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Page 1
A Case of Chorea with Slow Saccades Caused by NKX2-1 Mutation.
Vercammen J, Terryn J, Van Daele S, Vermeer S, Vandenberghe W. Vercammen J, et al. Among authors: terryn j. Mov Disord Clin Pract. 2024 Jun;11(6):738-741. doi: 10.1002/mdc3.14013. Epub 2024 Mar 7. Mov Disord Clin Pract. 2024. PMID: 38454250 No abstract available.
Intracerebroventricular delivery of vascular endothelial growth factor in patients with amyotrophic lateral sclerosis, a phase I study.
Van Damme P, Tilkin P, Mercer KJ, Terryn J, D'Hondt A, Herne N, Tousseyn T, Claeys KG, Thal DR, Zachrisson O, Almqvist P, Nuttin B, Jerling M, Bernadotte F, Haegerstrand A, Robberecht W. Van Damme P, et al. Among authors: terryn j. Brain Commun. 2020 Sep 29;2(2):fcaa160. doi: 10.1093/braincomms/fcaa160. eCollection 2020. Brain Commun. 2020. PMID: 33977260 Free PMC article.
The Characteristic Eye Movement Disorder of RFC1-Linked CANVAS.
Terryn J, Van Eesbeeck A, Vermeer S, Vandenberghe W. Terryn J, et al. Mov Disord Clin Pract. 2020 Jan 24;7(2):230-231. doi: 10.1002/mdc3.12896. eCollection 2020 Feb. Mov Disord Clin Pract. 2020. PMID: 33636721 Free PMC article. No abstract available.
Generation of a human induced pluripotent stem cell-based model for tauopathies combining three microtubule-associated protein TAU mutations which displays several phenotypes linked to neurodegeneration.
García-León JA, Cabrera-Socorro A, Eggermont K, Swijsen A, Terryn J, Fazal R, Nami F, Ordovás L, Quiles A, Lluis F, Serneels L, Wierda K, Sierksma A, Kreir M, Pestana F, Van Damme P, De Strooper B, Thorrez L, Ebneth A, Verfaillie CM. García-León JA, et al. Among authors: terryn j. Alzheimers Dement. 2018 Oct;14(10):1261-1280. doi: 10.1016/j.jalz.2018.05.007. Epub 2018 Jul 20. Alzheimers Dement. 2018. PMID: 30036493 Free article.