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Journal Abstract Search

404 related items for PubMed ID: 8752425

  • 1. [Mutation of the myelin Po gene in hereditary motor and sensory neuropathy].
    Hayasaka K.
    Rinsho Shinkeigaku; 1995 Dec; 35(12):1444-6. PubMed ID: 8752425
    [Abstract] [Full Text] [Related]

  • 2. Molecular basis of hereditary neuropathies.
    Chance PF.
    Phys Med Rehabil Clin N Am; 2001 May; 12(2):277-91. PubMed ID: 11345007
    [Abstract] [Full Text] [Related]

  • 3. Inherited peripheral neuropathy.
    Keller MP, Chance PF.
    Semin Neurol; 1999 May; 19(4):353-62. PubMed ID: 10716658
    [Abstract] [Full Text] [Related]

  • 4. [Genetics of peripheral neuropathies and hereditary ataxias].
    Palau F, Sevilla T.
    Neurologia; 1995 Dec; 10 Suppl 1():32-43. PubMed ID: 8838557
    [Abstract] [Full Text] [Related]

  • 5. Inherited neuropathies: Charcot-Marie-Tooth disease and related disorders.
    Chance PF, Lupski JR.
    Baillieres Clin Neurol; 1994 Aug; 3(2):373-85. PubMed ID: 7952853
    [Abstract] [Full Text] [Related]

  • 6. [Molecular basis of Charcot-Marie-Tooth neuropathy].
    Hayasaka K.
    Nihon Rinsho; 1996 Aug; 54(8):2243-51. PubMed ID: 8810804
    [Abstract] [Full Text] [Related]

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  • 8. Mutation testing in Charcot-Marie-Tooth neuropathy.
    Nicholson GA.
    Ann N Y Acad Sci; 1999 Sep 14; 883():383-8. PubMed ID: 10586262
    [Abstract] [Full Text] [Related]

  • 9. Mutations in the myelin protein zero gene associated with Charcot-Marie-Tooth disease type 1B.
    Latour P, Blanquet F, Nelis E, Bonnebouche C, Chapon F, Diraison P, Ollagnon E, Dautigny A, Pham-Dinh D, Chazot G.
    Hum Mutat; 1995 Sep 14; 6(1):50-4. PubMed ID: 7550231
    [Abstract] [Full Text] [Related]

  • 10. Genetic evaluation of inherited motor/sensory neuropathy.
    Chance PF.
    Suppl Clin Neurophysiol; 2004 Sep 14; 57():228-42. PubMed ID: 16106622
    [Abstract] [Full Text] [Related]

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  • 12. Mutations in the peripheral myelin genes and associated genes in inherited peripheral neuropathies.
    Nelis E, Haites N, Van Broeckhoven C.
    Hum Mutat; 1999 Sep 14; 13(1):11-28. PubMed ID: 9888385
    [Abstract] [Full Text] [Related]

  • 13. Genetic basis of inherited peripheral neuropathies.
    Suter U, Patel PI.
    Hum Mutat; 1994 Sep 14; 3(2):95-102. PubMed ID: 7515304
    [Abstract] [Full Text] [Related]

  • 14. Spectrum of mutations in Finnish patients with Charcot-Marie-Tooth disease and related neuropathies.
    Silander K, Meretoja P, Juvonen V, Ignatius J, Pihko H, Saarinen A, Wallden T, Herrgård E, Aula P, Savontaus ML.
    Hum Mutat; 1998 Sep 14; 12(1):59-68. PubMed ID: 9633821
    [Abstract] [Full Text] [Related]

  • 15. Dejerine-Sottas syndrome associated with point mutation in the peripheral myelin protein 22 (PMP22) gene.
    Roa BB, Dyck PJ, Marks HG, Chance PF, Lupski JR.
    Nat Genet; 1993 Nov 14; 5(3):269-73. PubMed ID: 8275092
    [Abstract] [Full Text] [Related]

  • 16. A novel homozygous mutation of the myelin Po gene producing Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III).
    Ikegami T, Nicholson G, Ikeda H, Ishida A, Johnston H, Wise G, Ouvrier R, Hayasaka K.
    Biochem Biophys Res Commun; 1996 May 06; 222(1):107-10. PubMed ID: 8630052
    [Abstract] [Full Text] [Related]

  • 17. Inherited neuropathies: from gene to disease.
    Keller MP, Chance PF.
    Brain Pathol; 1999 Apr 06; 9(2):327-41. PubMed ID: 10219749
    [Abstract] [Full Text] [Related]

  • 18. Severe demyelinating hypertrophic polyneuropathy caused by a de novo frameshift mutation within the intracellular domain of myelin protein zero (MPZ/P0).
    Zschüntzsch J, Dibaj P, Pilgram S, Kötting J, Gerding WM, Neusch C.
    J Neurol Sci; 2009 Jun 15; 281(1-2):113-5. PubMed ID: 19344920
    [Abstract] [Full Text] [Related]

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  • 20. 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 Jun 15; 15(4):340-7. PubMed ID: 10737979
    [Abstract] [Full Text] [Related]

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