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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

700 related items for PubMed ID: 19117362

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  • 2. 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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  • 7. Large deletions account for an increasing number of mutations in SGCE.
    Han F, Racacho L, Yang H, Read T, Suchowersky O, Lang AE, Grimes DA, Bulman DE.
    Mov Disord; 2008 Feb 15; 23(3):456-60. PubMed ID: 18098280
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  • 11. 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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  • 15. 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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  • 17. Inherited myoclonus-dystonia and epilepsy: further evidence of an association?
    O'Riordan S, Ozelius LJ, de Carvalho Aguiar P, Hutchinson M, King M, Lynch T.
    Mov Disord; 2004 Dec 13; 19(12):1456-9. PubMed ID: 15389977
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  • 20. A novel mutation of the epsilon-sarcoglycan gene in a Chinese family with myoclonus-dystonia syndrome.
    Chen XP, Zhang YW, Zhang SS, Chen Q, Burgunder JM, Wu SH, Yang Y, Luo ZM, Shang HF.
    Mov Disord; 2008 Jul 30; 23(10):1472-5. PubMed ID: 18581468
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