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Page 1
Ovarian failure related to eukaryotic initiation factor 2B mutations.
Fogli A, Rodriguez D, Eymard-Pierre E, Bouhour F, Labauge P, Meaney BF, Zeesman S, Kaneski CR, Schiffmann R, Boespflug-Tanguy O. Fogli A, et al. Among authors: labauge p. Am J Hum Genet. 2003 Jun;72(6):1544-50. doi: 10.1086/375404. Epub 2003 Apr 21. Am J Hum Genet. 2003. PMID: 12707859 Free PMC article.
Mutations within the MGC4607 gene cause cerebral cavernous malformations.
Denier C, Goutagny S, Labauge P, Krivosic V, Arnoult M, Cousin A, Benabid AL, Comoy J, Frerebeau P, Gilbert B, Houtteville JP, Jan M, Lapierre F, Loiseau H, Menei P, Mercier P, Moreau JJ, Nivelon-Chevallier A, Parker F, Redondo AM, Scarabin JM, Tremoulet M, Zerah M, Maciazek J, Tournier-Lasserve E; Société Française de Neurochirurgie. Denier C, et al. Among authors: labauge p. Am J Hum Genet. 2004 Feb;74(2):326-37. doi: 10.1086/381718. Epub 2004 Jan 22. Am J Hum Genet. 2004. PMID: 14740320 Free PMC article.
Mutations within the programmed cell death 10 gene cause cerebral cavernous malformations.
Bergametti F, Denier C, Labauge P, Arnoult M, Boetto S, Clanet M, Coubes P, Echenne B, Ibrahim R, Irthum B, Jacquet G, Lonjon M, Moreau JJ, Neau JP, Parker F, Tremoulet M, Tournier-Lasserve E; Société Française de Neurochirurgie. Bergametti F, et al. Among authors: labauge p. Am J Hum Genet. 2005 Jan;76(1):42-51. doi: 10.1086/426952. Epub 2004 Nov 12. Am J Hum Genet. 2005. PMID: 15543491 Free PMC article.
Dominant form of vanishing white matter-like leukoencephalopathy.
Labauge P, Fogli A, Castelnovo G, Le Bayon A, Horzinski L, Nicoli F, Cozzone P, Pagès M, Briere C, Marty-Double C, Delhaume O, Gelot A, Boespflug-Tanguy O, Rodriguez D. Labauge P, et al. Ann Neurol. 2005 Oct;58(4):634-9. doi: 10.1002/ana.20573. Ann Neurol. 2005. PMID: 16047349
Genes involved in leukodystrophies: a glance at glial functions.
Boespflug-Tanguy O, Labauge P, Fogli A, Vaurs-Barriere C. Boespflug-Tanguy O, et al. Among authors: labauge p. Curr Neurol Neurosci Rep. 2008 May;8(3):217-29. doi: 10.1007/s11910-008-0034-x. Curr Neurol Neurosci Rep. 2008. PMID: 18541117 Review.
[Genetic demyelinating diseases].
Labauge P, Boespflug-Tanguy O. Labauge P, et al. Presse Med. 2010 Mar;39(3):363-70. doi: 10.1016/j.lpm.2009.11.011. Epub 2010 Feb 18. Presse Med. 2010. PMID: 20167452 French.
469 results