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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

819 related items for PubMed ID: 18787576

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  • 4. [Hereditary ataxia-problems in the classification, genetics and genetic counseling].
    Bachmann H, Lössner J.
    Z Gesamte Inn Med; 1981 Jun 01; 36(11):387-93. PubMed ID: 7303765
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  • 5. Progressive cerebellar atrophy: hereditary ataxias and disorders with spinocerebellar degeneration.
    Wolf NI, Koenig M.
    Handb Clin Neurol; 2013 Jun 01; 113():1869-78. PubMed ID: 23622410
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  • 6. Classifications of hereditary ataxias. A critical overview.
    Campanella G, Filla A, De Michele G.
    Acta Neurol (Napoli); 1992 Jun 01; 14(4-6):408-19. PubMed ID: 1293984
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  • 11. [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 Jun 01; 147(12):798-808. PubMed ID: 1780608
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  • 12. [Ataxia and genetics].
    Berciano J.
    Med Clin (Barc); 2000 Jun 24; 115(4):135-6. PubMed ID: 10996884
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  • 16. [Friedreich ataxia--diagnosis after a decade. Differential diagnosis of inherited spinocerebellar ataxias].
    Vitaszil E, Jelencsik I, Szirmai I.
    Ideggyogy Sz; 2002 Nov 20; 55(11-12):382-93. PubMed ID: 12632799
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  • 17. Cerebellar ataxia in the eastern and southern parts of Norway.
    Koht J, Tallaksen CM.
    Acta Neurol Scand Suppl; 2007 Nov 20; 187():76-9. PubMed ID: 17419835
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