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Journal Abstract Search

150 related items for PubMed ID: 4763007

  • 1. [Familial atrophic form of spinocerebellar ataxia].
    Gaj T, Grendus-Tota B.
    Neurol Neurochir Pol; 1973; 7(5):679-83. PubMed ID: 4763007
    [No Abstract] [Full Text] [Related]

  • 2. [Amyotrophic form of a spinocerebellar degeneration. Anatomoclinical study and nosological discussion].
    Boudouresques J, Toga M, Khalil R, Gosset A, Vigouroux RA, Pellissier JF.
    Rev Neurol (Paris); 1971 Jul; 125(1):25-38. PubMed ID: 5138162
    [No Abstract] [Full Text] [Related]

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  • 5. Autosomal recessive cerebellar ataxias.
    Palau F, Espinós C.
    Orphanet J Rare Dis; 2006 Nov 17; 1():47. PubMed ID: 17112370
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  • 6. [Ataxia myatrophica].
    Wieczorkiewicz MA, Zdzienicka E.
    Neurol Neurochir Pol; 1972 Nov 17; 6(3):387-91. PubMed ID: 5032289
    [No Abstract] [Full Text] [Related]

  • 7. [Autosomal recessive cerebellar ataxias].
    Tranchant C, Anheim M.
    Presse Med; 2009 Dec 17; 38(12):1852-9. PubMed ID: 19442480
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  • 8. Clinical and electrodiagnostic features of Charcot-Marie-Tooth syndrome.
    Brust JC, Lovelace RE, Devi S.
    Acta Neurol Scand Suppl; 1978 Dec 17; 68():1-142. PubMed ID: 212921
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  • 10. Hereditary spastic ataxia: report of a family through four generations.
    Ishino H, Sato M, Terao A, Hayahara T, Otsuki S.
    Folia Psychiatr Neurol Jpn; 1971 Dec 17; 25(4):269-81. PubMed ID: 5172645
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  • 11. Cranial computerized tomography in spinocerebellar atrophies.
    Claus D, Aschoff JC.
    Ann N Y Acad Sci; 1981 Dec 17; 374():831-8. PubMed ID: 6951461
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  • 13. [Clinical and genetic analysis of 188 families with spinocerebellar degeneration. Friedreich's disease and P. Marie's hereditary ataxias].
    Ben Hamida M, Attia-Romdhane N, Triki CH, Oueslati S, Hentati F.
    Rev Neurol (Paris); 1991 Dec 17; 147(12):798-808. PubMed ID: 1780608
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  • 16. [Progressive nuclear ophthalmoplegia and hereditary spinal cerebellar degeneration. Study of 1 anatomo-clinical case].
    Brion S, De Recondo J.
    Rev Neurol (Paris); 1967 May 17; 116(5):383-400. PubMed ID: 6052813
    [No Abstract] [Full Text] [Related]

  • 17. Heredoataxia (spinocerebellar degeneration), ERG alterations, temporal aspects.
    Stanescu-Segal B, Michiels J.
    Ophthalmologica; 1979 May 17; 178(5):267-72. PubMed ID: 492674
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  • 19. Dominant spino-pontine atrophy. Report of a family through three generations.
    Taniguchi R, Konigsmark BW.
    Brain; 1971 May 17; 94(2):349-58. PubMed ID: 5571046
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