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Journal Abstract Search

309 related items for PubMed ID: 12661049

  • 1. Inherited polyneuropathy in Leonberger dogs: a mixed or intermediate form of Charcot-Marie-Tooth disease?
    Shelton GD, Podell M, Poncelet L, Schatzberg S, Patterson E, Powell HC, Mizisin AP.
    Muscle Nerve; 2003 Apr; 27(4):471-7. PubMed ID: 12661049
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  • 2. [Molecular genetics of inherited neuropathies].
    Takashima H.
    Rinsho Shinkeigaku; 2006 Jan; 46(1):1-18. PubMed ID: 16541790
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  • 3. [An unusual case of peroneal muscular atrophy with rigidity, polyneuropathy, mental retardation, and diabetes mellitus developed in familial Parkinson's disease].
    Saito T, Hosoda M, Aoto K, Hasegawa H, Kowa H.
    Rinsho Shinkeigaku; 1995 Aug; 35(8):878-83. PubMed ID: 8665730
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  • 4. Motor axonal sprouting and neuromuscular junction loss in an animal model of Charcot-Marie-Tooth disease.
    Ang ET, Schäfer R, Baltensperger R, Wernig A, Celio M, Oliver SS.
    J Neuropathol Exp Neurol; 2010 Mar; 69(3):281-93. PubMed ID: 20142762
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  • 5. Clinical and electrophysiological characteristics of autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2B) that maps to chromosome 19q13.3.
    Berghoff C, Berghoff M, Leal A, Morera B, Barrantes R, Reis A, Neundörfer B, Rautenstrauss B, Del Valle G, Heuss D.
    Neuromuscul Disord; 2004 May; 14(5):301-6. PubMed ID: 15099588
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  • 6. Phenotypic spectrum of disorders associated with glycyl-tRNA synthetase mutations.
    Sivakumar K, Kyriakides T, Puls I, Nicholson GA, Funalot B, Antonellis A, Sambuughin N, Christodoulou K, Beggs JL, Zamba-Papanicolaou E, Ionasescu V, Dalakas MC, Green ED, Fischbeck KH, Goldfarb LG.
    Brain; 2005 Oct; 128(Pt 10):2304-14. PubMed ID: 16014653
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  • 13. Demyelinating polyneuropathy with focally folded myelin sheaths in a family of Miniature Schnauzer dogs.
    Vanhaesebrouck AE, Couturier J, Cauzinille L, Mizisin AP, Shelton GD, Granger N.
    J Neurol Sci; 2008 Dec 15; 275(1-2):100-5. PubMed ID: 18809183
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  • 17. [A family of early childhood-onset Charcot-Marie-Tooth disease type 2].
    Hinuma Y, Aoki M, Takahashi T, Tateyama M, Nagai M, Yoshioka M, Itoyama Y.
    Rinsho Shinkeigaku; 2001 Jan 15; 41(1):64-7. PubMed ID: 11433771
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  • 18. Mutation analysis of the small heat shock protein 27 gene in chinese patients with Charcot-Marie-Tooth disease.
    Tang B, Liu X, Zhao G, Luo W, Xia K, Pan Q, Cai F, Hu Z, Zhang C, Chen B, Zhang F, Shen L, Zhang R, Jiang H.
    Arch Neurol; 2005 Aug 15; 62(8):1201-7. PubMed ID: 16087758
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