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Journal Abstract Search

221 related items for PubMed ID: 7172528

  • 1. [Progressive supranuclear palsy with familial occurrence of spinocerebellar degeneration].
    Yamamura Y, Kito S, Itoga E, Kajiwara H.
    Rinsho Shinkeigaku; 1982 Jul; 22(7):586-93. PubMed ID: 7172528
    [No Abstract] [Full Text] [Related]

  • 2. Autosomal recessive spino-olivo-cerebellar degeneration without ataxia.
    Staal A, Stefanko SZ, Jennekens FG, Vries-Bos LH, van Gijn J.
    J Neurol Neurosurg Psychiatry; 1983 Jul; 46(7):648-52. PubMed ID: 6886703
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  • 3. 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]

  • 4. [Hereditary degenerative spinocerebellar diseases in Tunisia with manometric studies in bladder disorders (author's transl)].
    Ben Hamida M, Madani S, Zmerli S, Chami I, Annabi A, Jamoussi M, Marzouki M, Rachdi M, Samoud S, Talbi M.
    Rev Neurol (Paris); 1980 Feb; 136(8-9):495-508. PubMed ID: 7221327
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  • 5. [Epilepsy and hereditary spino-cerebellar degeneration].
    Gayral L, Gayral J.
    J Genet Hum; 1969 May; 17(1):127-36. PubMed ID: 4980118
    [No Abstract] [Full Text] [Related]

  • 6. [Genetic aspects of some spino-cerebellar degenerations].
    Badiu G.
    Stud Cercet Neurol; 1969 May; 14(5):311-24. PubMed ID: 4906012
    [No Abstract] [Full Text] [Related]

  • 7. [2 autopsy cases of the spinocerebellar degeneration with cerebral atrophy].
    Kato Y, Takayama K, Tsujiyama Y, Kaga T, Satowa H.
    No To Shinkei; 1970 Oct; 22(10):1201-8. PubMed ID: 5536190
    [No Abstract] [Full Text] [Related]

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  • 10. [Insulin availability in some familial inherited neurological syndromes (author's transl)].
    Fratino P, Kauchtschischvili G, Nappi G, Poloni M, Favino A, Criffò A.
    Riv Patol Nerv Ment; 1974 Oct; 95(5):624-31. PubMed ID: 4283420
    [No Abstract] [Full Text] [Related]

  • 11. [2 families in the Himeji area with spinocerebellar degeneration with primary symptoms of divergence paralysis].
    Itoga E, Kito S, Yamamoto M, Uchida Y.
    Rinsho Shinkeigaku; 1975 Apr; 15(4):212-7. PubMed ID: 1170060
    [No Abstract] [Full Text] [Related]

  • 12. A case of familial spinocerebellar degeneration with hypobetalipoproteinemia.
    Korula J, Namasivayam RK, Shadangi TN, Reddy PK, Raman PT.
    Neurol India; 1976 Mar; 24(1):41-5. PubMed ID: 179026
    [No Abstract] [Full Text] [Related]

  • 13. [Electroretinography and electroencephalography in spinocerebellar degenerations].
    Stanescu B, Wawernia E.
    Arch Ophtalmol Rev Gen Ophtalmol; 1973 Jan; 33(1):43-8. PubMed ID: 4267723
    [No Abstract] [Full Text] [Related]

  • 14. [Progressive nuclear ophthalmoplegia and hereditary spinal cerebellar degeneration. Study of 1 anatomo-clinical case].
    Brion S, De Recondo J.
    Rev Neurol (Paris); 1967 May; 116(5):383-400. PubMed ID: 6052813
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  • 16. Spinocerebellar degeneration with divergence paralysis as the earliest sign.
    Itoga E.
    Hiroshima J Med Sci; 1980 Dec; 29(4):155-61. PubMed ID: 7204104
    [No Abstract] [Full Text] [Related]

  • 17. [A clinical study of spinocerebellar degeneration and its genetic background on Guam (author's transl)].
    Murakami N, Chen KM, Gajdusek DC, Sobue I.
    Rinsho Shinkeigaku; 1980 Apr; 20(4):271-9. PubMed ID: 7408331
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  • 20. [Spinocerebellar degeneration with slow eye movement--with special reference to neuropathological background of disturbance of ocular movement].
    Mizutani T.
    Rinsho Shinkeigaku; 1986 Feb; 26(2):166-74. PubMed ID: 3698420
    [No Abstract] [Full Text] [Related]

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