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Journal Abstract Search

292 related items for PubMed ID: 973068

  • 1. [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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  • 2. [Ramsay-Hunt's syndrome: a case report with pathological examination (author's transl)].
    Choteau P, Gray F, Warot P, Dereux JF.
    Rev Neurol (Paris); 1980 Feb; 136(12):837-52. PubMed ID: 7291843
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  • 3. [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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  • 4. Ramsay Hunt syndrome: progressive mental deterioration in association with unusual cerebral white matter change.
    Kobayashi K, Morikawa K, Fukutani Y, Miyazu K, Nakamura I, Yamaguchi N, Watanabe H.
    Clin Neuropathol; 1994 Feb; 13(2):88-96. PubMed ID: 8205732
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  • 5. [Myoclonic cerebellar dyssynergia (Ramsay Hunt). Description of 2 cases].
    Fryze C, Korwin-Piotrowska T, Potemkowski A, Niezabitowski K.
    Neurol Neurochir Pol; 1985 Feb; 19(6):508-11. PubMed ID: 3835491
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  • 6. [Progressive myoclonic epilepsy: anatomo - clinical study of a sporadic case with a marked cerebellar symptomatology (author's transl)].
    Nardelli E, Buonanno F, Onnis L, Rizzuto N.
    Riv Patol Nerv Ment; 1975 Feb; 96(4):221-32. PubMed ID: 1232666
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  • 10. [The clinical picture of olivo-ponto-cerebellar atrophy (Déjérine-Thomas)].
    Kulawik H, Roitzsch E, Barz H.
    Psychiatr Neurol Med Psychol (Leipz); 1972 Mar; 24(3):119-27. PubMed ID: 5034933
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  • 14. Menzel's hereditary ataxia with slow eye movements and myoclonus. A clinico-pathological study.
    Rondot P, De Recondo J, Davous P, Vedrenne C.
    J Neurol Sci; 1983 Sep; 61(1):65-80. PubMed ID: 6631453
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  • 18. [Clinical features of the Shy-Drager syndrome--comparison with olivo-ponto-cerebellar atrophy and striato-nigral degeneration].
    Hirayama K, Kita K.
    No To Shinkei; 1985 Jul; 37(7):637-45. PubMed ID: 3904781
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