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Journal Abstract Search

124 related items for PubMed ID: 3463881

  • 1. Familial ataxia with extreme difference in age of clinical onset.
    Amit R, Granit G, Shapira Y.
    Neuropediatrics; 1986 Aug; 17(3):165-7. PubMed ID: 3463881
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  • 3. Brainstem auditory evoked responses in hereditary spinocerebellar ataxias.
    Knezevic W, Stewart-Wynne EG.
    Clin Exp Neurol; 1985 Aug; 21():149-55. PubMed ID: 3870433
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  • 5. Spinocerebellar ataxia type 2 (SCA 2) in an infant with extreme CAG repeat expansion.
    Babovic-Vuksanovic D, Snow K, Patterson MC, Michels VV.
    Am J Med Genet; 1998 Oct 12; 79(5):383-7. PubMed ID: 9779806
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  • 6. Hereditary ataxia.
    Rosenberg RN, Grossman A.
    Neurol Clin; 1989 Feb 12; 7(1):25-36. PubMed ID: 2564162
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  • 7. [Some problems on the clinical phenotype of Machado-Joseph disease in relation between their ages at onset].
    Iwabuchi K, Kogure T, Oda T, Kato Y, Ohtani K, Endo K, Kosaka K, Amano N, Yagishita S.
    No To Shinkei; 1993 Mar 12; 45(3):246-54. PubMed ID: 8323819
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  • 9. Machado-Joseph disease: an autosomal dominant motor system degeneration.
    Rosenberg RN.
    Mov Disord; 1992 Mar 12; 7(3):193-203. PubMed ID: 1620135
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  • 11. Cerebellar and brainstem hypometabolism in olivopontocerebellar atrophy detected with positron emission tomography.
    Gilman S, Markel DS, Koeppe RA, Junck L, Kluin KJ, Gebarski SS, Hichwa RD.
    Ann Neurol; 1988 Mar 12; 23(3):223-30. PubMed ID: 3259853
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  • 12. Brain choline acetyltransferase reduction in dominantly inherited olivopontocerebellar atrophy.
    Kish SJ, Currier RD, Schut L, Perry TL, Morito CL.
    Ann Neurol; 1987 Aug 12; 22(2):272-5. PubMed ID: 3477997
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  • 15. [Neuropathological study of autosomal dominant ataxia linked to loci on chromosome 6p (SCA 1)].
    Hamada K, Fukazawa T, Yanagihara T, Hamada T, Yoshida K, Sasaki H, Tashiro K.
    No To Shinkei; 1993 Nov 12; 45(11):1045-9. PubMed ID: 8297664
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  • 16. Primary degeneration of the granular layer of the cerebellum. A study of 14 patients and review of the literature.
    Pascual-Castroviejo I, Gutierrez M, Morales C, Gonzalez-Mediero I, Martínez-Bermejo A, Pascual-Pascual SI.
    Neuropediatrics; 1994 Aug 12; 25(4):183-90. PubMed ID: 7824090
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  • 17. Brain acetylcholinesterase activity is markedly reduced in dominantly-inherited olivopontocerebellar atrophy.
    Kish SJ, Schut L, Simmons J, Gilbert J, Chang LJ, Rebbetoy M.
    J Neurol Neurosurg Psychiatry; 1988 Apr 12; 51(4):544-8. PubMed ID: 3164041
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  • 19. [A clinical study of a family affected with HLA-linked hereditary spinocerebellar ataxia].
    Sasaki H, Hamada T, Wakisaka A, Tashiro K.
    No To Shinkei; 1990 Nov 12; 42(11):1103-11. PubMed ID: 2076357
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