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Transaldolase deficiency in two new patients with a relative mild phenotype.
Tylki-Szymańska A, Stradomska TJ, Wamelink MM, Salomons GS, Taybert J, Pawłowska J, Jakobs C. Tylki-Szymańska A, et al. Among authors: stradomska tj. Mol Genet Metab. 2009 May;97(1):15-7. doi: 10.1016/j.ymgme.2009.01.016. Epub 2009 Feb 10. Mol Genet Metab. 2009. PMID: 19299175
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.
29 results