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Journal Abstract Search

786 related items for PubMed ID: 18975529

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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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  • 9. [Study of the duplication of 17p11.2-12 chromosome region in the patients with hereditary motor and sensory neuropathy type 1A].
    Hryshchenko NV, Bychkova AM, Pichkur NA, Skyban HV, Dmytrenko VV, Livshyts' LA.
    Tsitol Genet; 2003 Jan; 37(6):55-9. PubMed ID: 15067947
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  • 10. Mechanisms of disease: inherited demyelinating neuropathies--from basic to clinical research.
    Nave KA, Sereda MW, Ehrenreich H.
    Nat Clin Pract Neurol; 2007 Aug; 3(8):453-64. PubMed ID: 17671523
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  • 11. [Advances in the molecular genetics of the hereditary neuropathies].
    Palau F, Cuesta A, Pedrola L.
    Rev Neurol; 2007 Aug; 35(3):246-53. PubMed ID: 12235587
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  • 12. Overview of hereditary neuropathy with liability to pressure palsies.
    Chance PF.
    Ann N Y Acad Sci; 1999 Sep 14; 883():14-21. PubMed ID: 10586225
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  • 16. Charcot-Marie-Tooth disease type 1A: molecular mechanisms of gene dosage and point mutation underlying a common inherited peripheral neuropathy.
    Roa BB, Garcia CA, Lupski JR.
    Int J Neurol; 1999 Sep 14; 25-26():97-107. PubMed ID: 11980069
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  • 17. Charcot-Marie-Tooth disease: a clinico-genetic confrontation.
    Barisic N, Claeys KG, Sirotković-Skerlev M, Löfgren A, Nelis E, De Jonghe P, Timmerman V.
    Ann Hum Genet; 2008 May 14; 72(Pt 3):416-41. PubMed ID: 18215208
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  • 19. [From gene to disease; Charcot-Marie-Tooth disease or the hereditary motor and sensory neuropathies].
    Verhamme C, Baas F.
    Ned Tijdschr Geneeskd; 2005 Jul 02; 149(27):1505-9. PubMed ID: 16032995
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  • 20. The various Charcot-Marie-Tooth diseases.
    Vallat JM, Mathis S, Funalot B.
    Curr Opin Neurol; 2013 Oct 02; 26(5):473-80. PubMed ID: 23945280
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