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Nomenclature of Genetic Movement Disorders: Recommendations of the International Parkinson and Movement Disorder Society Task Force - An Update.
Lange LM, Gonzalez-Latapi P, Rajalingam R, Tijssen MAJ, Ebrahimi-Fakhari D, Gabbert C, Ganos C, Ghosh R, Kumar KR, Lang AE, Rossi M, van der Veen S, van de Warrenburg B, Warner T, Lohmann K, Klein C, Marras C; on behalf of the Task Force on Genetic Nomenclature in Movement Disorders. Lange LM, et al. Among authors: warner t. Mov Disord. 2022 May;37(5):905-935. doi: 10.1002/mds.28982. Epub 2022 Apr 28. Mov Disord. 2022. PMID: 35481685 Review.
Emerging common molecular pathways for primary dystonia.
Ledoux MS, Dauer WT, Warner TT. Ledoux MS, et al. Among authors: warner tt. Mov Disord. 2013 Jun 15;28(7):968-81. doi: 10.1002/mds.25547. Mov Disord. 2013. PMID: 23893453 Free PMC article. Review.
MSA-C or SCA 17? A clinicopathological case update.
Doherty KM, De Pablo-Fernandez E, Houlden H, Polke JM, Lees AJ, Warner TT, Holton JL. Doherty KM, et al. Among authors: warner tt. Mov Disord. 2016 Oct;31(10):1582-1584. doi: 10.1002/mds.26741. Mov Disord. 2016. PMID: 27477540 No abstract available.
1,069 results