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

Year Number of Results
1995 1
1996 1
1999 1
2000 1
2001 2
2002 1
2005 1
2006 1
2007 1
2009 2
2010 1
2011 3
2012 1
2013 1
2014 2
2015 1
2017 1
2018 2
2019 1
2020 2
2024 0

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Page 1
[Peroxisomal disorders].
Stradomska TJ. Stradomska TJ. Postepy Biochem. 2018 Dec 29;64(4):359-367. doi: 10.18388/pb.2018_150. Postepy Biochem. 2018. PMID: 30656921 Free article. Review. Polish.
Clinical and molecular characteristics of two transaldolase-deficient patients.
Tylki-Szymanska A, Wamelink MM, Stradomska TJ, Salomons GS, Taybert J, Dąbrowska-Leonik N, Rurarz M. Tylki-Szymanska A, et al. Among authors: stradomska tj. Eur J Pediatr. 2014 Dec;173(12):1679-82. doi: 10.1007/s00431-014-2261-2. Epub 2014 Feb 5. Eur J Pediatr. 2014. PMID: 24497183 Free PMC article.
Mild Zellweger syndrome due to functionally confirmed novel PEX1 variants.
Lipiński P, Stawiński P, Rydzanicz M, Wypchło M, Płoski R, Stradomska TJ, Jurkiewicz E, Ferdinandusse S, Wanders RJA, Vaz FM, Tylki-Szymańska A. Lipiński P, et al. Among authors: stradomska tj. J Appl Genet. 2020 Feb;61(1):87-91. doi: 10.1007/s13353-019-00523-w. Epub 2019 Oct 18. J Appl Genet. 2020. PMID: 31628608 Free PMC article.
Very long-chain fatty acids in Rett syndrome.
Stradomska TJ, Tylki-Szymańska A, Bentkowski Z. Stradomska TJ, et al. Eur J Pediatr. 1999 Mar;158(3):226-9. doi: 10.1007/s004310051055. Eur J Pediatr. 1999. PMID: 10094444
Dominant ELOVL1 mutation causes neurological disorder with ichthyotic keratoderma, spasticity, hypomyelination and dysmorphic features.
Kutkowska-Kaźmierczak A, Rydzanicz M, Chlebowski A, Kłosowska-Kosicka K, Mika A, Gruchota J, Jurkiewicz E, Kowalewski C, Pollak A, Stradomska TJ, Kmieć T, Jakubowski R, Gasperowicz P, Walczak A, Śladowski D, Jankowska-Steifer E, Korniszewski L, Kosińska J, Obersztyn E, Nowak W, Śledziński T, Dziembowski A, Płoski R. Kutkowska-Kaźmierczak A, et al. Among authors: stradomska tj. J Med Genet. 2018 Jun;55(6):408-414. doi: 10.1136/jmedgenet-2017-105172. Epub 2018 Mar 1. J Med Genet. 2018. PMID: 29496980
25 results