Villard L - Search Results

1

Rett syndrome from bench to bedside: recent advances.

Ehinger Y, Matagne V, Villard L, Roux JC. Ehinger Y, et al. Among authors: villard l. F1000Res. 2018 Mar 26;7:398. doi: 10.12688/f1000research.14056.1. eCollection 2018. F1000Res. 2018. PMID: 29636907 Free PMC article. Review.

2

Mecp2 deficiency disrupts norepinephrine and respiratory systems in mice.

Viemari JC, Roux JC, Tryba AK, Saywell V, Burnet H, Peña F, Zanella S, Bévengut M, Barthelemy-Requin M, Herzing LB, Moncla A, Mancini J, Ramirez JM, Villard L, Hilaire G. Viemari JC, et al. Among authors: villard l. J Neurosci. 2005 Dec 14;25(50):11521-30. doi: 10.1523/JNEUROSCI.4373-05.2005. J Neurosci. 2005. PMID: 16354910 Free PMC article.

3

[Noradrenaline deficiency as the origin of respiratory disorders in Rett syndrome an animal model].

Villard L, Roux JC. Villard L, et al. Med Sci (Paris). 2006 Jan;22(1):81-3. doi: 10.1051/medsci/200622181. Med Sci (Paris). 2006. PMID: 16386227 Free article. French. No abstract available.

4

Treatment with desipramine improves breathing and survival in a mouse model for Rett syndrome.

Roux JC, Dura E, Moncla A, Mancini J, Villard L. Roux JC, et al. Among authors: villard l. Eur J Neurosci. 2007 Apr;25(7):1915-22. doi: 10.1111/j.1460-9568.2007.05466.x. Eur J Neurosci. 2007. PMID: 17439480

5

[Pharmacological treatment of Rett syndrome improves breathing and survival in a mouse model].

Roux JC, Villard L. Roux JC, et al. Among authors: villard l. Med Sci (Paris). 2007 Oct;23(10):805-7. doi: 10.1051/medsci/20072310805. Med Sci (Paris). 2007. PMID: 17937887 Free article. French. No abstract available.

6

Expression of methyl CpG binding protein 2 (Mecp2) during the postnatal development of the mouse brainstem.

Dura E, Villard L, Roux JC. Dura E, et al. Among authors: villard l. Brain Res. 2008 Oct 21;1236:176-84. doi: 10.1016/j.brainres.2008.08.021. Epub 2008 Aug 16. Brain Res. 2008. PMID: 18761004

7

Tyrosine hydroxylase deficit in the chemoafferent and the sympathoadrenergic pathways of the Mecp2 deficient mouse.

Roux JC, Dura E, Villard L. Roux JC, et al. Among authors: villard l. Neurosci Lett. 2008 Dec 5;447(1):82-6. doi: 10.1016/j.neulet.2008.09.045. Epub 2008 Sep 24. Neurosci Lett. 2008. PMID: 18834926

8

Spatiotemporal expression in mouse brain of Kiaa2022, a gene disrupted in two patients with severe mental retardation.

Cantagrel V, Haddad MR, Ciofi P, Andrieu D, Lossi AM, Maldergem Lv, Roux JC, Villard L. Cantagrel V, et al. Among authors: villard l. Gene Expr Patterns. 2009 Sep;9(6):423-9. doi: 10.1016/j.gep.2009.06.001. Epub 2009 Jun 11. Gene Expr Patterns. 2009. PMID: 19524067

9

Biogenic amines in Rett syndrome: the usual suspects.

Roux JC, Villard L. Roux JC, et al. Among authors: villard l. Behav Genet. 2010 Jan;40(1):59-75. doi: 10.1007/s10519-009-9303-y. Epub 2009 Oct 23. Behav Genet. 2010. PMID: 19851857 Review.

10

Progressive noradrenergic deficits in the locus coeruleus of Mecp2 deficient mice.

Roux JC, Panayotis N, Dura E, Villard L. Roux JC, et al. Among authors: villard l. J Neurosci Res. 2010 May 15;88(7):1500-9. doi: 10.1002/jnr.22312. J Neurosci Res. 2010. PMID: 19998492

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