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Journal Abstract Search


215 related items for PubMed ID: 624962

  • 21. Shortened internodal length of dermal myelinated nerve fibres in Charcot-Marie-Tooth disease type 1A.
    Saporta MA, Katona I, Lewis RA, Masse S, Shy ME, Li J.
    Brain; 2009 Dec; 132(Pt 12):3263-73. PubMed ID: 19923170
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  • 32. Endoneurial space and its constituents in the sural nerve of patients with neuropathy.
    Behse F, Buchthal F, Carlsen F, Knappeis GG.
    Brain; 1974 Dec; 97(4):773-84. PubMed ID: 4373123
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  • 35. Unmyelinated fibres and Schwann cells of sural nerve in neuropathy.
    Behse F, Buchthal F, Carlsen F, Knappeis GG.
    Brain; 1975 Sep; 98(3):493-510. PubMed ID: 171027
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  • 36. Effect of an R69C mutation in the myelin protein zero gene on myelination and ion channel subtypes.
    Bai Y, Ianokova E, Pu Q, Ghandour K, Levinson R, Martin JJ, Ceuterick-de Groote C, Mazanec R, Seeman P, Shy ME, Li J.
    Arch Neurol; 2006 Dec; 63(12):1787-94. PubMed ID: 17172621
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  • 37. Primary segmental demyelination in the sural nerve in Cockayne's syndrome.
    Ohnishi A, Mitsudome A, Murai Y.
    Muscle Nerve; 1987 Feb; 10(2):163-7. PubMed ID: 3821788
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  • 39. Hereditary motor sensory neuropathy type I presenting as scapuloperoneal atrophy (Davidenkow syndrome) electrophysiological and pathological studies.
    Ronen GM, Lowry N, Wedge JH, Sarnat HB, Hill A.
    Can J Neurol Sci; 1986 Aug; 13(3):264-6. PubMed ID: 3742344
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  • 40. Congenital hypomyelination polyneuropathy. Pathological findings compared with polyneuropathies starting later in life.
    Guzzetta F, Ferrière G, Lyon G.
    Brain; 1982 Jun; 105(Pt 2):395-416. PubMed ID: 7082995
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