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Journal Abstract Search

268 related items for PubMed ID: 15356687

  • 1. [Genetics in movement disorders--dystonia, tremor and chorea].
    Dietrichs E, Tallaksen CM.
    Tidsskr Nor Laegeforen; 2004 Sep 09; 124(17):2236-7. PubMed ID: 15356687
    [Abstract] [Full Text] [Related]

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

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

  • 4. Genetics of dystonia.
    Fuchs T, Ozelius LJ.
    Semin Neurol; 2011 Nov 09; 31(5):441-8. PubMed ID: 22266882
    [Abstract] [Full Text] [Related]

  • 5. Inherited movement disorders.
    Harding AE.
    Baillieres Clin Neurol; 1994 Aug 09; 3(2):259-79. PubMed ID: 7952847
    [Abstract] [Full Text] [Related]

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

  • 7. The Huntington's disease-like syndromes: what to consider in patients with a negative Huntington's disease gene test.
    Schneider SA, Walker RH, Bhatia KP.
    Nat Clin Pract Neurol; 2007 Sep 18; 3(9):517-25. PubMed ID: 17805246
    [Abstract] [Full Text] [Related]

  • 8. [Presymptomatic diagnosis in genetics: the model of Huntington disease].
    Feingold J, Dürr A.
    Pathol Biol (Paris); 1997 Mar 18; 45(3):209-12. PubMed ID: 9296065
    [Abstract] [Full Text] [Related]

  • 9. 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 18; 43(5):394-400. PubMed ID: 16227522
    [Abstract] [Full Text] [Related]

  • 10. [The genetics of movement disorders--spinocerebellar degenerations].
    Tallaksen CM, Dietrichs E.
    Tidsskr Nor Laegeforen; 2004 Sep 09; 124(17):2233-5. PubMed ID: 15356686
    [Abstract] [Full Text] [Related]

  • 11. [Genetic counseling on a molecular basis for Huntington's chorea].
    Cassiman JJ.
    J Genet Hum; 1989 Jan 09; 37(1):13-24. PubMed ID: 2565951
    [Abstract] [Full Text] [Related]

  • 12. [Essential tremor].
    Dietrichs E, Kvikstad V.
    Tidsskr Nor Laegeforen; 2008 Oct 09; 128(19):2210-3. PubMed ID: 18846147
    [Abstract] [Full Text] [Related]

  • 13. 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. Movement disorders and alcohol misuse.
    Hess CW, Saunders-Pullman R.
    Addict Biol; 2006 Jun 28; 11(2):117-25. PubMed ID: 16800824
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