Vourc'h P - Search Results

1

Further development of biomarkers in amyotrophic lateral sclerosis.

Blasco H, Vourc'h P, Pradat PF, Gordon PH, Andres CR, Corcia P. Blasco H, et al. Expert Rev Mol Diagn. 2016 Aug;16(8):853-68. doi: 10.1080/14737159.2016.1199277. Epub 2016 Jun 20. Expert Rev Mol Diagn. 2016. PMID: 27275785 Review.

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

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

4

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.

5

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.

6

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

7

[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.

8

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

9

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

10

What was the set of ubiquitin and ubiquitin-like conjugating enzymes in the eukaryote common ancestor?

Michelle C, Vourc'h P, Mignon L, Andres CR. Michelle C, et al. J Mol Evol. 2009 Jun;68(6):616-28. doi: 10.1007/s00239-009-9225-6. Epub 2009 May 19. J Mol Evol. 2009. PMID: 19452197 Free PMC article.

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