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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. Neurobiol Dis. 2014 Mar;63:165-70. doi: 10.1016/j.nbd.2013.11.007. Epub 2013 Nov 20. Neurobiol Dis. 2014. PMID: 24269915
[Huntington disease: disclosing the gene].
Destée A, Chartier-Harlin MC. Destée A, et al. Presse Med. 1995 Feb 11;24(6):312-6. Presse Med. 1995. PMID: 7899393 Review. French.
Genetic analysis of synphilin-1 in familial Parkinson's disease.
Farrer M, Destée A, Levecque C, Singleton A, Engelender S, Becquet E, Mouroux V, Richard F, Defebvre L, Crook R, Hernandez D, Ross CA, Hardy J, Amouyel P, Chartier-Harlin MC. Farrer M, et al. Neurobiol Dis. 2001 Apr;8(2):317-23. doi: 10.1006/nbdi.2000.0326. Neurobiol Dis. 2001. PMID: 11300726
Alpha-synuclein locus duplication as a cause of familial Parkinson's disease.
Chartier-Harlin MC, Kachergus J, Roumier C, Mouroux V, Douay X, Lincoln S, Levecque C, Larvor L, Andrieux J, Hulihan M, Waucquier N, Defebvre L, Amouyel P, Farrer M, Destée A. Chartier-Harlin MC, et al. Lancet. 2004 Sep 25-Oct 1;364(9440):1167-9. doi: 10.1016/S0140-6736(04)17103-1. Lancet. 2004. PMID: 15451224
[Parkinson disease: genetics and neuronal death].
Destée A, Mutez E, Kreisler A, Vanbesien-Maillot C, Chartier-Harlin MC. Destée A, et al. Rev Neurol (Paris). 2009 Apr;165 Spec No 2:F80-5. Rev Neurol (Paris). 2009. PMID: 19593875 Review. French. No abstract available.
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. 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
Independent and joint effects of the MAPT and SNCA genes in Parkinson disease.
Elbaz A, Ross OA, Ioannidis JP, Soto-Ortolaza AI, Moisan F, Aasly J, Annesi G, Bozi M, Brighina L, Chartier-Harlin MC, Destée A, Ferrarese C, Ferraris A, Gibson JM, Gispert S, Hadjigeorgiou GM, Jasinska-Myga B, Klein C, Krüger R, Lambert JC, Lohmann K, van de Loo S, Loriot MA, Lynch T, Mellick GD, Mutez E, Nilsson C, Opala G, Puschmann A, Quattrone A, Sharma M, Silburn PA, Stefanis L, Uitti RJ, Valente EM, Vilariño-Güell C, Wirdefeldt K, Wszolek ZK, Xiromerisiou G, Maraganore DM, Farrer MJ; Genetic Epidemiology of Parkinson's Disease (GEO-PD) Consortium. Elbaz A, et al. Ann Neurol. 2011 May;69(5):778-92. doi: 10.1002/ana.22321. Epub 2011 Mar 9. Ann Neurol. 2011. PMID: 21391235 Free PMC article.
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