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Journal Abstract Search


553 related items for PubMed ID: 11014135

  • 1. [Hereditary dystonias].
    Hjermind LE, Sørensen SA, Werdelin LM.
    Ugeskr Laeger; 2000 Sep 18; 162(38):5066-70. PubMed ID: 11014135
    [Abstract] [Full Text] [Related]

  • 2. [Primary and secondary dystonias].
    Kerty E.
    Tidsskr Nor Laegeforen; 2008 Oct 09; 128(19):2206-9. PubMed ID: 18846146
    [Abstract] [Full Text] [Related]

  • 3. The monogenic primary dystonias.
    Müller U.
    Brain; 2009 Aug 09; 132(Pt 8):2005-25. PubMed ID: 19578124
    [Abstract] [Full Text] [Related]

  • 4. Early onset primary dystonia.
    Zorzi G, Zibordi F, Garavaglia B, Nardocci N.
    Eur J Paediatr Neurol; 2009 Nov 09; 13(6):488-92. PubMed ID: 19157930
    [Abstract] [Full Text] [Related]

  • 5. Genetics of dystonia.
    Fuchs T, Ozelius LJ.
    Semin Neurol; 2011 Nov 09; 31(5):441-8. PubMed ID: 22266882
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  • 7. Primary dystonia and dystonia-plus syndromes: clinical characteristics, diagnosis, and pathogenesis.
    Phukan J, Albanese A, Gasser T, Warner T.
    Lancet Neurol; 2011 Dec 09; 10(12):1074-85. PubMed ID: 22030388
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  • 11. Early-onset primary dystonia.
    Robottom BJ, Weiner WJ, Comella CL.
    Handb Clin Neurol; 2011 Dec 09; 100():465-79. PubMed ID: 21496603
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  • 12. Frequency and phenotypic variability of the GAG deletion of the DYT1 gene in an unselected group of patients with dystonia.
    Grundmann K, Laubis-Herrmann U, Bauer I, Dressler D, Vollmer-Haase J, Bauer P, Stuhrmann M, Schulte T, Schöls L, Topka H, Riess O.
    Arch Neurol; 2003 Sep 09; 60(9):1266-70. PubMed ID: 12975293
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  • 13. Dystonia and its disorders.
    Friedman J, Standaert DG.
    Neurol Clin; 2001 Aug 09; 19(3):681-705, vii. PubMed ID: 11532649
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  • 14. 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 09; 29(1):66-9. PubMed ID: 11528394
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  • 15. Dystonia--new advances in classification, genetics, pathophysiology and treatment.
    Skogseid IM.
    Acta Neurol Scand Suppl; 2014 Sep 09; (198):13-9. PubMed ID: 24588501
    [Abstract] [Full Text] [Related]

  • 16. [The varied etiologies of childhood-onset dystonia].
    Roubertie A, Rivier F, Humbertclaude V, Tuffery S, Cavalier L, Cheminal R, Coubes P, Echenne B.
    Rev Neurol (Paris); 2002 Apr 09; 158(4):413-24. PubMed ID: 11984483
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  • 17. Predominant dystonia with marked cerebellar atrophy: a rare phenotype in familial dystonia.
    Le Ber I, Clot F, Vercueil L, Camuzat A, Viémont M, Benamar N, De Liège P, Ouvrard-Hernandez AM, Pollak P, Stevanin G, Brice A, Dürr A.
    Neurology; 2006 Nov 28; 67(10):1769-73. PubMed ID: 17130408
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  • 18. Focal hand dystonia, mirror dystonia and motor overflow.
    Sitburana O, Jankovic J.
    J Neurol Sci; 2008 Mar 15; 266(1-2):31-3. PubMed ID: 17888455
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  • 19. Overview of primary monogenic dystonia.
    Spatola M, Wider C.
    Parkinsonism Relat Disord; 2012 Jan 15; 18 Suppl 1():S158-61. PubMed ID: 22166420
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  • 20. The clinical expression of primary dystonia.
    Albanese A.
    J Neurol; 2003 Oct 15; 250(10):1145-51. PubMed ID: 14586593
    [Abstract] [Full Text] [Related]


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