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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2005 1
2007 2
2008 2
2009 1
2011 1
2012 1
2013 3
2016 2
2017 3
2019 1
2020 3
2021 3
2022 2
2024 0

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20 results

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Page 1
ALK alterations in salivary gland carcinomas.
Majewska H, Gorczyński A, Czapiewski P, Menon R, Mueller J, Lakis S, Heuckmann JM, Laco J, Gupta R, Andreasen S, Stodulski D, Iliszko M, Dziadziuszko R, Jassem J, Heukamp LC, Biernat W. Majewska H, et al. Among authors: iliszko m. Virchows Arch. 2021 May;478(5):933-941. doi: 10.1007/s00428-020-02971-w. Epub 2020 Nov 25. Virchows Arch. 2021. PMID: 33237469 Free PMC article.
Expression of BARD1 β Isoform in Selected Pediatric Tumors.
Jasiak A, Krawczyńska N, Iliszko M, Czarnota K, Buczkowski K, Stefanowicz J, Adamkiewicz-Drożyńska E, Cichosz G, Iżycka-Świeszewska E. Jasiak A, et al. Among authors: iliszko m. Genes (Basel). 2021 Jan 26;12(2):168. doi: 10.3390/genes12020168. Genes (Basel). 2021. PMID: 33530592 Free PMC article.
Bilateral Ovarian Germ Cell Tumor in a 46,XX Female with Nijmegen Breakage Syndrome and Hypergonadotropic Hypogonadism.
Krawczyk MA, Styczewska M, Birkholz-Walerzak D, Iliszko M, Lipska-Zietkiewicz BS, Kosiak W, Irga-Jaworska N, Izycka-Swieszewska E, Bien E. Krawczyk MA, et al. Among authors: iliszko m. J Clin Res Pediatr Endocrinol. 2022 Jun 7;14(2):251-257. doi: 10.4274/jcrpe.galenos.2021.2021.0151. Epub 2021 Sep 21. J Clin Res Pediatr Endocrinol. 2022. PMID: 34544220 Free PMC article.
Personalized health risk assessment based on single-cell RNA sequencing analysis of a male with 45, X/48, XYYY karyotype.
Koczkowska M, Jąkalski M, Birkholz-Walerzak D, Kostecka A, Iliszko M, Wójcik M, Lewandowski K, Milska-Musa K, Buckley PG, Drężek K, Juhas U, Kuziemska E, Maciejewska A, Pawłowski R, Wasąg B, Filipowicz N, Chojnowska K, Ławrynowicz U, Dumanski JP, Lipska-Ziętkiewicz BS, Mieczkowski J, Piotrowski A. Koczkowska M, et al. Among authors: iliszko m. Sci Rep. 2022 Dec 2;12(1):20854. doi: 10.1038/s41598-022-25308-w. Sci Rep. 2022. PMID: 36460769 Free PMC article.
Genomic findings in patients with clinical suspicion of 22q11.2 deletion syndrome.
Koczkowska M, Wierzba J, Śmigiel R, Sąsiadek M, Cabała M, Ślężak R, Iliszko M, Kardaś I, Limon J, Lipska-Ziętkiewicz BS. Koczkowska M, et al. Among authors: iliszko m. J Appl Genet. 2017 Feb;58(1):93-98. doi: 10.1007/s13353-016-0366-1. Epub 2016 Sep 14. J Appl Genet. 2017. PMID: 27629806 Free PMC article.
A girl with duplication 9q34 syndrome.
Gawlik-Kuklinska K, Iliszko M, Wozniak A, Debiec-Rychter M, Kardas I, Wierzba J, Limon J. Gawlik-Kuklinska K, et al. Among authors: iliszko m. Am J Med Genet A. 2007 Sep 1;143A(17):2019-23. doi: 10.1002/ajmg.a.31847. Am J Med Genet A. 2007. PMID: 17663474
20 results