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PUBMED FOR HANDHELDS

Journal Abstract Search


170 related items for PubMed ID: 22987707

  • 1. Spinal Charcot-Marie-Tooth disease: a reappraisal.
    Devic P, Petiot P, Mauguière F.
    Muscle Nerve; 2012 Oct; 46(4):604-9. PubMed ID: 22987707
    [Abstract] [Full Text] [Related]

  • 2. Charcot-Marie-Tooth disease.
    Martel J, Mierau D, Donat J.
    J Manipulative Physiol Ther; 1995 Oct; 18(3):168-71. PubMed ID: 7790797
    [Abstract] [Full Text] [Related]

  • 3. Charcot-Marie-Tooth type 2 and distal hereditary motor neuropathy: Clinical, neurophysiological and genetic findings from a single-centre experience.
    Luigetti M, Fabrizi GM, Bisogni G, Romano A, Taioli F, Ferrarini M, Bernardo D, Rossini PM, Sabatelli M.
    Clin Neurol Neurosurg; 2016 May; 144():67-71. PubMed ID: 26989944
    [Abstract] [Full Text] [Related]

  • 4. 2nd Workshop of the European CMT Consortium: 53rd ENMC International Workshop on Classification and Diagnostic Guidelines for Charcot-Marie-Tooth Type 2 (CMT2-HMSN II) and Distal Hereditary Motor Neuropathy (distal HMN-Spinal CMT) 26-28 September 1997, Naarden, The Netherlands.
    Neuromuscul Disord; 1998 Aug; 8(6):426-31. PubMed ID: 9713862
    [No Abstract] [Full Text] [Related]

  • 5. Clinical, electrophysiological and morphological findings of Charcot-Marie-Tooth neuropathy with vocal cord palsy and mutations in the GDAP1 gene.
    Sevilla T, Cuesta A, Chumillas MJ, Mayordomo F, Pedrola L, Palau F, Vílchez JJ.
    Brain; 2003 Sep; 126(Pt 9):2023-33. PubMed ID: 12821518
    [Abstract] [Full Text] [Related]

  • 6. Clinical and pathological phenotype of the original family with Charcot-Marie-Tooth type 1B: a 20-year study.
    Bird TD, Kraft GH, Lipe HP, Kenney KL, Sumi SM.
    Ann Neurol; 1997 Apr; 41(4):463-9. PubMed ID: 9124803
    [Abstract] [Full Text] [Related]

  • 7. Neurofibromatosis, Charcot-Marie-Tooth disease, or both?
    Roos KL, Pascuzzi RM, Dunn DW.
    Neurofibromatosis; 1989 Apr; 2(4):238-43. PubMed ID: 2517818
    [Abstract] [Full Text] [Related]

  • 8. Heat shock protein 27 R127W mutation: evidence of a continuum between axonal Charcot-Marie-Tooth and distal hereditary motor neuropathy.
    Solla P, Vannelli A, Bolino A, Marrosu G, Coviello S, Murru MR, Tranquilli S, Corongiu D, Benedetti S, Marrosu MG.
    J Neurol Neurosurg Psychiatry; 2010 Sep; 81(9):958-62. PubMed ID: 20660910
    [Abstract] [Full Text] [Related]

  • 9. 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
    [Abstract] [Full Text] [Related]

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  • 11. [Hereditary motor and sensory neuropathy (Charcot-Marie-Tooth disease). Molecular-genetic aspects].
    Hertz MJ, Jensen AD, Brandt CA, Bisgård C.
    Ugeskr Laeger; 1995 Jun 19; 157(25):3613-8. PubMed ID: 7652980
    [Abstract] [Full Text] [Related]

  • 12. [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 Jun 19; 47(2):182-7. PubMed ID: 15776672
    [Abstract] [Full Text] [Related]

  • 13. AAEE case report #20: hereditary motor and sensory neuropathy, type I.
    Chad DA.
    Muscle Nerve; 1989 Nov 19; 12(11):875-82. PubMed ID: 2608082
    [Abstract] [Full Text] [Related]

  • 14. [Molecular genetics of inherited neuropathies].
    Takashima H.
    Rinsho Shinkeigaku; 2006 Jan 19; 46(1):1-18. PubMed ID: 16541790
    [Abstract] [Full Text] [Related]

  • 15. Charcot-Marie-Tooth disease in northern Finland.
    Rantala H, Tolonen U, Myllylä V.
    Ann Clin Res; 1986 Jan 19; 18(3):154-9. PubMed ID: 3740791
    [Abstract] [Full Text] [Related]

  • 16. [Classification and molecular diagnostic procedure for Chacort-Marie-Tooth disease].
    Zhang RX, Tang BS.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Oct 19; 29(5):553-7. PubMed ID: 23042392
    [Abstract] [Full Text] [Related]

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  • 18. Clinical and electrophysiological aspects of Charcot-Marie-Tooth disease.
    Pareyson D, Scaioli V, Laurà M.
    Neuromolecular Med; 2006 Oct 19; 8(1-2):3-22. PubMed ID: 16775364
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  • 20. 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 19; 62(8):1201-7. PubMed ID: 16087758
    [Abstract] [Full Text] [Related]


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