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Journal Abstract Search

247 related items for PubMed ID: 10996881

  • 1. [Distribution of dominant hereditary ataxias and Friedreich's ataxia in the Spanish population].
    Mayo Cabrero D, Hernández Cristóbal J, Cantarero Duque S, Martínez Delgado B, Urioste Azcorra M, Robledo Batanero M, García-Ruiz Espiga P, Benítez Ortiz J.
    Med Clin (Barc); 2000 Jun 24; 115(4):121-5. PubMed ID: 10996881
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  • 8. Frequency analysis of autosomal dominant cerebellar ataxias in Taiwanese patients and clinical and molecular characterization of spinocerebellar ataxia type 6.
    Soong B W, Lu Y C, Choo K B, Lee H Y.
    Arch Neurol; 2001 Jul 24; 58(7):1105-9. PubMed ID: 11448300
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  • 11. Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia families.
    Moseley ML, Benzow KA, Schut LJ, Bird TD, Gomez CM, Barkhaus PE, Blindauer KA, Labuda M, Pandolfo M, Koob MD, Ranum LP.
    Neurology; 1998 Dec 24; 51(6):1666-71. PubMed ID: 9855520
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  • 15. Quantification of circulating plasma DNA in Friedreich's ataxia and spinocerebellar ataxia types 2 and 12.
    Swarup V, Srivastava AK, Padma MV, Rajeswari MR.
    DNA Cell Biol; 2011 Jun 24; 30(6):389-94. PubMed ID: 21329459
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  • 16. 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 24; 39(1):80-5. PubMed ID: 17159980
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  • 18. SCA-LSVD: a repeat-oriented locus-specific variation database for genotype to phenotype correlations in spinocerebellar ataxias.
    Faruq M, Scaria V, Singh I, Tyagi S, Srivastava AK, Mukerji M.
    Hum Mutat; 2009 Jul 24; 30(7):1037-42. PubMed ID: 19370769
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