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Journal Abstract Search

162 related items for PubMed ID: 7964809

  • 1. Peroneal muscular atrophy with pyramidal tract features (hereditary motor and sensory neuropathy type V): a clinical, neurophysiological, and pathological study of a large kindred.
    Frith JA, McLeod JG, Nicholson GA, Yang F.
    J Neurol Neurosurg Psychiatry; 1994 Nov; 57(11):1343-6. PubMed ID: 7964809
    [Abstract] [Full Text] [Related]

  • 2. Peroneal muscular atrophy with pyramidal features.
    Harding AE, Thomas PK.
    J Neurol Neurosurg Psychiatry; 1984 Feb; 47(2):168-72. PubMed ID: 6707656
    [Abstract] [Full Text] [Related]

  • 3. The clinical features of hereditary motor and sensory neuropathy types I and II.
    Harding AE, Thomas PK.
    Brain; 1980 Jun; 103(2):259-80. PubMed ID: 7397478
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  • 4. Motor nerve conduction velocity in peroneal muscular atrophy: evidence for genetic heterogeneity.
    Thomas PK, Calne DB.
    J Neurol Neurosurg Psychiatry; 1974 Jan; 37(1):68-75. PubMed ID: 4813428
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  • 7. Hereditary motor and sensory polyneuropathy (peroneal muscular atrophy).
    Thomas PK, Calne DB, Stewart G.
    Ann Hum Genet; 1974 Oct; 38(2):111-53. PubMed ID: 4467779
    [No Abstract] [Full Text] [Related]

  • 8. Peroneal muscular atrophy. Part 1. Clinical and electrophysiological study.
    Bouché P, Gherardi R, Cathala HP, Lhermitte F, Castaigne P.
    J Neurol Sci; 1983 Oct; 61(3):389-99. PubMed ID: 6317809
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  • 9. Hereditary motor and sensory neuropathy. Clinical, genetic and electrodiagnostic studies.
    Vasilescu C.
    Rom J Neurol Psychiatry; 1993 Oct; 31(3-4):207-19. PubMed ID: 8011484
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  • 10. Peroneal muscular atrophy with autosomal dominant inheritance.
    McLeod JG, Low PA.
    Clin Exp Neurol; 1977 Oct; 14():142-53. PubMed ID: 616594
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  • 11. Muscle-nerve involvement in autosomal dominant progressive external ophthalmoplegia with hypogonadism.
    Melberg A, Lundberg PO, Henriksson KG, Olsson Y, Stålberg E.
    Muscle Nerve; 1996 Jun; 19(6):751-7. PubMed ID: 8609926
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  • 12. Peripheral neurofibromatosis and peroneal muscular atrophy.
    Bosch EP, Murphy MJ, Cancilla PA.
    Neurology; 1981 Nov; 31(11):1408-14. PubMed ID: 6796901
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  • 14. Recurrent Guillain Barre' syndrome.
    Das A, Kalita J, Misra UK.
    Electromyogr Clin Neurophysiol; 2004 Mar; 44(2):95-102. PubMed ID: 15061403
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  • 17. Nerve conduction studies in spastic paraplegia, optic atrophy, and neuropathy (SPOAN) syndrome.
    Amorim S, Heise CO, Santos S, Macedo-Souza LI, Zatz M, Kok F.
    Muscle Nerve; 2014 Jan; 49(1):131-3. PubMed ID: 24123118
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  • 18. Motor and sensory conduction velocity in patients with Charcot-Marie-Tooth disease exposed to carbon disulphide.
    Florescu A, Vasilescu C.
    Neurol Psychiatr (Bucur); 1976 Jan; 14(2):97-103. PubMed ID: 968423
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  • 19. [Subclinical lesions of peripheral nervous system in multiple sclerosis patients].
    Pogorzelski R, Baniukiewicz E, Drozdowski W.
    Neurol Neurochir Pol; 2004 Jan; 38(4):257-64. PubMed ID: 15383952
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  • 20. Cholinergic dysautonomia and Eaton-Lambert syndrome.
    Rubenstein AE, Horowitz SH, Bender AN.
    Neurology; 1979 May; 29(5):720-3. PubMed ID: 220562
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