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Journal Abstract Search

475 related items for PubMed ID: 17715286

  • 1. Spinocerebellar ataxia type 2 in a Turkish family.
    Dirik E, Yiş U, Başak N, Soydan E, Hüdaoğlu O, Ozgönül F.
    J Child Neurol; 2007 Jul; 22(7):891-4. PubMed ID: 17715286
    [Abstract] [Full Text] [Related]

  • 2. Dentatorubral pallidoluysian atrophy in a Turkish family.
    Yiş U, Dirik E, Gündoğdu-Eken A, Başak AN.
    Turk J Pediatr; 2009 Jul; 51(6):610-2. PubMed ID: 20196398
    [Abstract] [Full Text] [Related]

  • 3. Spinocerebellar ataxia type 2 (SCA 2) in an infant with extreme CAG repeat expansion.
    Babovic-Vuksanovic D, Snow K, Patterson MC, Michels VV.
    Am J Med Genet; 1998 Oct 12; 79(5):383-7. PubMed ID: 9779806
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  • 4. Phenotype variability in spinocerebellar ataxia type 2: a longitudinal family survey and a case featuring an unusual benign course of disease.
    Hering S, Achmüller C, Köhler A, Poewe W, Schneider R, Boesch SM.
    Mov Disord; 2009 Apr 15; 24(5):774-7. PubMed ID: 19224595
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  • 5. Clinical and genetic findings in Finnish ataxia patients with the spinocerebellar ataxia 8 repeat expansion.
    Juvonen V, Hietala M, Päivärinta M, Rantamäki M, Hakamies L, Kaakkola S, Vierimaa O, Penttinen M, Savontaus ML.
    Ann Neurol; 2000 Sep 15; 48(3):354-61. PubMed ID: 10976642
    [Abstract] [Full Text] [Related]

  • 6. [Spinocerebellar ataxia type 7: clinical and molecular genetic analysis of a Mexican family].
    Rolón Lacarriere O, Rasmussen Almaraz A, Hernández Cruz H, Carranza del Río J, González Cruz M, Gutiérrez Moctezuma J.
    Rev Neurol; 2000 Sep 15; 38(8):736-40. PubMed ID: 15122543
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  • 13. The parkinsonian phenotype of spinocerebellar ataxia type 2.
    Lu CS, Wu Chou YH, Kuo PC, Chang HC, Weng YH.
    Arch Neurol; 2004 Jan 15; 61(1):35-8. PubMed ID: 14732617
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  • 14. Refinement of the spinocerebellar ataxia type 4 locus in a large German family and exclusion of CAG repeat expansions in this region.
    Hellenbroich Y, Bubel S, Pawlack H, Opitz S, Vieregge P, Schwinger E, Zühlke C.
    J Neurol; 2003 Jun 15; 250(6):668-71. PubMed ID: 12796826
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  • 15. Spinocerebellar ataxia type 17: extension of phenotype with putaminal rim hyperintensity on magnetic resonance imaging.
    Loy CT, Sweeney MG, Davis MB, Wills AJ, Sawle GV, Lees AJ, Tabrizi SJ.
    Mov Disord; 2005 Nov 15; 20(11):1521-3. PubMed ID: 16037935
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  • 17. Expanded ATXN2 CAG repeat size in ALS identifies genetic overlap between ALS and SCA2.
    Van Damme P, Veldink JH, van Blitterswijk M, Corveleyn A, van Vught PW, Thijs V, Dubois B, Matthijs G, van den Berg LH, Robberecht W.
    Neurology; 2011 Jun 14; 76(24):2066-72. PubMed ID: 21562247
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  • 18. Mapping of autosomal dominant cerebellar ataxia without the pathogenic PPP2R2B mutation to the locus for spinocerebellar ataxia 12.
    Sato K, Yabe I, Fukuda Y, Soma H, Nakahara Y, Tsuji S, Sasaki H.
    Arch Neurol; 2010 Oct 14; 67(10):1257-62. PubMed ID: 20937954
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  • 19. Schizophrenia in a patient with spinocerebellar ataxia 2: coincidence of two disorders or a neurodegenerative disease presenting with psychosis?
    Rottnek M, Riggio S, Byne W, Sano M, Margolis RL, Walker RH.
    Am J Psychiatry; 2008 Aug 14; 165(8):964-7. PubMed ID: 18676601
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