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PUBMED FOR HANDHELDS

Journal Abstract Search


207 related items for PubMed ID: 5652992

  • 1. Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. II. Neurologic, genetic, and electrophysiologic findings in various neuronal degenerations.
    Dyck PJ, Lambert EH.
    Arch Neurol; 1968 Jun; 18(6):619-25. PubMed ID: 5652992
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  • 2. Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies.
    Dyck PJ, Lambert EH.
    Arch Neurol; 1968 Jun; 18(6):603-18. PubMed ID: 4297451
    [No Abstract] [Full Text] [Related]

  • 3. Sensory potentials in polyneuropathy.
    Buchthal F, Rosenfalck A.
    Brain; 1971 Jun; 94(2):241-62. PubMed ID: 5571042
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  • 5. An electrophysiological and pathological study of peripheral nerves in Friedreich's ataxia.
    McLeod JG.
    J Neurol Sci; 1971 Mar; 12(3):333-49. PubMed ID: 5550263
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  • 6. [Electrophysiologic studies of patients with neural muscular atrophy].
    Thielemann B, Müller D, von Specht H, Koch RD.
    Psychiatr Neurol Med Psychol (Leipz); 1987 Apr; 39(4):202-8. PubMed ID: 3474672
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  • 12. [Investigations of peripheral and central somatosensory pathways in peroneal muscular atrophy and Friedreich's heredoataxia (author's transl)].
    Sauer M.
    Arch Psychiatr Nervenkr (1970); 1980 Apr; 228(3):223-42. PubMed ID: 7416937
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  • 15. Variable sensory nerve conduction parameters in late onset Friedreich ataxia.
    Alix JJ, Alam T, Garrard K, Martindale J, Shanmugarajah P, Ganesh Rao D, Hadjivassiliou M.
    Muscle Nerve; 2017 Feb; 55(2):E7-E8. PubMed ID: 27491039
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  • 16. [Evaluation of the conductive velocity of individual motor nerve fibre bundles. A neurophysiological study].
    Drechsler B.
    Dtsch Z Nervenheilkd; 1969 Feb; 195(1):19-25. PubMed ID: 4308447
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  • 20. Hereditary distal spinal muscular atrophy. A report on 34 cases and a review of the literature.
    Harding AE, Thomas PK.
    J Neurol Sci; 1980 Mar; 45(2-3):337-48. PubMed ID: 7365507
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