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Journal Abstract Search

234 related items for PubMed ID: 10862406

  • 1. Small axons relative to number of myelin lamellae in Charcot-Marie-Tooth disease 1A with peripheral myelin protein 22 gene duplication.
    Ohnishi A, Yamamoto T, Ikeda M.
    J UOEH; 2000 Jun 01; 22(2):107-17. PubMed ID: 10862406
    [Abstract] [Full Text] [Related]

  • 2. Mutation-dependent alteration in cellular distribution of peripheral myelin protein 22 in nerve biopsies from Charcot-Marie-Tooth type 1A.
    Hanemann CO, D'Urso D, Gabreëls-Festen AA, Müller HW.
    Brain; 2000 May 01; 123 ( Pt 5)():1001-6. PubMed ID: 10775544
    [Abstract] [Full Text] [Related]

  • 3. Demyelinating and axonal features of Charcot-Marie-Tooth disease with mutations of myelin-related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patients.
    Hattori N, Yamamoto M, Yoshihara T, Koike H, Nakagawa M, Yoshikawa H, Ohnishi A, Hayasaka K, Onodera O, Baba M, Yasuda H, Saito T, Nakashima K, Kira J, Kaji R, Oka N, Sobue G, Study Group for Hereditary Neuropathy in Japan.
    Brain; 2003 Jan 01; 126(Pt 1):134-51. PubMed ID: 12477701
    [Abstract] [Full Text] [Related]

  • 4. [Charcot-Marie-Tooth disease. Study of sural nerve biopsy in 41 patients].
    Freitas MR, Nascimento OJ, Chimelli L, de Freitas GR.
    Arq Neuropsiquiatr; 1995 Sep 01; 53(3-B):560-9. PubMed ID: 8585811
    [Abstract] [Full Text] [Related]

  • 5. Abnormal Schwann cell-axon interactions in CMT neuropathies. The effects of mutant Schwann cells on the axonal cytoskeleton and regeneration-associated myelination.
    Sahenk Z.
    Ann N Y Acad Sci; 1999 Sep 14; 883():415-26. PubMed ID: 10586265
    [Abstract] [Full Text] [Related]

  • 6. Shortened internodal length of dermal myelinated nerve fibres in Charcot-Marie-Tooth disease type 1A.
    Saporta MA, Katona I, Lewis RA, Masse S, Shy ME, Li J.
    Brain; 2009 Dec 14; 132(Pt 12):3263-73. PubMed ID: 19923170
    [Abstract] [Full Text] [Related]

  • 7. A rat model of Charcot-Marie-Tooth disease 1A recapitulates disease variability and supplies biomarkers of axonal loss in patients.
    Fledrich R, Schlotter-Weigel B, Schnizer TJ, Wichert SP, Stassart RM, Meyer zu Hörste G, Klink A, Weiss BG, Haag U, Walter MC, Rautenstrauss B, Paulus W, Rossner MJ, Sereda MW.
    Brain; 2012 Jan 14; 135(Pt 1):72-87. PubMed ID: 22189569
    [Abstract] [Full Text] [Related]

  • 8. Effects of PMP22 duplication and deletions on the axonal cytoskeleton.
    Sahenk Z, Chen L, Mendell JR.
    Ann Neurol; 1999 Jan 14; 45(1):16-24. PubMed ID: 9894872
    [Abstract] [Full Text] [Related]

  • 9. Molecular and pathological studies in Charcot-Marie-Tooth disease 1A.
    Kosuka N, Tachi N, Ohya K, Chiba S.
    Brain Dev; 1997 Nov 14; 19(7):464-8. PubMed ID: 9408592
    [Abstract] [Full Text] [Related]

  • 10. Genetic epidemiology of Charcot-Marie-Tooth disease.
    Braathen GJ.
    Acta Neurol Scand Suppl; 2012 Nov 14; (193):iv-22. PubMed ID: 23106488
    [Abstract] [Full Text] [Related]

