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Journal Abstract Search

600 related items for PubMed ID: 18362280

  • 1. Myoclonus-dystonia: clinical and electrophysiologic pattern related to SGCE mutations.
    Roze E, Apartis E, Clot F, Dorison N, Thobois S, Guyant-Marechal L, Tranchant C, Damier P, Doummar D, Bahi-Buisson N, André-Obadia N, Maltete D, Echaniz-Laguna A, Pereon Y, Beaugendre Y, Dupont S, De Greslan T, Jedynak CP, Ponsot G, Dussaule JC, Brice A, Dürr A, Vidailhet M.
    Neurology; 2008 Mar 25; 70(13):1010-6. PubMed ID: 18362280
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  • 2. "Jerky" dystonia in children: spectrum of phenotypes and genetic testing.
    Asmus F, Langseth A, Doherty E, Nestor T, Munz M, Gasser T, Lynch T, King MD.
    Mov Disord; 2009 Apr 15; 24(5):702-9. PubMed ID: 19117362
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  • 3. Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromes.
    Tezenas du Montcel S, Clot F, Vidailhet M, Roze E, Damier P, Jedynak CP, Camuzat A, Lagueny A, Vercueil L, Doummar D, Guyant-Maréchal L, Houeto JL, Ponsot G, Thobois S, Cournelle MA, Durr A, Durif F, Echenne B, Hannequin D, Tranchant C, Brice A, French Dystonia Network.
    J Med Genet; 2006 May 15; 43(5):394-400. PubMed ID: 16227522
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  • 4. Myoclonus-dystonia syndrome: clinical presentation, disease course, and genetic features in 11 families.
    Nardocci N, Zorzi G, Barzaghi C, Zibordi F, Ciano C, Ghezzi D, Garavaglia B.
    Mov Disord; 2008 Jan 15; 23(1):28-34. PubMed ID: 17853490
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  • 9. Myoclonus-dystonia, obsessive-compulsive disorder, and alcohol dependence in SGCE mutation carriers.
    Hess CW, Raymond D, Aguiar Pde C, Frucht S, Shriberg J, Heiman GA, Kurlan R, Klein C, Bressman SB, Ozelius LJ, Saunders-Pullman R.
    Neurology; 2007 Feb 13; 68(7):522-4. PubMed ID: 17296918
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  • 16. Phenotypic spectrum and sex effects in eleven myoclonus-dystonia families with epsilon-sarcoglycan mutations.
    Raymond D, Saunders-Pullman R, de Carvalho Aguiar P, Schule B, Kock N, Friedman J, Harris J, Ford B, Frucht S, Heiman GA, Jennings D, Doheny D, Brin MF, de Leon Brin D, Multhaupt-Buell T, Lang AE, Kurlan R, Klein C, Ozelius L, Bressman S.
    Mov Disord; 2008 Mar 15; 23(4):588-92. PubMed ID: 18175340
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  • 17. A neurophysiological study of myoclonus in patients with DYT11 myoclonus-dystonia syndrome.
    Marelli C, Canafoglia L, Zibordi F, Ciano C, Visani E, Zorzi G, Garavaglia B, Barzaghi C, Albanese A, Soliveri P, Leone M, Panzica F, Scaioli V, Pincherle A, Nardocci N, Franceschetti S.
    Mov Disord; 2008 Oct 30; 23(14):2041-8. PubMed ID: 18759336
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  • 18. Myoclonus in fraternal twin toddlers: a French family with a novel mutation in the SGCE gene.
    Thümmler S, Giuliano F, Pincemaille O, Saugier-Veber P, Perelman S.
    Eur J Paediatr Neurol; 2009 Nov 30; 13(6):559-61. PubMed ID: 19147379
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  • 19. Clinical and genetic features of myoclonus-dystonia in 3 cases: a video presentation.
    Kock N, Kasten M, Schüle B, Hedrich K, Wiegers K, Kabakci K, Hagenah J, Pramstaller PP, Nitschke MF, Münchau A, Sperner J, Klein C.
    Mov Disord; 2004 Feb 30; 19(2):231-4. PubMed ID: 14978685
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  • 20. Phenotype-genotype correlation in Dutch patients with myoclonus-dystonia.
    Gerrits MC, Foncke EM, de Haan R, Hedrich K, van de Leemput YL, Baas F, Ozelius LJ, Speelman JD, Klein C, Tijssen MA.
    Neurology; 2006 Mar 14; 66(5):759-61. PubMed ID: 16534121
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