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Journal Abstract Search

322 related items for PubMed ID: 1293985

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  • 4. [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; 147(12):798-808. PubMed ID: 1780608
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  • 6. [Hereditary ataxias].
    Tallaksen CM.
    Tidsskr Nor Laegeforen; 2008 Sep 11; 128(17):1977-80. PubMed ID: 18787576
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  • 9. Cerebellar ataxia in the eastern and southern parts of Norway.
    Koht J, Tallaksen CM.
    Acta Neurol Scand Suppl; 2007 Sep 11; 187():76-9. PubMed ID: 17419835
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  • 10. Early onset cerebellar ataxia with retained tendon reflexes: a clinical and genetic study of a disorder distinct from Friedreich's ataxia.
    Harding AE.
    J Neurol Neurosurg Psychiatry; 1981 Jun 11; 44(6):503-8. PubMed ID: 7276963
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  • 11. Classifications of hereditary ataxias. A critical overview.
    Campanella G, Filla A, De Michele G.
    Acta Neurol (Napoli); 1992 Jun 11; 14(4-6):408-19. PubMed ID: 1293984
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  • 12. Autosomal recessive cerebellar ataxias.
    Palau F, Espinós C.
    Orphanet J Rare Dis; 2006 Nov 17; 1():47. PubMed ID: 17112370
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  • 13. [Friedrich's ataxia: clinical difficulties and genetic possibilities].
    van de Warrenburg BP, Knoers NV, Kremer HP.
    Ned Tijdschr Geneeskd; 2002 Sep 07; 146(36):1669-72. PubMed ID: 12244768
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  • 15. [Eye movement disorders in hereditary degenerative ataxia. Electro-oculographic study of 11 cases].
    Serlenga L, Falco F, Castaldo V, Caldarazzo M, Federici A.
    Acta Neurol (Napoli); 1992 Sep 07; 14(4-6):440-50. PubMed ID: 1293987
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  • 19. Late-onset Friedreich ataxia: phenotypic analysis, magnetic resonance imaging findings, and review of the literature.
    Bhidayasiri R, Perlman SL, Pulst SM, Geschwind DH.
    Arch Neurol; 2005 Dec 07; 62(12):1865-9. PubMed ID: 16344344
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