These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

237 related items for PubMed ID: 1232666

  • 1. [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; 96(4):221-32. PubMed ID: 1232666
    [Abstract] [Full Text] [Related]

  • 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; 136(12):837-52. PubMed ID: 7291843
    [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. [Spinocerebellar degeneration, optic atrophy, epilepsy, myoclonus and mitochondrial myopathy: a case report (author's transl)].
    Roger J, Pellissier JF, Dravet C, Bureau-Paillas M, Arnoux M, Larrieu JL.
    Rev Neurol (Paris); 1982 Feb; 138(3):187-200. PubMed ID: 6810437
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. FAME 3: a novel form of progressive myoclonus and epilepsy.
    Carr JA, van der Walt PE, Nakayama J, Fu YH, Corfield V, Brink P, Ptacek L.
    Neurology; 2007 Apr 24; 68(17):1382-9. PubMed ID: 17452583
    [Abstract] [Full Text] [Related]

  • 8. [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 Apr 24; 96(2):127-34. PubMed ID: 1228876
    [Abstract] [Full Text] [Related]

  • 9. [The basic hereditary myoclonus-epilepsy-dementia syndromes. Progressive myoclonus epilepsies--myoclonic cerebellar dyssynergia--myoclonic variants of the 3 postinfantile types of amaurotic idiocy].
    Diebold K.
    Monogr Gesamtgeb Psychiatr Psychiatry Ser; 1973 Apr 24; 8():1-254. PubMed ID: 4269086
    [No Abstract] [Full Text] [Related]

  • 10. [Progressive myoclonus epilepsy in two siblings and 5 cases with dyssynergia cerebellaris myoclonica in several generations of a kinship, a clinical and genetic study].
    Diebold K, Kastner M, Penin H.
    Nervenarzt; 1974 Nov 24; 45(11):595-601. PubMed ID: 4217888
    [No Abstract] [Full Text] [Related]

  • 11. [An autopsied case of idiopathic late cortical cerebellar atrophy--comparison with other cortical cerebellar atrophy].
    Iwabuchi K, Yagishita S.
    Rinsho Shinkeigaku; 1990 Nov 24; 30(11):1190-6. PubMed ID: 2085923
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. [The role of mitochondrial encephalopathies in progressive myoclonus epilepsy].
    Roger J, Bureau M, Dravet C, Genton P, Tassinari CA, Michelucci R.
    Rev Neurol (Paris); 1991 Nov 24; 147(6-7):480-90. PubMed ID: 1962055
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. [Striatonigral degeneration associated with olivopontocerebellar atrophy. Anatomo-clinical study of 3 cases. Nosologic discussion].
    Gosset A, Pellissier JF, Delpuech F, Khalil R.
    Rev Neurol (Paris); 1983 Nov 24; 139(2):125-39. PubMed ID: 6410487
    [Abstract] [Full Text] [Related]

  • 17. [Progressive supranuclear palsy: description of a case of early occurrence associated with muscular atrophies (author's transl)].
    Barontini F, Cappelli L, Marconi G.
    Riv Patol Nerv Ment; 1978 Nov 24; 99(4):195-206. PubMed ID: 752181
    [Abstract] [Full Text] [Related]

  • 18. [Diphenylhydantoin, epilepsy, cerebellar atrophy--histological and electron microscope examinations (author's transl)].
    Breiden-Arends C, Gullotta F.
    Fortschr Neurol Psychiatr; 1981 Nov 24; 49(11):406-14. PubMed ID: 7343457
    [Abstract] [Full Text] [Related]

  • 19. [(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 24; 49(7):663-71. PubMed ID: 9234257
    [Abstract] [Full Text] [Related]

  • 20. [On the differential diagnosis of progressive myoclonic epilepsy].
    Diebold K.
    Fortschr Neurol Psychiatr Grenzgeb; 1968 Oct 24; 36(10):545-75. PubMed ID: 4974222
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 12.