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Journal Abstract Search

171 related items for PubMed ID: 7231446

  • 1. Peripheral neuropathy in spinocerebellar degenerations.
    McLeod JG, Evans WA.
    Muscle Nerve; 1981; 4(1):51-61. PubMed ID: 7231446
    [Abstract] [Full Text] [Related]

  • 2. [Clinical and electrophysiological findings in various hereditary sensory neuropathies].
    Caruso G, Santoro L, Perretti A.
    Acta Neurol (Napoli); 1992; 14(4-6):345-62. PubMed ID: 1293978
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  • 3. Electrophysiological and pathological studies in spinocerebellar degenerations.
    McLeod JG, Morgan JA.
    Proc Aust Assoc Neurol; 1976; 13():113-7. PubMed ID: 1028997
    [Abstract] [Full Text] [Related]

  • 4. Motor evoked potentials by magnetic stimulation in hereditary and sporadic ataxia.
    Mondelli M, Rossi A, Scarpini C, Guazzi GC.
    Electromyogr Clin Neurophysiol; 1995 Nov; 35(7):415-24. PubMed ID: 8549432
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  • 5. The INFIR Cohort Study: assessment of sensory and motor neuropathy in leprosy at baseline.
    Van Brakel WH, Nicholls PG, Das L, Barkataki P, Maddali P, Lockwood DN, Wilder-Smith E.
    Lepr Rev; 2005 Dec; 76(4):277-95. PubMed ID: 16411508
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  • 6. Sensory neuropathy in infantile onset spinocerebellar ataxia (IOSCA).
    Koskinen T, Sainio K, Rapola J, Pihko H, Paetau A.
    Muscle Nerve; 1994 May; 17(5):509-15. PubMed ID: 8159181
    [Abstract] [Full Text] [Related]

  • 7. Nerve conduction study, electromyography and somatosensory evoked potentials in non-Friedreich early onset cerebellar ataxia. A comparative study with Friedreich's ataxia and late onset cerebellar ataxia.
    Mondelli M, Decchi B, Parlanti S, Scarpini C, Rossi A.
    Electromyogr Clin Neurophysiol; 1992 May; 32(4-5):207-14. PubMed ID: 1600884
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  • 9. Nerve conduction study of ulnar nerve in volleyball players.
    Ozbek A, Bamaç B, Budak F, Yenigün N, Colak T.
    Scand J Med Sci Sports; 2006 Jun; 16(3):197-200. PubMed ID: 16643198
    [Abstract] [Full Text] [Related]

  • 10. [Clinical, multimodal electrophysiological study of a family with progressive cerebellar ataxia and late deafness and an autosomal recessive inheritance].
    Ragno M, Curatola L, Rossi R, Salvolini U.
    Acta Neurol (Napoli); 1992 Jun; 14(4-6):431-9. PubMed ID: 1293986
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  • 13. [A family of X-linked motor and sensory neuropathy with a new type of connexin32 mutation].
    Ohnishi A, Yoshimura T, Takazawa A, Hashimoto T, Yamamoto T, Fukushima Y.
    Rinsho Shinkeigaku; 1995 Aug; 35(8):843-9. PubMed ID: 8665724
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  • 15. Autosomal dominant cerebellar ataxia: phenotypic differences in genetically defined subtypes?
    Schöls L, Amoiridis G, Büttner T, Przuntek H, Epplen JT, Riess O.
    Ann Neurol; 1997 Dec; 42(6):924-32. PubMed ID: 9403486
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  • 16. Peripheral neuropathy associated with mitochondrial myopathy.
    Yiannikas C, McLeod JG, Pollard JD, Baverstock J.
    Ann Neurol; 1986 Aug; 20(2):249-57. PubMed ID: 3019229
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  • 19. 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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