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110 related items for PubMed ID: 9686263

  • 1. [Charcot-Marie-Tooth disease: electromyography is still useful in diagnosis and classification].
    Birouk N, Maisonobe T, Le Forestier N, Gouider R, Léger JM, Bouche P.
    Rev Neurol (Paris); 1997 Dec; 153(12):727-36. PubMed ID: 9686263
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  • 2. Molecular basis of hereditary neuropathies.
    Chance PF.
    Phys Med Rehabil Clin N Am; 2001 May; 12(2):277-91. PubMed ID: 11345007
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  • 3. [Molecular genetics of inherited neuropathies].
    Takashima H.
    Rinsho Shinkeigaku; 2006 Jan; 46(1):1-18. PubMed ID: 16541790
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  • 4. [Autosomal recessive forms of Charcot-Marie-Tooth disease].
    Vallat JM, Grid D, Magdelaine C, Sturtz F, Levy N, Tazir M.
    Bull Acad Natl Med; 2005 Jan; 189(1):55-68; discussion 68-9. PubMed ID: 16119880
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  • 5. [Different phenotypes of Charcot-Marie-Tooth disease caused by mutations in the same gene. Are classical criteria for classification still valid?].
    Sevilla T, Vílchez JJ.
    Neurologia; 2004 Jun; 19(5):264-71. PubMed ID: 15150710
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  • 9. Clinical, electrophysiological and molecular genetic studies in a family with X-linked dominant Charcot-Marie-Tooth neuropathy presenting a novel mutation in GJB1 Promoter and a rare polymorphism in LITAF/SIMPLE.
    Beauvais K, Furby A, Latour P.
    Neuromuscul Disord; 2006 Jan; 16(1):14-8. PubMed ID: 16373087
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  • 10. Assessment of axonal loss in Charcot-Marie-Tooth neuropathies.
    Lawson VH, Gordon Smith A, Bromberg MB.
    Exp Neurol; 2003 Dec; 184(2):753-7. PubMed ID: 14769367
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  • 13. Screening for mutations in the peripheral myelin genes PMP22, MPZ and Cx32 (GJB1) in Russian Charcot-Marie-Tooth neuropathy patients.
    Mersiyanova IV, Ismailov SM, Polyakov AV, Dadali EL, Fedotov VP, Nelis E, Löfgren A, Timmerman V, van Broeckhoven C, Evgrafov OV.
    Hum Mutat; 2000 Dec; 15(4):340-7. PubMed ID: 10737979
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  • 15. [Charcot-Marie-Tooth disease].
    Lee YC, Chang MH, Lin KP.
    Acta Neurol Taiwan; 2008 Sep; 17(3):203-13. PubMed ID: 18975529
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  • 17. [Charcot-Marie-Tooth disease associated with a pyramidal syndrome: clinical, electrophysiological, and neuropathological study of neuro-muscular biopsies in 14 cases].
    Thiam A, Sene FD, Ndao AK, Ndiaye M, Ndiaye IP.
    Dakar Med; 2002 Sep; 47(2):182-7. PubMed ID: 15776672
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  • 19. Neurophysiology and molecular genetics of Charcot-Marie-Tooth type 1 neuropathy in Croatian children: follow-up study.
    Barisić N, Mihatov I.
    Croat Med J; 2000 Sep; 41(3):306-13. PubMed ID: 10962051
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  • 20. Mild early onset axonal Charcot-Marie-Tooth disease not linked to other axonal Charcot-Marie-Tooth loci.
    Kochanski A, Kennerson M, Kawulak M, Ryniewicz B, Rowinska-Marcinska K, Walizada G, Nowakowski A, Hausmanowa-Petrusewicz I, Nicholson GA.
    Neurology; 2005 Feb 08; 64(3):533-5. PubMed ID: 15699389
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