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Journal Abstract Search

924 related items for PubMed ID: 9124803

  • 21. 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; 62(8):1201-7. PubMed ID: 16087758
    [Abstract] [Full Text] [Related]

  • 22. [Molecular genetics of inherited neuropathies].
    Takashima H.
    Rinsho Shinkeigaku; 2006 Jan; 46(1):1-18. PubMed ID: 16541790
    [Abstract] [Full Text] [Related]

  • 23. [A gait disorder caused by hereditary motor-sensory neuropathy].
    Sauter R.
    Z Orthop Ihre Grenzgeb; 1990 Jan; 128(2):123-7. PubMed ID: 2140641
    [Abstract] [Full Text] [Related]

  • 24. [Hereditary neuropathy with liability to pressure palsies: study of six Spanish families].
    Pou Serradell A, Monells J, Téllez MJ, Fossas P, Löfgren A, Meuleman J, Timmerman V, De Jonghe P, Ceuterick C, Martin JJ.
    Rev Neurol (Paris); 2002 May; 158(5 Pt 1):579-88. PubMed ID: 12072826
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  • 25. [Charcot-Marie-Tooth disease. Study of sural nerve biopsy in 41 patients].
    Freitas MR, Nascimento OJ, Chimelli L, de Freitas GR.
    Arq Neuropsiquiatr; 1995 Sep; 53(3-B):560-9. PubMed ID: 8585811
    [Abstract] [Full Text] [Related]

  • 26. Overview of Charcot-Marie-Tooth disease type 1A.
    Thomas PK.
    Ann N Y Acad Sci; 1999 Sep 14; 883():1-5. PubMed ID: 10586223
    [Abstract] [Full Text] [Related]

  • 27. Inherited demyelinating neuropathies with micromutations of peripheral myelin protein 22 gene.
    Taioli F, Cabrini I, Cavallaro T, Acler M, Fabrizi GM.
    Brain; 2011 Feb 14; 134(Pt 2):608-17. PubMed ID: 21252112
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  • 32. Hemizygous mutation of the peripheral myelin protein 22 gene associated with Charcot-Marie-Tooth disease type 1.
    Numakura C, Lin C, Oka N, Akiguchi I, Hayasaka K.
    Ann Neurol; 2000 Jan 14; 47(1):101-3. PubMed ID: 10632107
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  • 34. Early onset neuropathy in a compound form of Charcot-Marie-Tooth disease.
    Meggouh F, de Visser M, Arts WF, De Coo RI, van Schaik IN, Baas F.
    Ann Neurol; 2005 Apr 14; 57(4):589-91. PubMed ID: 15786462
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  • 35. [Phenotypic heterogeneity in Japanese Charcot-Marie-Tooth disease type 1A patients with PMP-22 gene duplication].
    Yamamoto M, Sobue G, Yasuda T, Yamamoto K, Kumazawa K, Mitsuma T.
    Rinsho Shinkeigaku; 1995 Oct 14; 35(10):1085-91. PubMed ID: 8821490
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  • 37. A novel mutation, Thr65Ala, in the MPZ gene in a patient with Charcot-Marie-Tooth type 1B disease with focally folded myelin.
    Kochanski A, Drac H, Kabzińska D, Hausmanowa-Petrusewicz I.
    Neuromuscul Disord; 2004 Mar 14; 14(3):229-32. PubMed ID: 15036333
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  • 38. Gene dosage is a mechanism for Charcot-Marie-Tooth disease type 1A.
    Lupski JR, Wise CA, Kuwano A, Pentao L, Parke JT, Glaze DG, Ledbetter DH, Greenberg F, Patel PI.
    Nat Genet; 1992 Apr 14; 1(1):29-33. PubMed ID: 1301995
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