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421 results

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Page 1
Dysfunctional Networks in Functional Dystonia.
Ricciardi L, Bologna M, Marsili L, Espay AJ. Ricciardi L, et al. Among authors: espay aj. Adv Neurobiol. 2023;31:157-176. doi: 10.1007/978-3-031-26220-3_9. Adv Neurobiol. 2023. PMID: 37338701 Review.
Resolving 'vascular parkinsonism' -COL22A1 as a genetic adult-onset leukoencephalopathy.
Marsili L, Kauffman MA, Rufin Florat D, Zaidi A, Botsford V, Sharma J, Keeling EG, Broderick JP, Sumanas S, Espay AJ. Marsili L, et al. Among authors: espay aj. Parkinsonism Relat Disord. 2023 Oct 23;117:105898. doi: 10.1016/j.parkreldis.2023.105898. Online ahead of print. Parkinsonism Relat Disord. 2023. PMID: 39492172
Functional ataxia in a specialized ataxia center.
Corazza LA, Reis Rosa AB, Tonholo Silva TY, Rezende Filho FM, Maranhão-Filho PA, Pedroso JL, Barsottini OGP, Espay AJ. Corazza LA, et al. Among authors: espay aj. Parkinsonism Relat Disord. 2024 Mar;120:106006. doi: 10.1016/j.parkreldis.2024.106006. Epub 2024 Jan 14. Parkinsonism Relat Disord. 2024. PMID: 38244461
Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study.
Rizig M, Bandres-Ciga S, Makarious MB, Ojo OO, Crea PW, Abiodun OV, Levine KS, Abubakar SA, Achoru CO, Vitale D, Adeniji OA, Agabi OP, Koretsky MJ, Agulanna U, Hall DA, Akinyemi RO, Xie T, Ali MW, Shamim EA, Ani-Osheku I, Padmanaban M, Arigbodi OM, Standaert DG, Bello AH, Dean MN, Erameh CO, Elsayed I, Farombi TH, Okunoye O, Fawale MB, Billingsley KJ, Imarhiagbe FA, Jerez PA, Iwuozo EU, Baker B, Komolafe MA, Malik L, Nwani PO, Daida K, Nwazor EO, Miano-Burkhardt A, Nyandaiti YW, Fang ZH, Obiabo YO, Kluss JH, Odeniyi OA, Hernandez DG, Odiase FE, Tayebi N, Ojini FI, Sidranksy E, Onwuegbuzie GA, D'Souza AM, Osaigbovo GO, Berhe B, Osemwegie N, Reed X, Oshinaike OO, Leonard HL, Otubogun FM, Alvarado CX, Oyakhire SI, Ozomma SI, Samuel SC, Taiwo FT, Wahab KW, Zubair YA, Iwaki H, Kim JJ, Morris HR, Hardy J, Nalls MA, Heilbron K, Norcliffe-Kaufmann L; Nigeria Parkinson Disease Research Network; International Parkinson's Disease Genomics Consortium Africa; Black and African American Connections to Parkinson's Disease Study Group; 23andMe Research Team; Blauwendraat C, Houlden H, Singleton A, Okubadejo NU; Global Parkinson's Genetics Program. Rizig M, et al. Lancet Neurol. 2023 Nov;22(11):1015-1025. doi: 10.1016/S1474-4422(23)00283-1. Epub 2023 Aug 23. Lancet Neurol. 2023. PMID: 37633302 Free PMC article.
Defining the causes of sporadic Parkinson's disease in the global Parkinson's genetics program (GP2).
Towns C, Richer M, Jasaityte S, Stafford EJ, Joubert J, Antar T, Martinez-Carrasco A, Makarious MB, Casey B, Vitale D, Levine K, Leonard H, Pantazis CB, Screven LA, Hernandez DG, Wegel CE, Solle J, Nalls MA, Blauwendraat C, Singleton AB, Tan MMX, Iwaki H, Morris HR; Global Parkinson’s Genetics Program (GP2). Towns C, et al. NPJ Parkinsons Dis. 2023 Sep 12;9(1):131. doi: 10.1038/s41531-023-00533-w. NPJ Parkinsons Dis. 2023. PMID: 37699923 Free PMC article.
421 results