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Journal Abstract Search

300 related items for PubMed ID: 4075075

  • 41. [Differential diagnosis of Friedreich ataxia].
    Claus D.
    Nervenarzt; 1989 Jan; 60(1):26-31. PubMed ID: 2922087
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  • 42. Electromyography and nerve conduction studies in Friedreich's ataxia and autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS).
    Bouchard JP, Barbeau A, Bouchard R, Bouchard RW.
    Can J Neurol Sci; 1979 May; 6(2):185-9. PubMed ID: 487308
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  • 44. Novel CAPN1 mutations extend the phenotypic heterogeneity in combined spastic paraplegia and ataxia.
    Lai LL, Chen YJ, Li YL, Lin XH, Wang MW, Dong EL, Wang N, Chen WJ, Lin X.
    Ann Clin Transl Neurol; 2020 Oct; 7(10):1862-1869. PubMed ID: 32860341
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  • 46. The global epidemiology of hereditary ataxia and spastic paraplegia: a systematic review of prevalence studies.
    Ruano L, Melo C, Silva MC, Coutinho P.
    Neuroepidemiology; 2014 Oct; 42(3):174-83. PubMed ID: 24603320
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  • 47. Early onset cerebellar ataxia with retained tendon reflexes: a clinical and genetic study of a disorder distinct from Friedreich's ataxia.
    Harding AE.
    J Neurol Neurosurg Psychiatry; 1981 Jun; 44(6):503-8. PubMed ID: 7276963
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  • 49. Evoked potential studies in Friedreich's ataxia and progressive early onset cerebellar ataxia.
    Vanasse M, Garcia-Larrea L, Neuschwander P, Trouillas P, Mauguière F.
    Can J Neurol Sci; 1988 Aug; 15(3):292-8. PubMed ID: 3208213
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  • 51. [Early auditory evoked potentials in spinocerebellar heredodegenerative involvement].
    Belkahia A, Ben H'mida M, Ben Jelloul N, Gassab A, Chakroun A.
    Ann Otolaryngol Chir Cervicofac; 1985 Aug; 102(2):97-103. PubMed ID: 4004026
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  • 52. An investigation of pyruvate metabolism in patients with cerebellar and spinocerebellar degeneration.
    Livingstone IR, Mastaglia FL, Pennington RJ.
    J Neurol Sci; 1980 Oct; 48(1):123-32. PubMed ID: 6893466
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  • 55. Early-onset cerebellar ataxia with retained tendon reflexes.
    Ozeren A, Araç N, Ulkü A.
    Acta Neurol Scand; 1989 Dec; 80(6):593-7. PubMed ID: 2618587
    [Abstract] [Full Text] [Related]

  • 56. A linkage study of hereditary ataxias and related disorders. Evidence of heterogeneity of dominant cerebellar ataxia.
    Pedersen L, Platz P, Ryder LP, Lamm LU, Dissing J.
    Hum Genet; 1980 Dec; 54(3):371-83. PubMed ID: 6772543
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  • 57. [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
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