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Identity by descent fine mapping of familial adult myoclonus epilepsy (FAME) to 2p11.2-2q11.2.
Henden L, Freytag S, Afawi Z, Baldassari S, Berkovic SF, Bisulli F, Canafoglia L, Casari G, Crompton DE, Depienne C, Gecz J, Guerrini R, Helbig I, Hirsch E, Keren B, Klein KM, Labauge P, LeGuern E, Licchetta L, Mei D, Nava C, Pippucci T, Rudolf G, Scheffer IE, Striano P, Tinuper P, Zara F, Corbett M, Bahlo M. Henden L, et al. Among authors: labauge p. Hum Genet. 2016 Oct;135(10):1117-25. doi: 10.1007/s00439-016-1700-8. Epub 2016 Jul 1. Hum Genet. 2016. PMID: 27368338
Identical genetic locus for Baltic and Mediterranean myoclonus.
Malafosse A, Lehesjoki AE, Genton P, Labauge P, Durand G, Tassinari CA, Dravet C, Michelucci R, de la Chapelle A. Malafosse A, et al. Among authors: labauge p. Lancet. 1992 May 2;339(8801):1080-1. doi: 10.1016/0140-6736(92)90667-r. Lancet. 1992. PMID: 1349105
Lafora disease is not linked to the Unverricht-Lundborg locus.
Labauge P, Beck C, Bellet H, Coquillat G, Vespignani H, Dulac O, Gilgenkrantz S, Dravet C, Genton P, Pellissier JF, et al. Labauge P, et al. Am J Med Genet. 1995 Feb 27;60(1):80-4. doi: 10.1002/ajmg.1320600114. Am J Med Genet. 1995. PMID: 7485240
Genetic heterogeneity of familial hemiplegic migraine.
Joutel A, Ducros A, Vahedi K, Labauge P, Delrieu O, Pinsard N, Mancini J, Ponsot G, Gouttière F, Gastaut JL, et al. Joutel A, et al. Among authors: labauge p. Am J Hum Genet. 1994 Dec;55(6):1166-72. Am J Hum Genet. 1994. PMID: 7977376 Free PMC article.
A gene for familial hemiplegic migraine maps to chromosome 19.
Joutel A, Bousser MG, Biousse V, Labauge P, Chabriat H, Nibbio A, Maciazek J, Meyer B, Bach MA, Weissenbach J, et al. Joutel A, et al. Among authors: labauge p. Nat Genet. 1993 Sep;5(1):40-5. doi: 10.1038/ng0993-40. Nat Genet. 1993. PMID: 8220421
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.
459 results