela M, Wójcik M, Szenborn F, Wielgos K, Pielka-Markiewicz E, Zaryczański J, Kursa MB, Szenborn L. Ludwikowska KM, et al. Among authors: biela m. Vaccine. 2023 Mar 24;41(13):2289-2299. doi: 10.1016/j.vaccine.2023.02.072. Epub 2023 Mar 2. Vaccine. 2023. PMID: 36870876 Free PMC article.
Single median maxillary central incisor syndrome and variant in SMO gene associated with SHH pathway.
Zatoński T, Pazdro-Zastawny K, Morawska-Kochman M, Biela M, Kołtowska A, Rydzanicz M, Rozensztrauch A, Kosińska J, Dorobisz K, Płoski R, Śmigiel R. Zatoński T, et al. Among authors: biela m. Int J Pediatr Otorhinolaryngol. 2020 Jul;134:110038. doi: 10.1016/j.ijporl.2020.110038. Epub 2020 Apr 13. Int J Pediatr Otorhinolaryngol. 2020. PMID: 32335464
Rapid Whole-Exome Sequencing as a Diagnostic Tool in a Neonatal/Pediatric Intensive Care Unit.
Śmigiel R, Biela M, Szmyd K, Błoch M, Szmida E, Skiba P, Walczak A, Gasperowicz P, Kosińska J, Rydzanicz M, Stawiński P, Biernacka A, Zielińska M, Gołębiowski W, Jalowska A, Ohia G, Głowska B, Walas W, Królak-Olejnik B, Krajewski P, Sykut-Cegielska J, Sąsiadek MM, Płoski R. Śmigiel R, et al. Among authors: biela m. J Clin Med. 2020 Jul 13;9(7):2220. doi: 10.3390/jcm9072220. J Clin Med. 2020. PMID: 32668698 Free PMC article.
Variants of ATP1A3 in residue 756 cause a separate phenotype of relapsing encephalopathy with cerebellar ataxia (RECA)-Report of two cases and literature review.
Biela M, Rydzanicz M, Szymanska K, Pieniawska-Smiech K, Lewandowicz-Uszynska A, Chruszcz J, Benben L, Kuzior-Plawiak M, Szyld P, Jakubiak A, Szenborn L, Ploski R, Smigiel R. Biela M, et al. Mol Genet Genomic Med. 2021 Sep;9(9):e1772. doi: 10.1002/mgg3.1772. Epub 2021 Aug 2. Mol Genet Genomic Med. 2021. PMID: 34342181 Free PMC article. Review.
37 results