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PUBMED FOR HANDHELDS

Journal Abstract Search


547 related items for PubMed ID: 18759336

  • 1. 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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  • 3. Unusual familial presentation of epsilon-sarcoglycan gene mutation with falls and writer's cramp.
    Koukouni V, Valente EM, Cordivari C, Bhatia KP, Quinn NP.
    Mov Disord; 2008 Oct 15; 23(13):1913-5. PubMed ID: 18702114
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  • 4. Cortical excitability in DYT-11 positive myoclonus dystonia.
    Sabine MeunierINSERM, U731, Paris, France., George Lourenco, Roze E, Apartis E, Trocello JM, Marie Vidailhet.
    Mov Disord; 2008 Apr 15; 23(5):761-4. PubMed ID: 18265016
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  • 5. 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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  • 6. Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome.
    Zimprich A, Grabowski M, Asmus F, Naumann M, Berg D, Bertram M, Scheidtmann K, Kern P, Winkelmann J, Müller-Myhsok B, Riedel L, Bauer M, Müller T, Castro M, Meitinger T, Strom TM, Gasser T.
    Nat Genet; 2001 Sep 15; 29(1):66-9. PubMed ID: 11528394
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  • 8. The neurophysiological features of myoclonus-dystonia and differentiation from other dystonias.
    Popa T, Milani P, Richard A, Hubsch C, Brochard V, Tranchant C, Sadnicka A, Rothwell J, Vidailhet M, Meunier S, Roze E.
    JAMA Neurol; 2014 May 15; 71(5):612-9. PubMed ID: 24638021
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  • 10. Clinical differentiation of genetically proven benign hereditary chorea and myoclonus-dystonia.
    Asmus F, Devlin A, Munz M, Zimprich A, Gasser T, Chinnery PF.
    Mov Disord; 2007 Oct 31; 22(14):2104-9. PubMed ID: 17702043
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  • 11. 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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  • 12. Normal cortical excitability in Myoclonus-Dystonia--a TMS study.
    van der Salm SM, van Rootselaar AF, Foncke EM, Koelman JH, Bour LJ, Bhatia KP, Rothwell JC, Tijssen MA.
    Exp Neurol; 2009 Apr 25; 216(2):300-5. PubMed ID: 19118553
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  • 14. Cortical reflex myoclonus in Rett syndrome.
    Guerrini R, Bonanni P, Parmeggiani L, Santucci M, Parmeggiani A, Sartucci F.
    Ann Neurol; 1998 Apr 25; 43(4):472-9. PubMed ID: 9546328
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  • 18. Difference in intracortical inhibition of the motor cortex between cortical myoclonus and focal hand dystonia.
    Hanajima R, Okabe S, Terao Y, Furubayashi T, Arai N, Inomata-Terada S, Hamada M, Yugeta A, Ugawa Y.
    Clin Neurophysiol; 2008 Jun 25; 119(6):1400-7. PubMed ID: 18387338
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