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Page 1
CSF α-synuclein seed amplification kinetic profiles are associated with cognitive decline in Parkinson's disease.
Brockmann K, Lerche S, Baiardi S, Rossi M, Wurster I, Quadalti C, Roeben B, Mammana A, Zimmermann M, Hauser AK, Deuschle C, Schulte C, Liepelt-Scarfone I, Gasser T, Parchi P. Brockmann K, et al. Among authors: hauser ak. NPJ Parkinsons Dis. 2024 Jan 20;10(1):24. doi: 10.1038/s41531-023-00627-5. NPJ Parkinsons Dis. 2024. PMID: 38242875 Free PMC article.
Author Correction: Accurate long-read sequencing identified GBA1 as major risk factor in the Luxembourgish Parkinson's study.
Pachchek S, Landoulsi Z, Pavelka L, Schulte C, Buena-Atienza E, Gross C, Hauser AK, Reddy Bobbili D, Casadei N, May P, Krüger R; NCER-PD Consortium. Pachchek S, et al. Among authors: hauser ak. NPJ Parkinsons Dis. 2023 Dec 18;9(1):168. doi: 10.1038/s41531-023-00613-x. NPJ Parkinsons Dis. 2023. PMID: 38110362 Free PMC article. No abstract available.
Impact of APOE Genotype on Cognition in Idiopathic and Genetic Forms of Parkinson's Disease.
Koros C, Brockmann K, Simitsi AM, Bougea A, Liu H, Hauser AK, Schulte C, Lerche S, Pachi I, Papagiannakis N, Antonelou R, Zahou A, Wurster I, Efthymiopoulou E, Beratis I, Maniati M, Moraitou M, Michelakakis H, Paraskevas G, Papageorgiou SG, Potagas C, Papadimitriou D, Bozi M, Stamelou M, Gasser T, Stefanis L. Koros C, et al. Among authors: hauser ak. Mov Disord. 2023 May;38(5):907-909. doi: 10.1002/mds.29399. Epub 2023 May 6. Mov Disord. 2023. PMID: 37148559 No abstract available.
Association between CSF alpha-synuclein seeding activity and genetic status in Parkinson's disease and dementia with Lewy bodies.
Brockmann K, Quadalti C, Lerche S, Rossi M, Wurster I, Baiardi S, Roeben B, Mammana A, Zimmermann M, Hauser AK, Deuschle C, Schulte C, Waniek K, Lachmann I, Sjödin S, Brinkmalm A, Blennow K, Zetterberg H, Gasser T, Parchi P. Brockmann K, et al. Among authors: hauser ak. Acta Neuropathol Commun. 2021 Oct 30;9(1):175. doi: 10.1186/s40478-021-01276-6. Acta Neuropathol Commun. 2021. PMID: 34717775 Free PMC article.
A Novel SNCA A30G Mutation Causes Familial Parkinson's Disease.
Liu H, Koros C, Strohäker T, Schulte C, Bozi M, Varvaresos S, Ibáñez de Opakua A, Simitsi AM, Bougea A, Voumvourakis K, Maniati M, Papageorgiou SG, Hauser AK, Becker S, Zweckstetter M, Stefanis L, Gasser T. Liu H, et al. Among authors: hauser ak. Mov Disord. 2021 Jul;36(7):1624-1633. doi: 10.1002/mds.28534. Epub 2021 Feb 22. Mov Disord. 2021. PMID: 33617693
51 results