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Page 1
A candidate loss-of-function variant in SGIP1 causes synaptic dysfunction and recessive parkinsonism.
Decet M, Scott P, Kuenen S, Meftah D, Swerts J, Calatayud C, Gallego SF, Kaempf N, Nachman E, Praschberger R, Schoovaerts N, Tang CC, Eidelberg D, Al Adawi S, Al Asmi A, Nandhagopal R, Verstreken P. Decet M, et al. Among authors: praschberger r. Cell Rep Med. 2024 Oct 15;5(10):101749. doi: 10.1016/j.xcrm.2024.101749. Epub 2024 Sep 26. Cell Rep Med. 2024. PMID: 39332416 Free PMC article.
Elevated α-synuclein levels inhibit mitophagic flux.
Kinnart I, Manders L, Heyninck T, Imberechts D, Praschberger R, Schoovaerts N, Verfaillie C, Verstreken P, Vandenberghe W. Kinnart I, et al. Among authors: praschberger r. NPJ Parkinsons Dis. 2024 Apr 9;10(1):80. doi: 10.1038/s41531-024-00696-0. NPJ Parkinsons Dis. 2024. PMID: 38594264 Free PMC article.
Neuronal identity defines α-synuclein and tau toxicity.
Praschberger R, Kuenen S, Schoovaerts N, Kaempf N, Singh J, Janssens J, Swerts J, Nachman E, Calatayud C, Aerts S, Poovathingal S, Verstreken P. Praschberger R, et al. Neuron. 2023 May 17;111(10):1577-1590.e11. doi: 10.1016/j.neuron.2023.02.033. Epub 2023 Mar 21. Neuron. 2023. PMID: 36948206 Free PMC article.
Neurodegeneration cell per cell.
Balusu S, Praschberger R, Lauwers E, De Strooper B, Verstreken P. Balusu S, et al. Among authors: praschberger r. Neuron. 2023 Mar 15;111(6):767-786. doi: 10.1016/j.neuron.2023.01.016. Epub 2023 Feb 13. Neuron. 2023. PMID: 36787752 Free article. Review.
Expanding the Phenotype and Genetic Defects Associated with the GOSR2 Gene.
Praschberger R, Balint B, Mencacci NE, Hersheson J, Rubio-Agusti I, Kullmann DM, Bettencourt C, Bhatia K, Houlden H. Praschberger R, et al. Mov Disord Clin Pract. 2015 Jun 17;2(3):271-273. doi: 10.1002/mdc3.12190. eCollection 2015 Sep. Mov Disord Clin Pract. 2015. PMID: 30363482 Free PMC article.