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Analysis of ICAM1 gene polymorphism in Slovak multiple sclerosis patients.
Shawkatová I, Javor J, Párnická Z, Bucová M, Čopíková-Cudráková D, Michalík J, Gmitterová K, Čierny D, Buc M, Ďurmanová V. Shawkatová I, et al. Among authors: copikova cudrakova d. Folia Microbiol (Praha). 2017 Jul;62(4):287-293. doi: 10.1007/s12223-017-0499-6. Epub 2017 Jan 27. Folia Microbiol (Praha). 2017. PMID: 28130760
The +190 G/A (rs1799864) polymorphism in the C-C chemokine receptor 2 (CCR2) gene is associated with susceptibility to multiple sclerosis in HLA-DRB1*15:01-negative individuals.
Javor J, Párnická Z, Michalik J, Čopíková-Cudráková D, Shawkatová I, Ďurmanová V, Gmitterová K, Klímová E, Bucová M, Buc M. Javor J, et al. Among authors: copikova cudrakova d. J Neurol Sci. 2015 Feb 15;349(1-2):138-42. doi: 10.1016/j.jns.2015.01.002. Epub 2015 Jan 9. J Neurol Sci. 2015. PMID: 25604634
Adrenoleukodystrophy--a new mutation identified.
Vachalova I, Chandoga J, Petrovic R, Copikova-Cudrakova D, Sykora M, Traubner P. Vachalova I, et al. Among authors: copikova cudrakova d. Bratisl Lek Listy. 2007;108(10-11):462-6. Bratisl Lek Listy. 2007. PMID: 18306728
Natalizumab treatment shows low cumulative probabilities of confirmed disability worsening to EDSS milestones in the long-term setting.
Trojano M, Butzkueven H, Kappos L, Wiendl H, Spelman T, Pellegrini F, Chen Y, Dong Q, Koendgen H, Belachew S; Tysabri® Observational Program (TOP) Investigators. Trojano M, et al. Mult Scler Relat Disord. 2018 Aug;24:11-19. doi: 10.1016/j.msard.2018.04.020. Epub 2018 May 2. Mult Scler Relat Disord. 2018. PMID: 29860197 Free article.