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Journal Abstract Search

207 related items for PubMed ID: 1293984

  • 1. Classifications of hereditary ataxias. A critical overview.
    Campanella G, Filla A, De Michele G.
    Acta Neurol (Napoli); 1992; 14(4-6):408-19. PubMed ID: 1293984
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  • 2. [Hereditary ataxias].
    Tallaksen CM.
    Tidsskr Nor Laegeforen; 2008 Sep 11; 128(17):1977-80. PubMed ID: 18787576
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  • 4. A clinical classification of hereditary ataxias.
    Barbeau A, Sadibelouiz M, Sadibelouiz A, Roy M.
    Can J Neurol Sci; 1984 Nov 11; 11(4 Suppl):501-5. PubMed ID: 6509396
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  • 5. Familial Behr syndrome-like phenotype with autosomal dominant inheritance.
    Felicio AC, Godeiro-Junior C, Alberto LG, Pinto AP, Sallum JM, Teive HG, Barsottini OG.
    Parkinsonism Relat Disord; 2008 Nov 11; 14(4):370-2. PubMed ID: 17977780
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  • 9. [Siblings of early onset cerebellar ataxia with hypoalbuminemia].
    Hanihara T, Kubota H, Amano N, Iwamoto H, Iwabuchi K.
    Rinsho Shinkeigaku; 1995 Jan 11; 35(1):83-6. PubMed ID: 7781224
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  • 10. Parkinsonism & related disorders. Ataxias.
    Klockgether T.
    Parkinsonism Relat Disord; 2007 Jan 11; 13 Suppl 3():S391-4. PubMed ID: 18267270
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  • 11. Molecular genetics of hereditary ataxias.
    Banfi S, Zoghbi HY.
    Baillieres Clin Neurol; 1994 Aug 11; 3(2):281-95. PubMed ID: 7952848
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  • 12. [Classification and diagnosis of degenerative ataxias].
    Klockgether T, Bürk K, Auburger G, Dichgans J.
    Nervenarzt; 1995 Aug 11; 66(8):571-81. PubMed ID: 7566268
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  • 14. Peripheral nerve involvement in hereditary cerebellar and multisystem degenerative disorders.
    Berciano J, García A, Infante J.
    Handb Clin Neurol; 2013 Aug 11; 115():907-32. PubMed ID: 23931821
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  • 16. [Clinical identification of hereditary ataxias. A study of 38 cases in Colombia].
    Pedraza OL, Prieto JC, Casasbuenas OL, Espinosa E.
    Rev Neurol; 1997 Jul 11; 25(143):1016-22. PubMed ID: 9280625
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  • 17. Diagnosis and management of early- and late-onset cerebellar ataxia.
    Brusse E, Maat-Kievit JA, van Swieten JC.
    Clin Genet; 2007 Jan 11; 71(1):12-24. PubMed ID: 17204042
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  • 18. Mutations in SYNE1 lead to a newly discovered form of autosomal recessive cerebellar ataxia.
    Gros-Louis F, Dupré N, Dion P, Fox MA, Laurent S, Verreault S, Sanes JR, Bouchard JP, Rouleau GA.
    Nat Genet; 2007 Jan 11; 39(1):80-5. PubMed ID: 17159980
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  • 19. Primary degenerative cerebellar ataxias in ethnic Bengalees in West Bengal: some observations.
    Chakravarty A, Mukherjee SC.
    Neurol India; 2003 Jun 11; 51(2):227-34. PubMed ID: 14571010
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  • 20. Neurological approaches to the inherited ataxias.
    Refsum S, Skre H.
    Adv Neurol; 1978 Jun 11; 21():1-13. PubMed ID: 367114
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