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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

142 related items for PubMed ID: 4467779

  • 21. Subacute-chronic polyneuritis.
    Poewe W, Sluga E, Aichner F.
    Acta Neuropathol Suppl; 1981; 7():262-7. PubMed ID: 6939249
    [No Abstract] [Full Text] [Related]

  • 22.
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  • 24. [Charcot-Marie-Tooth disease in a Belgian family. Relative frequency of pes cavus and of abnormalities of nerve conduction. Preliminary note].
    Burguet W, Hennen G, Chantraine A, Dodinval P.
    J Neurol Sci; 1967; 4(3):559-70. PubMed ID: 6051757
    [No Abstract] [Full Text] [Related]

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  • 26. Conjugal motor neuron disease.
    Chad D, Mitsumoto H, Adelman LS, Bradley WG, Munsat TL, Zieper I.
    Neurology; 1982 Mar; 32(3):306-7. PubMed ID: 7199646
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  • 28. 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
    [Abstract] [Full Text] [Related]

  • 29. Peroneal muscular atrophy (PMA) and related disorders. I. Clinical manifestations as related to biopsy findings, nerve conduction and electromyography.
    Buchthal F, Behse F.
    Brain; 1977 Mar; 100 Pt 1():41-66. PubMed ID: 861715
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  • 31. Motor nerve conduction velocity in anterior horn lesions.
    Hausmanowa-Petrusewicz I, Kopeć J.
    Electromyography; 1970 Mar; 10(3):227-37. PubMed ID: 5509969
    [No Abstract] [Full Text] [Related]

  • 32. [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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  • 33. [Congenital centronuclear myopathy. Two morphological variants in one family (author's transl)].
    Pongratz D, Weindl A, Reichl W, Koppenwallner C, Heuser M, Hübner G.
    Klin Wochenschr; 1976 May 01; 54(9):423-30. PubMed ID: 131874
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  • 34. [Four cases of hereditary motor and sensory neuropathy in childhood--light and electron microscopic studies of sural nerve biopsies].
    Sugie Y, Sugama M, Sugama S, Kosaka S, Shibuya T, Sugie H, Fukuyama Y.
    No To Hattatsu; 1985 Nov 01; 17(6):500-6. PubMed ID: 4084416
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  • 36. Spinal muscular atrophy: foetal-like histopathological pattern in Werdnig-Hoffmann disease.
    Hausmanowa-Petrusewicz I, Fidzianska A.
    Bull N Y Acad Med; 1974 Dec 01; 50(11):1157-72. PubMed ID: 4529631
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  • 38. Hereditary canine spinal muscular atrophy.
    Cork LC, Griffin JW, Munnell JF, Lorenz MD, Adams RJ.
    J Neuropathol Exp Neurol; 1979 May 01; 38(3):209-21. PubMed ID: 438862
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  • 39. Peripheral motor neuropathy associated with autonomic dysfunction in two sisters: new hereditary syndrome?
    Lisker R, García-Ramos G, de la Rosa-Laris C, Díaz-Mitoma F.
    Am J Med Genet; 1981 May 01; 9(3):255-9. PubMed ID: 7282784
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  • 40. 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 01; 17(5):455-61. PubMed ID: 3859241
    [Abstract] [Full Text] [Related]

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