These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

189 related articles for article (PubMed ID: 8881422)

  • 1. Molecular pathogenesis of peripheral neuropathy.
    Trapp BD; Haney C; Yin X
    Rev Neurol (Paris); 1996 May; 152(5):314-9. PubMed ID: 8881422
    [TBL] [Abstract][Full Text] [Related]  

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

  • 3. Distinct disease mechanisms in peripheral neuropathies due to altered peripheral myelin protein 22 gene dosage or a Pmp22 point mutation.
    Giambonini-Brugnoli G; Buchstaller J; Sommer L; Suter U; Mantei N
    Neurobiol Dis; 2005 Apr; 18(3):656-68. PubMed ID: 15755691
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Evidence for macrophage-mediated myelin disruption in an animal model for Charcot-Marie-Tooth neuropathy type 1A.
    Kobsar I; Hasenpusch-Theil K; Wessig C; Müller HW; Martini R
    J Neurosci Res; 2005 Sep; 81(6):857-64. PubMed ID: 16041800
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular genetics of inherited peripheral neuropathies: who are the actors?
    Meuleman J; Timmerman V; Nelis E; De Jonghe P
    Acta Neurol Belg; 2000 Sep; 100(3):171-80. PubMed ID: 11098291
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular anatomy and genetics of myelin proteins in the peripheral nervous system.
    Snipes GJ; Suter U
    J Anat; 1995 Jun; 186 ( Pt 3)(Pt 3):483-94. PubMed ID: 7559122
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Hereditary neuropathies].
    Maisonobe T
    Rev Prat; 2000 Apr; 50(7):736-42. PubMed ID: 10853553
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Electrophysiologic features of inherited demyelinating neuropathies: a reappraisal.
    Lewis RA; Sumner AJ
    Ann N Y Acad Sci; 1999 Sep; 883():321-35. PubMed ID: 10586257
    [TBL] [Abstract][Full Text] [Related]  

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

  • 10. Balancing between adaptive and maladaptive cellular stress responses in peripheral neuropathy.
    Khajavi M; Lupski JR
    Neuron; 2008 Feb; 57(3):329-30. PubMed ID: 18255024
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [From gene to disease; Charcot-Marie-Tooth disease or the hereditary motor and sensory neuropathies].
    Verhamme C; Baas F
    Ned Tijdschr Geneeskd; 2005 Jul; 149(27):1505-9. PubMed ID: 16032995
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular alterations resulting from frameshift mutations in peripheral myelin protein 22: implications for neuropathy severity.
    Johnson JS; Roux KJ; Fletcher BS; Fortun J; Notterpek L
    J Neurosci Res; 2005 Dec; 82(6):743-52. PubMed ID: 16273544
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Novel mutations in the Charcot-Marie-Tooth disease genes PMP22, MPZ, and GJB1.
    Huehne K; Benes V; Thiel C; Kraus C; Kress W; Hoeltzenbein M; Ploner CJ; Kotzian J; Reis A; Rott HD; Rautenstrauss BW
    Hum Mutat; 2003 Jan; 21(1):100. PubMed ID: 12497641
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Charcot-Marie-Tooth disease and related peripheral neuropathies.
    De Jonghe P; Timmerman V; Nelis E; Martin JJ; Van Broeckhoven C
    J Peripher Nerv Syst; 1997; 2(4):370-87. PubMed ID: 10975746
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Role of immune cells in animal models for inherited peripheral neuropathies.
    Wang Ip C; Kroner A; Fischer S; Berghoff M; Kobsar I; Mäurer M; Martini R
    Neuromolecular Med; 2006; 8(1-2):175-90. PubMed ID: 16775375
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Normal expression of myelin protein zero with frame-shift mutation correlates with mild phenotype.
    Steck AJ; Erne B; Pareyson D; Sghirlanzoni A; Taroni F; Schaeren-Wiemers N
    J Peripher Nerv Syst; 2006 Mar; 11(1):61-6. PubMed ID: 16519783
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Regulation of myelin-specific gene expression. Relevance to CMT1.
    Kamholz J; Awatramani R; Menichella D; Jiang H; Xu W; Shy M
    Ann N Y Acad Sci; 1999 Sep; 883():91-108. PubMed ID: 10586235
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Phenotypic clustering in MPZ mutations.
    Shy ME; Jáni A; Krajewski K; Grandis M; Lewis RA; Li J; Shy RR; Balsamo J; Lilien J; Garbern JY; Kamholz J
    Brain; 2004 Feb; 127(Pt 2):371-84. PubMed ID: 14711881
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Many facets of the peripheral myelin protein PMP22 in myelination and disease.
    Naef R; Suter U
    Microsc Res Tech; 1998 Jun; 41(5):359-71. PubMed ID: 9672419
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.