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Journal Abstract Search

344 related items for PubMed ID: 17419835

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  • 2. [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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  • 4. Clinical and genetic epidemiological study of 16q22.1-linked autosomal dominant cerebellar ataxia in western Japan.
    Hayashi M, Adachi Y, Mori M, Nakano T, Nakashima K.
    Acta Neurol Scand; 2007 Aug 24; 116(2):123-7. PubMed ID: 17661799
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  • 8. Autosomal recessive cerebellar ataxias.
    Palau F, Espinós C.
    Orphanet J Rare Dis; 2006 Nov 17; 1():47. PubMed ID: 17112370
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  • 9. [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 Nov 17; 147(12):798-808. PubMed ID: 1780608
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  • 10. 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 17; 111(6):391-9. PubMed ID: 15876341
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  • 16. [Recessive hereditary ataxia with early onset. Clinical study of 27 cases].
    Serlenga L, Trizio M, Pozio G, Oteri G, Caldarazzo M.
    Riv Neurol; 1987 Jun 17; 57(5):285-9. PubMed ID: 3445070
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  • 17. Prevalence of inherited ataxias in the province of Padua, Italy.
    Zortea M, Armani M, Pastorello E, Nunez GF, Lombardi S, Tonello S, Rigoni MT, Zuliani L, Mostacciuolo ML, Gellera C, Di Donato S, Trevisan CP.
    Neuroepidemiology; 2004 Jun 17; 23(6):275-80. PubMed ID: 15297793
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  • 18. 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 17; 63(4):553-5. PubMed ID: 16606768
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  • 19. An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus?
    Waters MF, Fee D, Figueroa KP, Nolte D, Müller U, Advincula J, Coon H, Evidente VG, Pulst SM.
    Neurology; 2005 Oct 11; 65(7):1111-3. PubMed ID: 16135769
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  • 20. Analysis of spinocerebellar ataxia types 1, 2, 3, and 6, dentatorubral-pallidoluysian atrophy, and Friedreich's ataxia genes in spinocerebellar ataxia patients in the UK.
    Leggo J, Dalton A, Morrison PJ, Dodge A, Connarty M, Kotze MJ, Rubinsztein DC.
    J Med Genet; 1997 Dec 11; 34(12):982-5. PubMed ID: 9429138
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