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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

178 related items for PubMed ID: 7885014

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  • 26. Dejerine-Sottas disease and hereditary demyelinating polyneuropathy of infancy.
    Plante-Bordeneuve V, Said G.
    Muscle Nerve; 2002 Nov; 26(5):608-21. PubMed ID: 12402282
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  • 27. [A family of X-linked motor and sensory neuropathy with a new type of connexin32 mutation].
    Ohnishi A, Yoshimura T, Takazawa A, Hashimoto T, Yamamoto T, Fukushima Y.
    Rinsho Shinkeigaku; 1995 Aug; 35(8):843-9. PubMed ID: 8665724
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  • 29. A novel homozygous mutation of the myelin Po gene producing Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III).
    Ikegami T, Nicholson G, Ikeda H, Ishida A, Johnston H, Wise G, Ouvrier R, Hayasaka K.
    Biochem Biophys Res Commun; 1996 May 06; 222(1):107-10. PubMed ID: 8630052
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  • 33. A Japanese family with early-onset ataxia with motor and sensory neuropathy.
    Kobayashi S, Takuma H, Murayama S, Sakurai M, Kanazawa I.
    J Neurol Sci; 2007 Mar 15; 254(1-2):44-8. PubMed ID: 17258771
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  • 37. [Congenital hereditary motor and sensory neuropathy].
    Routon MC, Robain O, Mayer M, Jardin L, Ponsot G.
    Rev Neurol (Paris); 1991 Mar 15; 147(8-9):577-85. PubMed ID: 1962067
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  • 40. Severe infantile neuropathy with diaphragmatic weakness and its relationship to SMARD1.
    Pitt M, Houlden H, Jacobs J, Mok Q, Harding B, Reilly M, Surtees R.
    Brain; 2003 Dec 15; 126(Pt 12):2682-92. PubMed ID: 14506069
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