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Tominersen in Adults with Manifest Huntington's Disease.
McColgan P, Thobhani A, Boak L, Schobel SA, Nicotra A, Palermo G, Trundell D, Zhou J, Schlegel V, Sanwald Ducray P, Hawellek DJ, Dorn J, Simillion C, Lindemann M, Wheelock V, Durr A, Anderson KE, Long JD, Wild EJ, Landwehrmeyer GB, Leavitt BR, Tabrizi SJ, Doody R; GENERATION HD1 Investigators. McColgan P, et al. N Engl J Med. 2023 Dec 7;389(23):2203-2205. doi: 10.1056/NEJMc2300400. N Engl J Med. 2023. PMID: 38055260 No abstract available.
Worldwide barriers to genetic testing for movement disorders.
Gatto EM, Walker RH, Gonzalez C, Cesarini M, Cossu G, Stephen CD, Balint B, Rodríguez-Violante M, Jankovic J, Morgante F, Jinnah HA; Rare Movement Disorders Study Group of the International Parkinson Disease, Movement Disorders Society. Gatto EM, et al. Eur J Neurol. 2021 Jun;28(6):1901-1909. doi: 10.1111/ene.14826. Epub 2021 Apr 9. Eur J Neurol. 2021. PMID: 33730413
A novel mutation in PSEN1 (p.Arg41Ser) in an Argentinian woman with early onset Parkinsonism.
Gatto EM, Rojas GJ, Nemirovsky SI, Da Prat G, Persi G, Cesarini M, Etcheverry JL, Rojas NG, Parisi V, Cordoba M, Sevlever G, Allegri RF, Turjanski AG. Gatto EM, et al. Among authors: etcheverry jl. Parkinsonism Relat Disord. 2020 Aug;77:21-25. doi: 10.1016/j.parkreldis.2020.06.005. Epub 2020 Jun 17. Parkinsonism Relat Disord. 2020. PMID: 32590294
Huntington disease: Advances in the understanding of its mechanisms.
Gatto EM, Rojas NG, Persi G, Etcheverry JL, Cesarini ME, Perandones C. Gatto EM, et al. Among authors: etcheverry jl. Clin Park Relat Disord. 2020 May 6;3:100056. doi: 10.1016/j.prdoa.2020.100056. eCollection 2020. Clin Park Relat Disord. 2020. PMID: 34316639 Free PMC article. Review.
43 results