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Journal Abstract Search

188 related items for PubMed ID: 632821

  • 1. Progressive myoclonus and epilepsy with dentatorubral degeneration: a clinicopathological study of the Ramsay Hunt syndrome.
    Bird TD, Shaw CM.
    J Neurol Neurosurg Psychiatry; 1978 Feb; 41(2):140-9. PubMed ID: 632821
    [Abstract] [Full Text] [Related]

  • 2. Ramsay Hunt syndrome in dentatorubral-pallidoluysian atrophy.
    Suzuki S, Kamoshita S, Ninomura S.
    Pediatr Neurol; 1985 Feb; 1(5):298-301. PubMed ID: 3880416
    [Abstract] [Full Text] [Related]

  • 3. [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
    [Abstract] [Full Text] [Related]

  • 4. [Neuropathological study of a case of progressive familial myoclonic epilepsy (author's transl)].
    Ferro FM, Mazza S, D'Angelo C.
    Riv Patol Nerv Ment; 1975 Feb; 96(2):127-34. PubMed ID: 1228876
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. [Dentatorubropallidoluysian atrophy (DRPLA): comparative pathological study on clinical groups classified into juvenile, early adult and late adult types].
    Takeda S, Takahashi H, Ikuta F.
    No To Shinkei; 1992 Feb; 44(2):111-6. PubMed ID: 1567729
    [Abstract] [Full Text] [Related]

  • 7. Hereditary dentatorubral-pallidoluysian atrophy.
    Oyanagi S.
    Neuropathology; 2000 Sep; 20 Suppl():S42-6. PubMed ID: 11037186
    [Abstract] [Full Text] [Related]

  • 8. [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 Sep; 96(4):221-32. PubMed ID: 1232666
    [Abstract] [Full Text] [Related]

  • 9. [(Neurological CPC.55). A 60-year-old woman with progressive cerebellar ataxia, myoclonus, and dementia].
    Morikawa N, Mori H, Sumino S, Kodera M, Shirai T, Kondo T, Mizuno Y.
    No To Shinkei; 1997 Jul; 49(7):663-71. PubMed ID: 9234257
    [Abstract] [Full Text] [Related]

  • 10. [Hereditary dentatorubropallidoluysian atrophy--clinical variants in a family and degeneration of cerebral white matter in a proband].
    Miyashita K, Inuzuka T, Ishikawa A, Kondo H, Kawakami A, Takeda S, Ikuta F, Yuasa T.
    No To Shinkei; 1992 Mar; 44(3):279-84. PubMed ID: 1591106
    [Abstract] [Full Text] [Related]

  • 11. Action myoclonus, Ramsay Hunt syndrome, and other cerebellar myoclonic syndromes.
    Lance JW.
    Adv Neurol; 1986 Mar; 43():33-55. PubMed ID: 3080851
    [Abstract] [Full Text] [Related]

  • 12. [Progressive myoclonus epilepsy of Unverricht-Lundborg. Anatomo-clinical study of an abiotrophic form].
    Franck G, Reznik M.
    Acta Neurol Psychiatr Belg; 1967 Sep; 67(9):713-30. PubMed ID: 4965315
    [No Abstract] [Full Text] [Related]

  • 13. 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
    [Abstract] [Full Text] [Related]

  • 14. Myoclonic epilepsia partialis continua and Friedreich Ataxia.
    Ziegler DK, Van Speybroech NW, Seitz EF.
    Arch Neurol; 1974 Nov; 31(5):308-11. PubMed ID: 4414767
    [No Abstract] [Full Text] [Related]

  • 15. Dentatorubral-pallidoluysian atrophy: clinical features are closely related to unstable expansions of trinucleotide (CAG) repeat.
    Ikeuchi T, Koide R, Tanaka H, Onodera O, Igarashi S, Takahashi H, Kondo R, Ishikawa A, Tomoda A, Miike T.
    Ann Neurol; 1995 Jun; 37(6):769-75. PubMed ID: 7778850
    [Abstract] [Full Text] [Related]

  • 16. Ramsay Hunt syndrome: New impressions in the era of molecular genetics.
    Teive HAG, Cassou E, Coutinho L, Camargo CHF, Munhoz RP.
    Parkinsonism Relat Disord; 2022 Apr; 97():101-104. PubMed ID: 35430109
    [Abstract] [Full Text] [Related]

  • 17. [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 Apr; 142(1):29-33. PubMed ID: 3085192
    [Abstract] [Full Text] [Related]

  • 18. [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 Apr; 136(12):837-52. PubMed ID: 7291843
    [Abstract] [Full Text] [Related]

  • 19. Progressive myoclonus epilepsy with focal brainstem degeneration and paternal inheritance. An autopsy report of 4 cases from 2 pedigrees.
    Moss TH, Stevens DL, Campbell MJ.
    Clin Neuropathol; 1996 Apr; 15(2):106-12. PubMed ID: 8925594
    [Abstract] [Full Text] [Related]

  • 20. Progressive supranuclear palsy with action myoclonus, seizures.
    Kurihara T, Landau WM, Torack RM.
    Neurology; 1974 Mar; 24(3):219-23. PubMed ID: 4855949
    [No Abstract] [Full Text] [Related]

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