Vourc'h P - Search Results

1

The Metabolic Disturbances of Motoneurons Exposed to Glutamate.

Madji Hounoum B, Blasco H, Coque E, Vourc'h P, Emond P, Corcia P, Andres CR, Raoul C, Mavel S. Madji Hounoum B, et al. Mol Neurobiol. 2018 Oct;55(10):7669-7676. doi: 10.1007/s12035-018-0945-8. Epub 2018 Feb 12. Mol Neurobiol. 2018. PMID: 29435916

2

No mutations in the coding region of the Rett syndrome gene MECP2 in 59 autistic patients.

Vourc'h P, Bienvenu T, Beldjord C, Chelly J, Barthélémy C, Müh JP, Andres C. Vourc'h P, et al. Eur J Hum Genet. 2001 Jul;9(7):556-8. doi: 10.1038/sj.ejhg.5200660. Eur J Hum Genet. 2001. PMID: 11464249

3

The oligodendrocyte-myelin glycoprotein gene is highly expressed during the late stages of myelination in the rat central nervous system.

Vourc'h P, Dessay S, Mbarek O, Marouillat Védrine S, Müh JP, Andres C. Vourc'h P, et al. Brain Res Dev Brain Res. 2003 Sep 10;144(2):159-68. doi: 10.1016/s0165-3806(03)00167-6. Brain Res Dev Brain Res. 2003. PMID: 12935913

4

Mutation screening and association study of the UBE2H gene on chromosome 7q32 in autistic disorder.

Vourc'h P, Martin I, Bonnet-Brilhault F, Marouillat S, Barthélémy C, Pierre Müh J, Andres C. Vourc'h P, et al. Psychiatr Genet. 2003 Dec;13(4):221-5. doi: 10.1097/00041444-200312000-00005. Psychiatr Genet. 2003. PMID: 14639049

5

Oligodendrocyte myelin glycoprotein (OMgp): evolution, structure and function.

Vourc'h P, Andres C. Vourc'h P, et al. Brain Res Brain Res Rev. 2004 May;45(2):115-24. doi: 10.1016/j.brainresrev.2004.01.003. Brain Res Brain Res Rev. 2004. PMID: 15145622 Review.

6

SMN1 gene, but not SMN2, is a risk factor for sporadic ALS.

Corcia P, Camu W, Halimi JM, Vourc'h P, Antar C, Vedrine S, Giraudeau B, de Toffol B, Andres CR; French ALS Study Group. Corcia P, et al. Neurology. 2006 Oct 10;67(7):1147-50. doi: 10.1212/01.wnl.0000233830.85206.1e. Epub 2006 Aug 23. Neurology. 2006. PMID: 16931506 Clinical Trial.

7

Transmission disequilibrium study of an oligodendrocyte and myelin glycoprotein gene allele in 431 families with an autistic proband.

Martin I, Gauthier J, D'Amelio M, Védrine S, Vourc'h P, Rouleau GA, Persico AM, Andres CR. Martin I, et al. Neurosci Res. 2007 Dec;59(4):426-30. doi: 10.1016/j.neures.2007.08.009. Epub 2007 Aug 19. Neurosci Res. 2007. PMID: 17897745

8

[Genetics of motor neuron disorders].

Corcia P, Praline J, Vourc'h P, Andres C. Corcia P, et al. Rev Neurol (Paris). 2008 Feb;164(2):115-30. doi: 10.1016/j.neurol.2007.10.002. Epub 2008 Feb 20. Rev Neurol (Paris). 2008. PMID: 18358870 Review. French.

9

Mutations of the ANG gene in French patients with sporadic amyotrophic lateral sclerosis.

Paubel A, Violette J, Amy M, Praline J, Meininger V, Camu W, Corcia P, Andres CR, Vourc'h P; French Amyotrophic Lateral Sclerosis (ALS) Study Group. Paubel A, et al. Arch Neurol. 2008 Oct;65(10):1333-6. doi: 10.1001/archneur.65.10.1333. Arch Neurol. 2008. PMID: 18852347

10

Haploinsufficiency of the GPD2 gene in a patient with nonsyndromic mental retardation.

Daoud H, Gruchy N, Constans JM, Moussaoui E, Saumureau S, Bayou N, Amy M, Védrine S, Vu PY, Rötig A, Laumonnier F, Vourc'h P, Andres CR, Leporrier N, Briault S. Daoud H, et al. Hum Genet. 2009 Jan;124(6):649-58. doi: 10.1007/s00439-008-0588-3. Epub 2008 Nov 16. Hum Genet. 2009. PMID: 19011903

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