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

Year Number of Results
2002 2
2004 2
2005 6
2006 1
2007 2
2008 8
2009 9
2010 4
2011 8
2012 6
2013 4
2014 1
2015 5
2016 16
2017 18
2018 22
2019 20
2020 24
2021 28
2022 14
2023 14
2024 4

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186 results

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Page 1
New perspective in diagnostics of mitochondrial disorders: two years' experience with whole-exome sequencing at a national paediatric centre.
Pronicka E, Piekutowska-Abramczuk D, Ciara E, Trubicka J, Rokicki D, Karkucińska-Więckowska A, Pajdowska M, Jurkiewicz E, Halat P, Kosińska J, Pollak A, Rydzanicz M, Stawinski P, Pronicki M, Krajewska-Walasek M, Płoski R. Pronicka E, et al. Among authors: rydzanicz m. J Transl Med. 2016 Jun 12;14(1):174. doi: 10.1186/s12967-016-0930-9. J Transl Med. 2016. PMID: 27290639 Free PMC article.
Metagenomic search of viral coinfections in herpes simplex encephalitis patients.
Perlejewski K, Radkowski M, Rydzanicz M, Dzieciątkowski T, Silling S, Wieczorek M, Makowiecki M, Horban A, Laskus T. Perlejewski K, et al. Among authors: rydzanicz m. J Neurovirol. 2023 Oct;29(5):588-597. doi: 10.1007/s13365-023-01157-9. Epub 2023 Jul 25. J Neurovirol. 2023. PMID: 37490185 Free PMC article.
[Myopia in systemic disorders].
Mrugacz M, Rydzanicz M, Frajdenberg A, Podfigurna-Musielak M, Gajecka M. Mrugacz M, et al. Among authors: rydzanicz m. Klin Oczna. 2009;111(1-3):84-8. Klin Oczna. 2009. PMID: 19517854 Review. Polish.
TCEAL1 loss-of-function results in an X-linked dominant neurodevelopmental syndrome and drives the neurological disease trait in Xq22.2 deletions.
Hijazi H, Reis LM, Pehlivan D, Bernstein JA, Muriello M, Syverson E, Bonner D, Estiar MA, Gan-Or Z, Rouleau GA, Lyulcheva E, Greenhalgh L, Tessarech M, Colin E, Guichet A, Bonneau D, van Jaarsveld RH, Lachmeijer AMA, Ruaud L, Levy J, Tabet AC, Ploski R, Rydzanicz M, Kępczyński Ł, Połatyńska K, Li Y, Fatih JM, Marafi D, Rosenfeld JA, Coban-Akdemir Z, Bi W, Gibbs RA, Hobson GM, Hunter JV, Carvalho CMB, Posey JE, Semina EV, Lupski JR. Hijazi H, et al. Among authors: rydzanicz m. Am J Hum Genet. 2022 Dec 1;109(12):2270-2282. doi: 10.1016/j.ajhg.2022.10.007. Epub 2022 Nov 10. Am J Hum Genet. 2022. PMID: 36368327 Free PMC article.
Prenatal Detection of a FOXF1 Deletion in a Fetus with ACDMPV and Hydronephrosis.
Bzdęga K, Kutkowska-Kaźmierczak A, Deutsch GH, Plaskota I, Smyk M, Niemiec M, Barczyk A, Obersztyn E, Modzelewski J, Lipska I, Stankiewicz P, Gajecka M, Rydzanicz M, Płoski R, Szczapa T, Karolak JA. Bzdęga K, et al. Among authors: rydzanicz m. Genes (Basel). 2023 Feb 23;14(3):563. doi: 10.3390/genes14030563. Genes (Basel). 2023. PMID: 36980834 Free PMC article.
Cryptic MYC insertions in Burkitt lymphoma: New data and a review of the literature.
Woroniecka R, Rymkiewicz G, Szafron LM, Blachnio K, Szafron LA, Bystydzienski Z, Pienkowska-Grela B, Borkowska K, Rygier J, Kotyl A, Malawska N, Wojtkowska K, Parada J, Borysiuk A, Murcia Pienkowski V, Rydzanicz M, Grygalewicz B. Woroniecka R, et al. Among authors: rydzanicz m. PLoS One. 2022 Feb 15;17(2):e0263980. doi: 10.1371/journal.pone.0263980. eCollection 2022. PLoS One. 2022. PMID: 35167621 Free PMC article. Review.
Enteroviral central nervous system infections in patients with Lyme neuroborreliosis.
Perlejewski K, Radkowski M, Pawełczyk A, Rydzanicz M, Dzieciątkowski T, Makowiecki M, Paciorek M, Welc-Falęciak R, Horban A, Laskus T. Perlejewski K, et al. Among authors: rydzanicz m. Ticks Tick Borne Dis. 2023 Nov;14(6):102253. doi: 10.1016/j.ttbdis.2023.102253. Epub 2023 Sep 18. Ticks Tick Borne Dis. 2023. PMID: 37729847 Free article.
FINCA syndrome-Defining neurobehavioral phenotype in survivors into late childhood.
Badura-Stronka M, Śmigiel R, Rutkowska K, Szymańska K, Hirschfeld AS, Monkiewicz M, Kosińska J, Wolańska E, Rydzanicz M, Latos-Bieleńska A, Płoski R. Badura-Stronka M, et al. Among authors: rydzanicz m. Mol Genet Genomic Med. 2022 Apr;10(4):e1899. doi: 10.1002/mgg3.1899. Epub 2022 Mar 7. Mol Genet Genomic Med. 2022. PMID: 35255187 Free PMC article.
186 results