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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

474 related items for PubMed ID: 17204042

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  • 3. Autosomal recessive cerebellar ataxias.
    Palau F, Espinós C.
    Orphanet J Rare Dis; 2006 Nov 17; 1():47. PubMed ID: 17112370
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  • 6. [Genetic diagnosis, classification and clinical hereditary ataxia disease entities].
    Schöls L, Riess O, Amoiridis G, Riess A, Przuntek H, Epplen JT.
    Fortschr Neurol Psychiatr; 1997 Feb 17; 65(2):79-89. PubMed ID: 9157050
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  • 7. Progressive cerebellar atrophy: hereditary ataxias and disorders with spinocerebellar degeneration.
    Wolf NI, Koenig M.
    Handb Clin Neurol; 2013 Feb 17; 113():1869-78. PubMed ID: 23622410
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  • 9. [Clinical polymorphism and genetic heterogeneity of hereditary spastic ataxia].
    Dadali EL, Illarioshkin SN, Markova ED, Ivanova-Smolenskaia IA.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1992 Feb 17; 92(4):10-3. PubMed ID: 1333696
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  • 10. Spinocerebellar degeneration.
    Phanthumchinda K, Srikiatkachorn A.
    J Med Assoc Thai; 1991 Feb 17; 74(2):71-9. PubMed ID: 2056261
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  • 14. Clinical spectrum of early onset cerebellar ataxia with retained tendon reflexes: an autosomal recessive ataxia not to be missed.
    Pedroso JL, Braga-Neto P, Ricarte IF, Albuquerque MV, Barsottini OG.
    Arq Neuropsiquiatr; 2013 Jun 17; 71(6):345-8. PubMed ID: 23828538
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  • 17. Pure cerebello-olivary degeneration of Marie, Foix, and Alajouanine presenting with progressive cerebellar ataxia, cognitive decline, and chorea.
    Fox SH, Nieves A, Bergeron C, Lang AE.
    Mov Disord; 2003 Dec 17; 18(12):1550-4. PubMed ID: 14673899
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