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Molecular Review of Suspected Alport Syndrome Patients-A Single-Centre Experience.
Halat-Wolska P, Ciara E, Pac M, Obrycki Ł, Wicher D, Iwanicka-Pronicka K, Bielska E, Chałupczyńska B, Siestrzykowska D, Kostrzewa G, Stawiński P, Płoski R, Litwin M, Chrzanowska K. Halat-Wolska P, et al. Among authors: ciara e. Genes (Basel). 2025 Feb 4;16(2):196. doi: 10.3390/genes16020196. Genes (Basel). 2025. PMID: 40004525 Free PMC article.
Correction: Exome sequencing reveals IFT172 variants in patients with non-syndromic cholestatic liver disease.
Neřoldová M, Ciara E, Slatinská J, Fraňková S, Lišková P, Kotalová R, Globinovská J, Šafaříková M, Pfeiferová L, Zůnová H, Mrázová L, Stránecký V, Vrbacká A, Fabián O, Sticová E, Skanderová D, Šperl J, Kalousová M, Zima T, Macek M, Pawlowska J, Knisely AS, Kmoch S, Jirsa M. Neřoldová M, et al. Among authors: ciara e. PLoS One. 2025 Jan 30;20(1):e0318705. doi: 10.1371/journal.pone.0318705. eCollection 2025. PLoS One. 2025. PMID: 39883651 Free PMC article.
Clinical heterogeneity of polish patients with KAT6B-related disorder.
Klaniewska M, Bolanowska-Tyszko A, Latos-Bielenska A, Jezela-Stanek A, Szczaluba K, Krajewska-Walasek M, Ciara E, Pelc M, Jurkiewicz D, Stawinski P, Zubkiewicz-Kucharska A, Rydzanicz M, Ploski R, Smigiel R. Klaniewska M, et al. Among authors: ciara e. Mol Genet Genomic Med. 2023 Dec;11(12):e2265. doi: 10.1002/mgg3.2265. Epub 2023 Sep 1. Mol Genet Genomic Med. 2023. PMID: 37658610 Free PMC article.
110 results