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)

  • 21. 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; 12(1):59-68. PubMed ID: 9633821
    [TBL] [Abstract][Full Text] [Related]  

  • 22. De novo Ser72Leu mutation in the peripheral myelin protein 22 in two Polish patients with a severe form of Charcot-Marie-Tooth disease.
    Kochański A; Kabzińska D
    Acta Biochim Pol; 2004; 51(4):1047-50. PubMed ID: 15625576
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Schwann cells and the pathogenesis of inherited motor and sensory neuropathies (Charcot-Marie-Tooth disease).
    Berger P; Niemann A; Suter U
    Glia; 2006 Sep; 54(4):243-57. PubMed ID: 16856148
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Peripheral neuropathies caused by mutations in the myelin protein zero.
    Shy ME
    J Neurol Sci; 2006 Mar; 242(1-2):55-66. PubMed ID: 16414078
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Double trouble in hereditary neuropathy: concomitant mutations in the PMP-22 gene and another gene produce novel phenotypes.
    Hodapp JA; Carter GT; Lipe HP; Michelson SJ; Kraft GH; Bird TD
    Arch Neurol; 2006 Jan; 63(1):112-7. PubMed ID: 16401743
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Clinical features and molecular genetics of hereditary peripheral neuropathies.
    Kuhlenbäumer G; Young P; Hünermund G; Ringelstein B; Stögbauer F
    J Neurol; 2002 Dec; 249(12):1629-50. PubMed ID: 12529785
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Charcot-Marie-Tooth disease type I and related demyelinating neuropathies: Mutation analysis in a large cohort of Italian families.
    Mostacciuolo ML; Righetti E; Zortea M; Bosello V; Schiavon F; Vallo L; Merlini L; Siciliano G; Fabrizi GM; Rizzuto N; Milani M; Baratta S; Taroni F
    Hum Mutat; 2001; 18(1):32-41. PubMed ID: 11438991
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Major myelin protein gene (P0) mutation causes a novel form of axonal degeneration.
    Li J; Bai Y; Ianakova E; Grandis M; Uchwat F; Trostinskaia A; Krajewski KM; Garbern J; Kupsky WJ; Shy ME
    J Comp Neurol; 2006 Sep; 498(2):252-65. PubMed ID: 16856127
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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; 1991-1992; 25-26():97-107. PubMed ID: 11980069
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Molecular genetics of peripheral neuropathies.
    Harding AE
    Baillieres Clin Neurol; 1995 Nov; 4(3):383-400. PubMed ID: 8599717
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Molecular mechanisms for Charcot-Marie-Tooth disease and related demyelinating peripheral neuropathies.
    Warner LE; Reiter LT; Murakami T; Lupski JR
    Cold Spring Harb Symp Quant Biol; 1996; 61():659-71. PubMed ID: 9246492
    [No Abstract]   [Full Text] [Related]  

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

  • 33. Cochlear implantation in a patient with deafness induced by Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathies).
    Postelmans JT; Stokroos RJ
    J Laryngol Otol; 2006 Jun; 120(6):508-10. PubMed ID: 16772060
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A molecular genetic update of inherited distal motor neuropathies.
    Irobi-Devolder J
    Verh K Acad Geneeskd Belg; 2008; 70(1):25-46. PubMed ID: 18512357
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Evaluation of peripheral neuropathy. Part III: vasculitic, infectious, inherited, and idiopathic neuropathies.
    Kelly JJ
    Rev Neurol Dis; 2005; 2(2):70-9. PubMed ID: 19813300
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Molecular mechanisms of hereditary neuropathy: genotype-phenotype correlation].
    Nakagawa M; Takashima H
    Rinsho Byori; 2003 Jun; 51(6):536-43. PubMed ID: 12884740
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Common themes in peripheral neuropathy disease genes.
    Snipes GJ; Orfali W
    Cell Biol Int; 1998 Nov; 22(11-12):815-35. PubMed ID: 10873294
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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; 281(1-2):113-5. PubMed ID: 19344920
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Impaired intracellular trafficking is a common disease mechanism of PMP22 point mutations in peripheral neuropathies.
    Naef R; Suter U
    Neurobiol Dis; 1999 Feb; 6(1):1-14. PubMed ID: 10078969
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Skin biopsies in myelin-related neuropathies: bringing molecular pathology to the bedside.
    Li J; Bai Y; Ghandour K; Qin P; Grandis M; Trostinskaia A; Ianakova E; Wu X; Schenone A; Vallat JM; Kupsky WJ; Hatfield J; Shy ME
    Brain; 2005 May; 128(Pt 5):1168-77. PubMed ID: 15774502
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.