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Journal Abstract Search

162 related items for PubMed ID: 7964809

  • 21. Pattern of sensory conduction in Guillain-Barre Syndrome.
    Bansal R, Kalita J, Misra UK.
    Electromyogr Clin Neurophysiol; 2001; 41(7):433-7. PubMed ID: 11721299
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  • 22. Distal amyotrophy of predominantly the upper limbs with pyramidal features in a large kinship.
    van Gent EM, Hoogland RA, Jennekens FG.
    J Neurol Neurosurg Psychiatry; 1985 Mar; 48(3):266-9. PubMed ID: 3981197
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  • 25. Dominantly inherited hypertrophic neuropathy.
    Mongia SK, Ghanem Q, Preston D, Lewis AJ, Atack EA.
    Can J Neurol Sci; 1978 May; 5(2):239-46. PubMed ID: 667751
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  • 27. Wide spectrum of motor conduction velocity in Charcot-Marie-Tooth disease. An anatomico-physiological interpretation.
    Salisachs P.
    J Neurol Sci; 1974 Sep; 23(1):25-31. PubMed ID: 4855423
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  • 28. F-wave velocity in the central segment of the median and ulnar nerves. A study in normal subjects and in patients with Charcot-Marie-Tooth disease.
    Kimura J.
    Neurology; 1974 Jun; 24(6):539-46. PubMed ID: 4857549
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  • 35. The electrophysiological profile of hereditary motor and sensory neuropathy-Lom.
    Ishpekova BA, Christova LG, Alexandrov AS, Thomas PK.
    J Neurol Neurosurg Psychiatry; 2005 Jun; 76(6):875-8. PubMed ID: 15897517
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  • 36. The peroneal muscular atrophy syndrome: clinical, genetic, electrophysiological and nerve biopsy studies. I. Clinical, genetic and electrophysiological findings and classification.
    Davis CJ, Bradley WG, Madrid R.
    J Genet Hum; 1978 Dec; 26(4):311-49. PubMed ID: 752065
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  • 39. Hereditary motor sensory neuropathy type II with neurofilament accumulation: new finding or new disorder?
    Vogel P, Gabriel M, Goebel HH, Dyck PJ.
    Ann Neurol; 1985 May; 17(5):455-61. PubMed ID: 3859241
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  • 40. [Clinical electrophysiological studies of peroneal muscular atrophy--report of 32 cases].
    Cui LY.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1989 Jun; 11(3):175-9. PubMed ID: 2529984
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