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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
[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.
Analysis of the APOE alleles impact in Down's syndrome.
Lambert JC, Pérez-Tur J, Dupire MJ, Delacourte A, Frigard B, Chartier-Harlin MC. Lambert JC, et al. Neurosci Lett. 1996 Dec 6;220(1):57-60. doi: 10.1016/s0304-3940(96)13244-4. Neurosci Lett. 1996. PMID: 8977148
No pathogenic mutations in the persyn gene in Parkinson's disease.
Lincoln S, Gwinn-Hardy K, Goudreau J, Chartier-Harlin MC, Baker M, Mouroux V, Richard F, Destée A, Becquet E, Amouyel P, Lynch T, Hardy J, Farrer M. Lincoln S, et al. Neurosci Lett. 1999 Jan 4;259(1):65-6. doi: 10.1016/s0304-3940(98)00901-x. Neurosci Lett. 1999. PMID: 10027558
127 results