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Journal Abstract Search

137 related items for PubMed ID: 3098158

  • 21. Action myoclonus, Ramsay Hunt syndrome, and other cerebellar myoclonic syndromes.
    Lance JW.
    Adv Neurol; 1986; 43():33-55. PubMed ID: 3080851
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  • 22. Hereditary spino-cerebellar degeneration and Ramsay-Hunt disease.
    Penneau D, Bigorgne JC, Fressinaud-Masdefeix L.
    Cah Med; 1974 Feb; 15(2):93-6. PubMed ID: 4848865
    [No Abstract] [Full Text] [Related]

  • 23. A clinical analysis of myoclonus epilepsy (Unverricht-Lundborg), myoclonic cerebellar dyssynergy (Hunt) and hepatolenticular degeneration (Wilson).
    WOHLFART G, HOOK O.
    Acta Psychiatr Neurol Scand; 1951 Feb; 26(2):219-45. PubMed ID: 14902532
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  • 26. MELAS, myoclonus, ataxia and deficiencies of complexes I and IV in muscle mitochondria.
    Yamanaka R, Nomura Y, Segawa M, Nonaka I.
    Acta Paediatr Jpn; 1987 Oct; 29(5):761-7. PubMed ID: 2849285
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  • 27. Progressive myoclonus epilepsies. Criteria for diagnosis on the basis of the follow-up of 37 cases.
    Guazzi GC, Federico A.
    Acta Neurol (Napoli); 1992 Oct; 14(4-6):469-84. PubMed ID: 1293989
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  • 28. MERRF: a model disease for understanding the principles of mitochondrial genetics.
    Shoffner JM, Lott MT, Wallace DC.
    Rev Neurol (Paris); 1991 Oct; 147(6-7):431-5. PubMed ID: 1962048
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  • 29. Mitochondrial encephalomyopathies: a correlation between neuropathological findings and defects in mitochondrial DNA.
    McKelvie PA, Morley JB, Byrne E, Marzuki S.
    J Neurol Sci; 1991 Mar; 102(1):51-60. PubMed ID: 1906931
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  • 30. [Action myoclonus in Ramsay Hunt myoclonic cerebellar dyssynergyand in Lance-Adams syndrome].
    Tassinari CA, Roger J, Regis H, Sedan R, Lyagoubi S, Gambarelli F, Vallicioni P, Dravet C, Soulayrol R.
    Rev Neurol (Paris); 1970 Nov; 123(5):335-6. PubMed ID: 5513635
    [No Abstract] [Full Text] [Related]

  • 31. [An autopsy case of myoclonus epilepsy associated with ragged-red fibers (Fukuhara disease)].
    Takeda S, Wakabayashi K, Ohama E, Ikuta F, Homma Y, Fukuhara N, Tanaka K, Yoneda M, Miyatake T.
    No To Shinkei; 1987 Dec; 39(12):1171-9. PubMed ID: 3128314
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  • 34. [Familial cases of mitochondrial cytopathy].
    Ishitsu T, Matsuda I, Kitano A, Shimoji A, Kimura H.
    Rinsho Shinkeigaku; 1987 Aug; 27(8):983-9. PubMed ID: 3121229
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  • 37. [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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