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Generation of an induced pluripotent stem cell line (CIMAi001-A) from a compound heterozygous Primary Hyperoxaluria Type I (PH1) patient carrying p.G170R and p.R122* mutations in the AGXT gene.
Martinez-Turrillas R, Rodriguez-Diaz S, Rodriguez-Marquez P, Martin-Mallo A, Salido E, Beck BB, Prosper F, Rodriguez-Madoz JR. Martinez-Turrillas R, et al. Among authors: salido e. Stem Cell Res. 2019 Dec;41:101626. doi: 10.1016/j.scr.2019.101626. Epub 2019 Oct 18. Stem Cell Res. 2019. PMID: 31715429 Free article.
[Molecular pathology of primary hyperoxaluria].
Santana A, Torres A, Salido E. Santana A, et al. Among authors: salido e. Nefrologia. 2003;23 Suppl 1:90-7. Nefrologia. 2003. PMID: 12708368 Free article. Review. Spanish. No abstract available.
Primary hyperoxaluria in a compound heterozygote infant.
Mayordomo-Colunga J, Riverol D, Salido E, Santos F. Mayordomo-Colunga J, et al. Among authors: salido e. World J Pediatr. 2011 May;7(2):173-5. doi: 10.1007/s12519-010-0214-z. Epub 2010 Jun 12. World J Pediatr. 2011. PMID: 20549407
Primary hyperoxalurias: disorders of glyoxylate detoxification.
Salido E, Pey AL, Rodriguez R, Lorenzo V. Salido E, et al. Biochim Biophys Acta. 2012 Sep;1822(9):1453-64. doi: 10.1016/j.bbadis.2012.03.004. Epub 2012 Mar 14. Biochim Biophys Acta. 2012. PMID: 22446032 Free article. Review.
Novel findings in patients with primary hyperoxaluria type III and implications for advanced molecular testing strategies.
Beck BB, Baasner A, Buescher A, Habbig S, Reintjes N, Kemper MJ, Sikora P, Mache C, Pohl M, Stahl M, Toenshoff B, Pape L, Fehrenbach H, Jacob DE, Grohe B, Wolf MT, Nürnberg G, Yigit G, Salido EC, Hoppe B. Beck BB, et al. Among authors: salido ec. Eur J Hum Genet. 2013 Feb;21(2):162-72. doi: 10.1038/ejhg.2012.139. Epub 2012 Jul 11. Eur J Hum Genet. 2013. PMID: 22781098 Free PMC article.
269 results