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Journal Abstract Search

335 related items for PubMed ID: 7397478

  • 1. 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. 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
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  • 9. [Hereditary motor and sensory neuropathy. I. Principles of classification and clinical picture].
    Badurska B, Jedrzejowska H, Ryniewicz B, Drac H.
    Neurol Neurochir Pol; 1986 Nov; 20(1):24-8. PubMed ID: 3012388
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  • 12. Hereditary motor and sensory neuropathy. Clinical, genetic and electrodiagnostic studies.
    Vasilescu C.
    Rom J Neurol Psychiatry; 1993 Nov; 31(3-4):207-19. PubMed ID: 8011484
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  • 14. Dominantly inherited peroneal muscular atrophy (hereditary motor and sensory neuropathy type I) in infancy and childhood.
    Vanasse M, Dubowitz V.
    Muscle Nerve; 1981 Nov; 4(1):26-30. PubMed ID: 7231442
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  • 15. [Subclinical lesions of peripheral nervous system in multiple sclerosis patients].
    Pogorzelski R, Baniukiewicz E, Drozdowski W.
    Neurol Neurochir Pol; 2004 Nov; 38(4):257-64. PubMed ID: 15383952
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  • 16. Nerve conduction impairment in patients with respiratory insufficiency and severe chronic hypoxemia.
    Narayan M, Ferranti R.
    Arch Phys Med Rehabil; 1978 Apr; 59(4):188-92. PubMed ID: 646609
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  • 19. [Evaluation of polyneuropathy severity in chronic renal failure patients on continuous ambulatory peritoneal dialysis or on maintenance hemodialysis].
    Janda K, Stompór T, Gryz E, Szczudlik A, Drozdz M, Kraśniak A, Sułowicz W.
    Przegl Lek; 2007 Apr; 64(6):423-30. PubMed ID: 18159852
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  • 20. Hereditary motor and sensory neuropathy: HMSN type II (neuronal type) and X-linked HMSN.
    Hahn AF.
    Brain Pathol; 1993 Apr; 3(2):147-55. PubMed ID: 8293176
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