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PUBMED FOR HANDHELDS

Journal Abstract Search


116 related items for PubMed ID: 5621303

  • 21. [Stylohyoid apparatus and malformations of the occipito-vertebral joint. Apropos of 5 cases].
    Arnould G, Tridon P, Lazenaire M, Picard L, Weber M, Masingue M.
    Rev Otoneuroophtalmol; 1969; 41(4):190-5. PubMed ID: 5387233
    [No Abstract] [Full Text] [Related]

  • 22. [Early symptoms of cerebellar atrophy in chronic alcoholics (author's transl)].
    Avdaloff W, Mauersberger W.
    Nervenarzt; 1981 Jun; 52(6):333-9. PubMed ID: 7266696
    [No Abstract] [Full Text] [Related]

  • 23. [Cerebral calcinosis (Fahr's disease). Clinical and radiologic aspects].
    Macchi L, Vercesi G.
    Minerva Radiol; 1968 May; 13(5):231-46. PubMed ID: 5309786
    [No Abstract] [Full Text] [Related]

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  • 25. [Clinical characteristics of various motor disorders in diencephalitis].
    Shmidt ZN.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1968 May; 67(8):1143-8. PubMed ID: 5680521
    [No Abstract] [Full Text] [Related]

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  • 27. Familial cerebellar atrophy.
    Sullivan JA, McConnell JR, Woody RC.
    J Ark Med Soc; 1985 Mar; 81(10):497-9. PubMed ID: 3157669
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  • 29. [Late cerebellar atrophy with osteo-tendinous areflexia and progressive ophthalmoplegia with dominant autosomal heredity. Long-term study in 6 generations of one family].
    Bravaccio F, Del Vecchio M, Paolozzi C, Ghetti B, Tripaldelli B, Amati A, Guazzi GC.
    Acta Neurol (Napoli); 1971 Mar; 26(3):361-74. PubMed ID: 5094472
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  • 31. Dysarthria--clumsy hand syndrome and cerebellar hemorrhage.
    Roy EP, Keefover RW, Riggs JE, Marano GD.
    Ann Neurol; 1987 Apr; 21(4):415-6. PubMed ID: 3579229
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  • 34. Hereditary cerebellar cortical abiotrophy in the Gordon Setter.
    de Lahunta A, Fenner WR, Indrieri RJ, Mellick PW, Gardner S, Bell JS.
    J Am Vet Med Assoc; 1980 Sep 15; 177(6):538-41. PubMed ID: 7440348
    [No Abstract] [Full Text] [Related]

  • 35. [Progressive nuclear ophthalmoplegia and hereditary spinal cerebellar degeneration. Study of 1 anatomo-clinical case].
    Brion S, De Recondo J.
    Rev Neurol (Paris); 1967 May 15; 116(5):383-400. PubMed ID: 6052813
    [No Abstract] [Full Text] [Related]

  • 36. Infantile onset progressive cerebellar atrophy and anterior horn cell degeneration: a late onset variant of PCH-1?
    Castro-Gago M, Gómez-Lado C, Eirís-Puñal J.
    Eur J Paediatr Neurol; 2009 Sep 15; 13(5):473; author reply 474. PubMed ID: 18929497
    [No Abstract] [Full Text] [Related]

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  • 38. Dominant olivopontocerebellar degeneration and optic pathway atrophy: a family report.
    Triau E, Dom R, Ververken D, Carton H.
    Clin Neuropathol; 1982 Sep 15; 1(2):67-72. PubMed ID: 7168919
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