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Journal Abstract Search

354 related items for PubMed ID: 15236416

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  • 4. [Advance in research on spinocerebellar ataxia 17].
    Zhang J, Gu W.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Feb; 31(1):44-7. PubMed ID: 24510561
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  • 6. Focal dystonia as a presenting sign of spinocerebellar ataxia 17.
    Hagenah JM, Zühlke C, Hellenbroich Y, Heide W, Klein C.
    Mov Disord; 2004 Feb; 19(2):217-20. PubMed ID: 14978680
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  • 8. Molecular analysis of spinocerebellar ataxia trinucleotide repeat behavior in normal individuals of a Brazilian population.
    de Vargas Wolfgramm E, de Carvalho FM, De Nadai Sartori MP, Spagnol Perrone AM, de Paula F, Louro ID.
    J Neurol Sci; 2008 Jun 15; 269(1-2):113-7. PubMed ID: 18262566
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  • 11. SCA17 homozygote showing Huntington's disease-like phenotype.
    Toyoshima Y, Yamada M, Onodera O, Shimohata M, Inenaga C, Fujita N, Morita M, Tsuji S, Takahashi H.
    Ann Neurol; 2004 Feb 15; 55(2):281-6. PubMed ID: 14755733
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  • 13. Huntington disease and Huntington disease-like in a case series from Brazil.
    Castilhos RM, Souza AF, Furtado GV, Gheno TC, Silva AL, Vargas FR, Lima MA, Barsottini O, Pedroso JL, Godeiro C, Salarini D, Pereira ET, Lin K, Toralles MB, Saute JA, Rieder CR, Quintas M, Sequeiros J, Alonso I, Saraiva-Pereira ML, Jardim LB.
    Clin Genet; 2014 Oct 15; 86(4):373-7. PubMed ID: 24102565
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  • 14. Meiotic CAG repeat instability in spinocerebellar ataxia type 6: maternally transmitted elongation in a presumed sporadic case.
    Lindquist SG, Nørremølle A, Hjermind LE, Hasholt L, Nielsen JE.
    J Neurol Sci; 2006 Feb 15; 241(1-2):95-8. PubMed ID: 16310805
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  • 16. Clinical and genetic analysis of 29 Brazilian patients with Huntington's disease-like phenotype.
    Rodrigues GR, Walker RH, Bader B, Danek A, Brice A, Cazeneuve C, Russaouen O, Lopes-Cendes I, Marques W, Tumas V.
    Arq Neuropsiquiatr; 2011 Jun 15; 69(3):419-23. PubMed ID: 21755114
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  • 19. Genotype/phenotype correlation in a SCA1 family: anticipation without CAG expansion.
    Bauer PO, Matoska V, Zumrova A, Boday A, Doi H, Marikova T, Goetz P.
    J Appl Genet; 2005 Jun 15; 46(3):325-8. PubMed ID: 16110192
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  • 20. Genetic and clinical analysis of spinocerebellar ataxia type 8 repeat expansion in Yugoslavia.
    Topisirovic I, Dragasevic N, Savic D, Ristic A, Keckarevic M, Keckarevic D, Culjkovic B, Petrovic I, Romac S, Kostic VS.
    Clin Genet; 2002 Oct 15; 62(4):321-4. PubMed ID: 12372061
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