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Cancer and neurodegeneration: Time to move beyond Janus?
Tallaksen CM, Müller U. Tallaksen CM, et al. Among authors: muller u. Neurology. 2017 Mar 21;88(12):1106-1107. doi: 10.1212/WNL.0000000000003727. Epub 2017 Feb 15. Neurology. 2017. PMID: 28202693 No abstract available.
The monogenic primary dystonias.
Müller U. Müller U. Brain. 2009 Aug;132(Pt 8):2005-25. doi: 10.1093/brain/awp172. Epub 2009 Jul 3. Brain. 2009. PMID: 19578124 Review.
KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromes.
Neubauer BA, Waldegger S, Heinzinger J, Hahn A, Kurlemann G, Fiedler B, Eberhard F, Muhle H, Stephani U, Garkisch S, Eeg-Olofsson O, Müller U, Sander T. Neubauer BA, et al. Among authors: muller u. Neurology. 2008 Jul 15;71(3):177-83. doi: 10.1212/01.wnl.0000317090.92185.ec. Neurology. 2008. PMID: 18625963
Rational therapeutic approaches to progressive supranuclear palsy.
Stamelou M, de Silva R, Arias-Carrión O, Boura E, Höllerhage M, Oertel WH, Müller U, Höglinger GU. Stamelou M, et al. Among authors: muller u. Brain. 2010 Jun;133(Pt 6):1578-90. doi: 10.1093/brain/awq115. Epub 2010 May 14. Brain. 2010. PMID: 20472654 Review.
Epigenome-wide DNA methylation profiling in Progressive Supranuclear Palsy reveals major changes at DLX1.
Weber A, Schwarz SC, Tost J, Trümbach D, Winter P, Busato F, Tacik P, Windhorst AC, Fagny M, Arzberger T, McLean C, van Swieten JC, Schwarz J, Vogt Weisenhorn D, Wurst W, Adhikary T, Dickson DW, Höglinger GU, Müller U. Weber A, et al. Among authors: muller u. Nat Commun. 2018 Jul 26;9(1):2929. doi: 10.1038/s41467-018-05325-y. Nat Commun. 2018. PMID: 30050033 Free PMC article.
2,078 results