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Journal Abstract Search

371 related items for PubMed ID: 16606768

  • 1. Cerebellar ataxia with spasmodic cough: a new form of dominant ataxia.
    Coutinho P, Cruz VT, Tuna A, Silva SE, Guimarães J.
    Arch Neurol; 2006 Apr; 63(4):553-5. PubMed ID: 16606768
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  • 2. 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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  • 4. Mutations in SYNE1 lead to a newly discovered form of autosomal recessive cerebellar ataxia.
    Gros-Louis F, Dupré N, Dion P, Fox MA, Laurent S, Verreault S, Sanes JR, Bouchard JP, Rouleau GA.
    Nat Genet; 2007 Jan 28; 39(1):80-5. PubMed ID: 17159980
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  • 7. Clinical and genetic study of autosomal recessive cerebellar ataxia type 1.
    Dupré N, Gros-Louis F, Chrestian N, Verreault S, Brunet D, de Verteuil D, Brais B, Bouchard JP, Rouleau GA.
    Ann Neurol; 2007 Jul 28; 62(1):93-8. PubMed ID: 17503513
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  • 8. [Clinical and genetic analysis of 188 families with spinocerebellar degeneration. Friedreich's disease and P. Marie's hereditary ataxias].
    Ben Hamida M, Attia-Romdhane N, Triki CH, Oueslati S, Hentati F.
    Rev Neurol (Paris); 1991 Jul 28; 147(12):798-808. PubMed ID: 1780608
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  • 11. Early-onset progressive ataxia associated with the first CACNA1A mutation identified within the I-II loop.
    Cricchi F, Di Lorenzo C, Grieco GS, Rengo C, Cardinale A, Racaniello M, Santorelli FM, Nappi G, Pierelli F, Casali C.
    J Neurol Sci; 2007 Mar 15; 254(1-2):69-71. PubMed ID: 17292920
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  • 12. Genetic heterogeneity of autosomal dominant nonprogressive congenital ataxia.
    Jen JC, Lee H, Cha YH, Nelson SF, Baloh RW.
    Neurology; 2006 Nov 14; 67(9):1704-6. PubMed ID: 17101914
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  • 15. Degree of cerebellar ataxia correlates with three-dimensional mri-based cerebellar volume in pure cerebellar degeneration.
    Richter S, Dimitrova A, Maschke M, Gizewski E, Beck A, Aurich V, Timmann D.
    Eur Neurol; 2005 Nov 14; 54(1):23-7. PubMed ID: 16088175
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  • 17. [Hereditary ataxias].
    Tallaksen CM.
    Tidsskr Nor Laegeforen; 2008 Sep 11; 128(17):1977-80. PubMed ID: 18787576
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  • 18. Autosomal dominant cerebellar ataxias in Spain: molecular and clinical correlations, prevalence estimation and survival analysis.
    Infante J, Combarros O, Volpini V, Corral J, Llorca J, Berciano J.
    Acta Neurol Scand; 2005 Jun 11; 111(6):391-9. PubMed ID: 15876341
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  • 19. [Does the ataxo-choreic form of DRPLA exist in Europe? Search of mutation in 120 families].
    Dubourg O, Dürr A, Chneiweiss H, Stevanin G, Cancel G, Penet C, Agid Y, Brice A.
    Rev Neurol (Paris); 1995 Nov 11; 151(11):657-60. PubMed ID: 8745629
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  • 20. Clinical features of chromosome 16q22.1 linked autosomal dominant cerebellar ataxia in Japanese.
    Onodera Y, Aoki M, Mizuno H, Warita H, Shiga Y, Itoyama Y.
    Neurology; 2006 Oct 10; 67(7):1300-2. PubMed ID: 17030774
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