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Centrosomal cohesion deficits as cellular biomarker in lymphoblastoid cell lines from LRRK2 Parkinson's disease patients.
Fernández B, Lara Ordóñez AJ, Fdez E, Mutez E, Comptdaer T, Leghay C, Kreisler A, Simonin C, Vandewynckel L, Defebvre L, Destée A, Bleuse S, Taymans JM, Chartier-Harlin MC, Hilfiker S. Fernández B, et al. Among authors: destee a. Biochem J. 2019 Oct 15;476(19):2797-2813. doi: 10.1042/BCJ20190315. Biochem J. 2019. PMID: 31527116 Free PMC article.
Transcriptional profile of Parkinson blood mononuclear cells with LRRK2 mutation.
Mutez E, Larvor L, Leprêtre F, Mouroux V, Hamalek D, Kerckaert JP, Pérez-Tur J, Waucquier N, Vanbesien-Mailliot C, Duflot A, Devos D, Defebvre L, Kreisler A, Frigard B, Destée A, Chartier-Harlin MC. Mutez E, et al. Among authors: destee a. Neurobiol Aging. 2011 Oct;32(10):1839-48. doi: 10.1016/j.neurobiolaging.2009.10.016. Epub 2010 Jan 22. Neurobiol Aging. 2011. PMID: 20096956
Involvement of the immune system, endocytosis and EIF2 signaling in both genetically determined and sporadic forms of Parkinson's disease.
Mutez E, Nkiliza A, Belarbi K, de Broucker A, Vanbesien-Mailliot C, Bleuse S, Duflot A, Comptdaer T, Semaille P, Blervaque R, Hot D, Leprêtre F, Figeac M, Destée A, Chartier-Harlin MC. Mutez E, et al. Among authors: destee a. Neurobiol Dis. 2014 Mar;63:165-70. doi: 10.1016/j.nbd.2013.11.007. Epub 2013 Nov 20. Neurobiol Dis. 2014. PMID: 24269915
NADPH oxidases in Parkinson's disease: a systematic review.
Belarbi K, Cuvelier E, Destée A, Gressier B, Chartier-Harlin MC. Belarbi K, et al. Among authors: destee a. Mol Neurodegener. 2017 Nov 13;12(1):84. doi: 10.1186/s13024-017-0225-5. Mol Neurodegener. 2017. PMID: 29132391 Free PMC article. Review.
Early cognitive decline after bilateral subthalamic deep brain stimulation in Parkinson's disease patients with GBA mutations.
Mangone G, Bekadar S, Cormier-Dequaire F, Tahiri K, Welaratne A, Czernecki V, Pineau F, Karachi C, Castrioto A, Durif F, Tranchant C, Devos D, Thobois S, Meissner WG, Navarro MS, Cornu P, Lesage S, Brice A, Welter ML, Corvol JC; contributors/investigators. Mangone G, et al. Parkinsonism Relat Disord. 2020 Jul;76:56-62. doi: 10.1016/j.parkreldis.2020.04.002. Epub 2020 Jun 9. Parkinsonism Relat Disord. 2020. PMID: 32866938
SNCA locus duplication carriers: from genetics to Parkinson disease phenotypes.
Mutez E, Leprêtre F, Le Rhun E, Larvor L, Duflot A, Mouroux V, Kerckaert JP, Figeac M, Dujardin K, Destée A, Chartier-Harlin MC. Mutez E, et al. Among authors: destee a. Hum Mutat. 2011 Apr;32(4):E2079-90. doi: 10.1002/humu.21459. Epub 2011 Feb 8. Hum Mutat. 2011. PMID: 21412942
Xenopus laevis as a Model to Identify Translation Impairment.
de Broucker A, Semaille P, Cailliau K, Martoriati A, Comptdaer T, Bodart JF, Destée A, Chartier-Harlin MC. de Broucker A, et al. Among authors: destee a. J Vis Exp. 2015 Sep 27;(103):52724. doi: 10.3791/52724. J Vis Exp. 2015. PMID: 26437037 Free PMC article.
Overexpression of Wild-Type Human Alpha-Synuclein Causes Metabolism Abnormalities in Thy1-aSYN Transgenic Mice.
Cuvelier E, Méquinion M, Leghay C, Sibran W, Stievenard A, Sarchione A, Bonte MA, Vanbesien-Mailliot C, Viltart O, Saitoski K, Caron E, Labarthe A, Comptdaer T, Semaille P, Carrié H, Mutez E, Gressier B, Destée A, Chartier-Harlin MC, Belarbi K. Cuvelier E, et al. Among authors: destee a. Front Mol Neurosci. 2018 Oct 2;11:321. doi: 10.3389/fnmol.2018.00321. eCollection 2018. Front Mol Neurosci. 2018. PMID: 30333721 Free PMC article.
466 results