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Channelopathy-related SCN10A gene variants predict cerebellar dysfunction in multiple sclerosis.
Roostaei T, Sadaghiani S, Park MT, Mashhadi R, Nazeri A, Noshad S, Salehi MJ, Naghibzadeh M, Moghadasi AN, Owji M, Doosti R, Taheri AP, Rad AS, Azimi A, Chakravarty MM, Voineskos AN, Nazeri A, Sahraian MA. Roostaei T, et al. Among authors: sadaghiani s. Neurology. 2016 Feb 2;86(5):410-7. doi: 10.1212/WNL.0000000000002326. Epub 2016 Jan 6. Neurology. 2016. PMID: 26740675 Free PMC article.
Convergent effects of a functional C3 variant on brain atrophy, demyelination, and cognitive impairment in multiple sclerosis.
Roostaei T, Sadaghiani S, Mashhadi R, Falahatian M, Mohamadi E, Javadian N, Nazeri A, Doosti R, Naser Moghadasi A, Owji M, Hashemi Taheri AP, Shakouri Rad A, Azimi A, Voineskos AN, Nazeri A, Sahraian MA. Roostaei T, et al. Among authors: sadaghiani s. Mult Scler. 2019 Apr;25(4):532-540. doi: 10.1177/1352458518760715. Epub 2018 Feb 27. Mult Scler. 2019. PMID: 29485352
A further TWEAK to multiple sclerosis pathophysiology.
Nazeri A, Heydarpour P, Sadaghiani S, Sahraian MA, Burkly LC, Bar-Or A. Nazeri A, et al. Among authors: sadaghiani s. Mol Neurobiol. 2014 Feb;49(1):78-87. doi: 10.1007/s12035-013-8490-y. Epub 2013 Jul 20. Mol Neurobiol. 2014. PMID: 23873135 Review.
Rapid dynamics of electrophysiological connectome states are heritable.
Jun S, Alderson TH, Malone SM, Harper J, Hunt RH, Thomas KM, Iacono WG, Wilson S, Sadaghiani S. Jun S, et al. Among authors: sadaghiani s. Netw Neurosci. 2024 Dec 10;8(4):1065-1088. doi: 10.1162/netn_a_00391. eCollection 2024. Netw Neurosci. 2024. PMID: 39735507 Free PMC article.
57 results