  • 11. Evidence for impaired axonal regeneration in PMP22 duplication: studies in nerve xenografts.
    Sahenk Z, Serrano-Munuera C, Chen L, Kakabadze I, Najagara HN.
    J Peripher Nerv Syst; 2003 Jun 14; 8(2):116-27. PubMed ID: 12795716
    [Abstract] [Full Text] [Related]

  • 12. Proliferation of Schwann cells and regulation of cyclin D1 expression in an animal model of Charcot-Marie-Tooth disease type 1A.
    Atanasoski S, Scherer SS, Nave KA, Suter U.
    J Neurosci Res; 2002 Feb 15; 67(4):443-9. PubMed ID: 11835311
    [Abstract] [Full Text] [Related]

  • 13. An essential role of MAG in mediating axon-myelin attachment in Charcot-Marie-Tooth 1A disease.
    Kinter J, Lazzati T, Schmid D, Zeis T, Erne B, Lützelschwab R, Steck AJ, Pareyson D, Peles E, Schaeren-Wiemers N.
    Neurobiol Dis; 2013 Jan 15; 49():221-31. PubMed ID: 22940629
    [Abstract] [Full Text] [Related]

  • 14. Charcot-Marie-Tooth disease and related peripheral neuropathies: novel mutations in the peripheral myelin genes connexin 32 (Cx32), peripheral myelin protein 22 (PMP22), and peripheral myelin protein zero (MPZ).
    Ekici AB, Schweitzer D, Park O, Lorek D, Rautenstrauss B, Krüger G, Friedl W, Uhlhaas S, Bathke K, Heuss D, Kayser C, Grehl H.
    Neurogenetics; 2000 Sep 15; 3(1):49-50. PubMed ID: 11085599
    [No Abstract] [Full Text] [Related]

  • 15. 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 15; 81(6):857-64. PubMed ID: 16041800
    [Abstract] [Full Text] [Related]

  • 16. Mutations in the MORC2 gene cause axonal Charcot-Marie-Tooth disease.
    Sevilla T, Lupo V, Martínez-Rubio D, Sancho P, Sivera R, Chumillas MJ, García-Romero M, Pascual-Pascual SI, Muelas N, Dopazo J, Vílchez JJ, Palau F, Espinós C.
    Brain; 2016 Jan 15; 139(Pt 1):62-72. PubMed ID: 26497905
    [Abstract] [Full Text] [Related]

  • 17. Charcot-Marie-Tooth disease type 1A: a clinical, electrophysiological, pathological, and genetic study.
    Hsieh SY, Kuo HC, Chu CC, Lin KP, Huang CC.
    Chang Gung Med J; 2004 Apr 15; 27(4):300-6. PubMed ID: 15239197
    [Abstract] [Full Text] [Related]

  • 18. Distal axonopathy in peripheral nerves of PMP22-mutant mice.
    Sancho S, Magyar JP, Aguzzi A, Suter1 U.
    Brain; 1999 Aug 15; 122 ( Pt 8)():1563-77. PubMed ID: 10430839
    [Abstract] [Full Text] [Related]

  • 19. Charcot-Marie-Tooth disease: histopathological features of the peripheral myelin protein (PMP22) duplication (CMT1A) and connexin32 mutations (CMTX1).
    Sander S, Nicholson GA, Ouvrier RA, McLeod JG, Pollard JD.
    Muscle Nerve; 1998 Feb 15; 21(2):217-25. PubMed ID: 9466597
    [Abstract] [Full Text] [Related]

  • 20. Accumulation of peripheral myelin protein 22 in onion bulbs and Schwann cells of biopsied nerves from patients with Charcot-Marie-Tooth disease type 1A.
    Nishimura T, Yoshikawa H, Fujimura H, Sakoda S, Yanagihara T.
    Acta Neuropathol; 1996 Nov 15; 92(5):454-60. PubMed ID: 8922056
    [Abstract] [Full Text] [Related]

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