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Page 1
Targeting chelatable iron as a therapeutic modality in Parkinson's disease.
Devos D, Moreau C, Devedjian JC, Kluza J, Petrault M, Laloux C, Jonneaux A, Ryckewaert G, Garçon G, Rouaix N, Duhamel A, Jissendi P, Dujardin K, Auger F, Ravasi L, Hopes L, Grolez G, Firdaus W, Sablonnière B, Strubi-Vuillaume I, Zahr N, Destée A, Corvol JC, Pöltl D, Leist M, Rose C, Defebvre L, Marchetti P, Cabantchik ZI, Bordet R. Devos D, et al. Among authors: strubi vuillaume i. Antioxid Redox Signal. 2014 Jul 10;21(2):195-210. doi: 10.1089/ars.2013.5593. Epub 2014 Feb 6. Antioxid Redox Signal. 2014. PMID: 24251381 Free PMC article. Clinical Trial.
TMEM240 mutations cause spinocerebellar ataxia 21 with mental retardation and severe cognitive impairment.
Delplanque J, Devos D, Huin V, Genet A, Sand O, Moreau C, Goizet C, Charles P, Anheim M, Monin ML, Buée L, Destée A, Grolez G, Delmaire C, Dujardin K, Dellacherie D, Brice A, Stevanin G, Strubi-Vuillaume I, Dürr A, Sablonnière B. Delplanque J, et al. Among authors: strubi vuillaume i. Brain. 2014 Oct;137(Pt 10):2657-63. doi: 10.1093/brain/awu202. Epub 2014 Jul 28. Brain. 2014. PMID: 25070513
Expanding the phenotype of SCA19/22: Parkinsonism, cognitive impairment and epilepsy.
Huin V, Strubi-Vuillaume I, Dujardin K, Brion M, Delliaux M, Dellacherie D, Cuvellier JC, Cuisset JM, Riquet A, Moreau C, Defebvre L, Sablonnière B, Devos D. Huin V, et al. Among authors: strubi vuillaume i. Parkinsonism Relat Disord. 2017 Dec;45:85-89. doi: 10.1016/j.parkreldis.2017.09.014. Epub 2017 Sep 19. Parkinsonism Relat Disord. 2017. PMID: 28947073 Free article.
Writing tremor: Should we look for a TOR1A mutation?
Aerts C, Cassim F, Strubi-Vuillaume I, Destée A, Sablonnière B, Collod-Béroud G, Defebvre L, Kreisler A. Aerts C, et al. Among authors: strubi vuillaume i. J Neurol Sci. 2017 Nov 15;382:146-147. doi: 10.1016/j.jns.2017.09.048. Epub 2017 Oct 2. J Neurol Sci. 2017. PMID: 29111010 Free article. No abstract available.
Amyotrophic lateral sclerosis associated with a pathological expansion in the ATXN7 gene.
Cluse F, Bernard E, Strubi-Vuillaume I, Devos D, Mouzat K, Lumbroso S, Froment Tilikete C, Thobois S, Pegat A. Cluse F, et al. Among authors: strubi vuillaume i. Amyotroph Lateral Scler Frontotemporal Degener. 2022 Aug;23(5-6):470-472. doi: 10.1080/21678421.2021.1998537. Epub 2021 Dec 6. Amyotroph Lateral Scler Frontotemporal Degener. 2022. PMID: 34870541