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67 results

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Page 1
Analysis of monocyte infiltration in MPTP mice reveals that microglial CX3CR1 protects against neurotoxic over-induction of monocyte-attracting CCL2 by astrocytes.
Parillaud VR, Lornet G, Monnet Y, Privat AL, Haddad AT, Brochard V, Bekaert A, de Chanville CB, Hirsch EC, Combadière C, Hunot S, Lobsiger CS. Parillaud VR, et al. Among authors: brochard v. J Neuroinflammation. 2017 Mar 21;14(1):60. doi: 10.1186/s12974-017-0830-9. J Neuroinflammation. 2017. PMID: 28320442 Free PMC article.
Longitudinal analysis of impulse control disorders in Parkinson disease.
Corvol JC, Artaud F, Cormier-Dequaire F, Rascol O, Durif F, Derkinderen P, Marques AR, Bourdain F, Brandel JP, Pico F, Lacomblez L, Bonnet C, Brefel-Courbon C, Ory-Magne F, Grabli D, Klebe S, Mangone G, You H, Mesnage V, Lee PC, Brice A, Vidailhet M, Elbaz A; DIGPD Study Group. Corvol JC, et al. Neurology. 2018 Jul 17;91(3):e189-e201. doi: 10.1212/WNL.0000000000005816. Epub 2018 Jun 20. Neurology. 2018. PMID: 29925549 Free PMC article.
Non cell-autonomous role of DCC in the guidance of the corticospinal tract at the midline.
Welniarz Q, Morel MP, Pourchet O, Gallea C, Lamy JC, Cincotta M, Doulazmi M, Belle M, Méneret A, Trouillard O, Ruiz M, Brochard V, Meunier S, Trembleau A, Vidailhet M, Chédotal A, Dusart I, Roze E. Welniarz Q, et al. Among authors: brochard v. Sci Rep. 2017 Mar 24;7(1):410. doi: 10.1038/s41598-017-00514-z. Sci Rep. 2017. PMID: 28341853 Free PMC article.
Congenital mirror movements caused by a mutation in the DCC gene.
Meneret A, Trouillard O, Brochard V, Roze E. Meneret A, et al. Among authors: brochard v. Dev Med Child Neurol. 2015 Aug;57(8):776. doi: 10.1111/dmcn.12810. Epub 2015 May 22. Dev Med Child Neurol. 2015. PMID: 26011025 Free article. No abstract available.
A novel DCC mutation and genetic heterogeneity in congenital mirror movements.
Depienne C, Cincotta M, Billot S, Bouteiller D, Groppa S, Brochard V, Flamand C, Hubsch C, Meunier S, Giovannelli F, Klebe S, Corvol JC, Vidailhet M, Brice A, Roze E. Depienne C, et al. Among authors: brochard v. Neurology. 2011 Jan 18;76(3):260-4. doi: 10.1212/WNL.0b013e318207b1e0. Neurology. 2011. PMID: 21242494
Impaired saccadic adaptation in DYT11 dystonia.
Hubsch C, Vidailhet M, Rivaud-Péchoux S, Pouget P, Brochard V, Degos B, Pélisson D, Golmard JL, Gaymard B, Roze E. Hubsch C, et al. Among authors: brochard v. J Neurol Neurosurg Psychiatry. 2011 Oct;82(10):1103-6. doi: 10.1136/jnnp.2010.232793. Epub 2011 Mar 8. J Neurol Neurosurg Psychiatry. 2011. PMID: 21386109
RAD51 haploinsufficiency causes congenital mirror movements in humans.
Depienne C, Bouteiller D, Méneret A, Billot S, Groppa S, Klebe S, Charbonnier-Beaupel F, Corvol JC, Saraiva JP, Brueggemann N, Bhatia K, Cincotta M, Brochard V, Flamand-Roze C, Carpentier W, Meunier S, Marie Y, Gaussen M, Stevanin G, Wehrle R, Vidailhet M, Klein C, Dusart I, Brice A, Roze E. Depienne C, et al. Among authors: brochard v. Am J Hum Genet. 2012 Feb 10;90(2):301-7. doi: 10.1016/j.ajhg.2011.12.002. Epub 2012 Feb 2. Am J Hum Genet. 2012. PMID: 22305526 Free PMC article.
Defective cerebellar control of cortical plasticity in writer's cramp.
Hubsch C, Roze E, Popa T, Russo M, Balachandran A, Pradeep S, Mueller F, Brochard V, Quartarone A, Degos B, Vidailhet M, Kishore A, Meunier S. Hubsch C, et al. Among authors: brochard v. Brain. 2013 Jul;136(Pt 7):2050-62. doi: 10.1093/brain/awt147. Brain. 2013. PMID: 23801734 Free PMC article. Clinical Trial.
67 results