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Journal Abstract Search

191 related items for PubMed ID: 3504245

  • 1. Ramsay Hunt syndrome and coeliac disease: a new association?
    Lu CS, Thompson PD, Quinn NP, Parkes JD, Marsden CD.
    Mov Disord; 1986; 1(3):209-19. PubMed ID: 3504245
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  • 2. [Familial olivo-ponto-cerebellar atrophy with myoclonus. Limits of cerebellar myoclonic dyssynergia (Ramsay-Hunt syndrome)].
    Bonduelle M, Escourolle R, Bouygues P, Lormeau G, Gray F.
    Rev Neurol (Paris); 1976 Feb; 132(2):113-24. PubMed ID: 973068
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  • 3. Oculomotor abnormalities in Dyssynergia cerebellaris myoclonica.
    Wiest G, Mueller C, Wessely P, Steinhoff N, Trattnig S, Deecke L.
    Acta Otolaryngol Suppl; 1995 Feb; 520 Pt 2():392-4. PubMed ID: 8749170
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  • 5. [Myoclonic cerebellar dyssynergia (Ramsay-Hunt syndrome) and cerebellar telangiectasia].
    Gray F, Signoret JL, Colin R, Hauw JJ, Escourolle R, Lhermitte F.
    Rev Neurol (Paris); 1986 Feb; 142(1):29-33. PubMed ID: 3085192
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  • 11. Dyssynergia cerebellaris myoclonica (Ramsay Hunt syndrome): a condition unrelated to mitochondrial encephalomyopathies.
    Tassinari CA, Michelucci R, Genton P, Pellissier JF, Roger J.
    J Neurol Neurosurg Psychiatry; 1989 Feb; 52(2):262-5. PubMed ID: 2703843
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  • 14. Action myoclonus, Ramsay Hunt syndrome, and other cerebellar myoclonic syndromes.
    Lance JW.
    Adv Neurol; 1986 Feb; 43():33-55. PubMed ID: 3080851
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  • 15. Symptomatic myoclonus.
    Borg M.
    Neurophysiol Clin; 2006 Feb; 36(5-6):309-18. PubMed ID: 17336775
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  • 16. Spinocerebellar degeneration secondary to chronic intestinal malabsorption: a vitamin E deficiency syndrome.
    Harding AE, Muller DP, Thomas PK, Willison HJ.
    Ann Neurol; 1982 Nov; 12(5):419-24. PubMed ID: 7181449
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  • 18. Anti-ganglioside antibodies in coeliac disease with neurological disorders.
    Volta U, De Giorgio R, Granito A, Stanghellini V, Barbara G, Avoni P, Liguori R, Petrolini N, Fiorini E, Montagna P, Corinaldesi R, Bianchi FB.
    Dig Liver Dis; 2006 Mar; 38(3):183-7. PubMed ID: 16458087
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