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Clinical features, etiology, and survival in patients with restrictive cardiomyopathy: A single-center experience.
Szczygieł JA, Michałek P, Truszkowska G, Drozd-Sokołowska J, Wróbel A, Franaszczyk M, Gawor-Prokopczyk M, Mazurkiewicz Ł, Ziarkiewicz M, Waszczuk-Gajda A, Legatowicz-Koprowska M, Walczak E, Stawiński P, Lutyńska A, Płoski R, Jędrzejczak WW, Bilińska ZT, Grzybowski J. Szczygieł JA, et al. Among authors: stawinski p. Kardiol Pol. 2023;81(12):1227-1236. doi: 10.33963/v.kp.97879. Epub 2023 Nov 8. Kardiol Pol. 2023. PMID: 37937352 Free article.
Cardiovascular involvement and prognosis in Loeys-Dietz syndrome.
Chmielewski P, Ponińska JK, Michalak E, Michałowska I, Kowalik I, Truszkowska G, Kugaudo M, Minota I, Stawiński P, Płoski R, Bilińska ZT. Chmielewski P, et al. Among authors: stawinski p. Kardiol Pol. 2023;81(11):1096-1102. doi: 10.33963/v.kp.97390. Epub 2023 Oct 12. Kardiol Pol. 2023. PMID: 37823753 Free 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: stawinski p. 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.
Barrett's Esophagus: An Updated Review.
Stawinski PM, Dziadkowiec KN, Kuo LA, Echavarria J, Saligram S. Stawinski PM, et al. Diagnostics (Basel). 2023 Jan 16;13(2):321. doi: 10.3390/diagnostics13020321. Diagnostics (Basel). 2023. PMID: 36673131 Free PMC article. Review.
Identification of New Copy Number Variation and the Evaluation of a CNV Detection Tool for NGS Panel Data in Polish Familial Hypercholesterolemia Patients.
Rutkowska L, Pinkier I, Sałacińska K, Kępczyński Ł, Salachna D, Lewek J, Banach M, Matusik P, Starostecka E, Lewiński A, Płoski R, Stawiński P, Gach A. Rutkowska L, et al. Among authors: stawinski p. Genes (Basel). 2022 Aug 10;13(8):1424. doi: 10.3390/genes13081424. Genes (Basel). 2022. PMID: 36011335 Free PMC article.
Prenatal Diagnosis of Jeune Syndrome Caused by Compound Heterozygous Variants in DYNC2H1 Gene-Case Report with Rapid WES Procedure and Differential Diagnosis of Lethal Skeletal Dysplasias.
Stembalska A, Rydzanicz M, Klaniewska M, Dudarewicz L, Pollak A, Biela M, Stawinski P, Ploski R, Smigiel R. Stembalska A, et al. Among authors: stawinski p. Genes (Basel). 2022 Jul 27;13(8):1339. doi: 10.3390/genes13081339. Genes (Basel). 2022. PMID: 35893076 Free PMC article.
Tracking Clonal Evolution of Multiple Myeloma Using Targeted Next-Generation DNA Sequencing.
Salomon-Perzyński A, Barankiewicz J, Machnicki M, Misiewicz-Krzemińska I, Pawlak M, Radomska S, Krzywdzińska A, Bluszcz A, Stawiński P, Rydzanicz M, Jakacka N, Solarska I, Borg K, Spyra-Górny Z, Szpila T, Puła B, Grosicki S, Stokłosa T, Płoski R, Lech-Marańda E, Jakubikova J, Jamroziak K. Salomon-Perzyński A, et al. Among authors: stawinski p. Biomedicines. 2022 Jul 12;10(7):1674. doi: 10.3390/biomedicines10071674. Biomedicines. 2022. PMID: 35884979 Free PMC article.
82 results