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Journal Abstract Search

213 related items for PubMed ID: 19028581

  • 21. Demyelinating polyneuropathy with focally folded myelin sheaths in a family of Miniature Schnauzer dogs.
    Vanhaesebrouck AE, Couturier J, Cauzinille L, Mizisin AP, Shelton GD, Granger N.
    J Neurol Sci; 2008 Dec 15; 275(1-2):100-5. PubMed ID: 18809183
    [Abstract] [Full Text] [Related]

  • 22. Prolonged high frequency electrical stimulation is lethal to motor axons of mice heterozygously deficient for the myelin protein P₀ gene.
    Alvarez S, Moldovan M, Krarup C.
    Exp Neurol; 2013 Sep 15; 247():552-61. PubMed ID: 23439028
    [Abstract] [Full Text] [Related]

  • 23. Electrophysiology of peripheral neuropathies--an overview.
    Gilliatt RW.
    Muscle Nerve; 1982 Sep 15; 5(9S):S108-16. PubMed ID: 6302486
    [No Abstract] [Full Text] [Related]

  • 24. Strain-specific differences in the effects of cyclosporin A and FK506 on the survival and regeneration of axotomized retinal ganglion cells in adult rats.
    Cui Q, Hodgetts SI, Hu Y, Luo JM, Harvey AR.
    Neuroscience; 2007 May 25; 146(3):986-99. PubMed ID: 17408862
    [Abstract] [Full Text] [Related]

  • 25. An animal model for Charcot-Marie-Tooth disease type 4B1.
    Bonneick S, Boentert M, Berger P, Atanasoski S, Mantei N, Wessig C, Toyka KV, Young P, Suter U.
    Hum Mol Genet; 2005 Dec 01; 14(23):3685-95. PubMed ID: 16249189
    [Abstract] [Full Text] [Related]

  • 26. Localization and functional roles of PMP22 in peripheral nerves of P0-deficient mice.
    Carenini S, Neuberg D, Schachner M, Suter U, Martini R.
    Glia; 1999 Dec 01; 28(3):256-64. PubMed ID: 10559784
    [Abstract] [Full Text] [Related]

  • 27. Protein zero (P0)-deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathies.
    Martini R, Zielasek J, Toyka KV, Giese KP, Schachner M.
    Nat Genet; 1995 Nov 01; 11(3):281-6. PubMed ID: 7581451
    [Abstract] [Full Text] [Related]

  • 28. Visualization of degenerating axons in a dysmyelinating mouse mutant with axonal loss.
    Ey B, Kobsar I, Blazyca H, Kroner A, Martini R.
    Mol Cell Neurosci; 2007 May 01; 35(1):153-60. PubMed ID: 17383197
    [Abstract] [Full Text] [Related]

  • 29. Mtmr13/Sbf2-deficient mice: an animal model for CMT4B2.
    Tersar K, Boentert M, Berger P, Bonneick S, Wessig C, Toyka KV, Young P, Suter U.
    Hum Mol Genet; 2007 Dec 15; 16(24):2991-3001. PubMed ID: 17855448
    [Abstract] [Full Text] [Related]

  • 30. Heterozygous P0 deficiency protects mice from vincristine-induced polyneuropathy.
    Uçeyler N, Kobsar I, Biko L, Ulzheimer J, Levinson SR, Martini R, Sommer C.
    J Neurosci Res; 2006 Jul 15; 84(1):37-46. PubMed ID: 16676325
    [Abstract] [Full Text] [Related]

  • 31. Increase of MCP-1 (CCL2) in myelin mutant Schwann cells is mediated by MEK-ERK signaling pathway.
    Fischer S, Weishaupt A, Troppmair J, Martini R.
    Glia; 2008 Jun 15; 56(8):836-43. PubMed ID: 18383340
    [Abstract] [Full Text] [Related]

  • 32. [Charcot-Marie-Tooth disease].
    Okabe S, Gotoh J.
    Ryoikibetsu Shokogun Shirizu; 2000 Jun 15; (30 Pt 5):419-22. PubMed ID: 11057275
    [No Abstract] [Full Text] [Related]

  • 33. Accelerated demyelination of peripheral nerves in mice deficient in connexin 32 and protein zero.
    Neuberg DH, Carenini S, Schachner M, Martini R, Suter U.
    J Neurosci Res; 1998 Sep 01; 53(5):542-50. PubMed ID: 9726425
    [Abstract] [Full Text] [Related]

  • 34. Blocking mitochondrial calcium release in Schwann cells prevents demyelinating neuropathies.
    Gonzalez S, Berthelot J, Jiner J, Perrin-Tricaud C, Fernando R, Chrast R, Lenaers G, Tricaud N.
    J Clin Invest; 2016 Mar 01; 126(3):1023-38. PubMed ID: 26878172
    [Abstract] [Full Text] [Related]

  • 35. Immune deficiency in mouse models for inherited peripheral neuropathies leads to improved myelin maintenance.
    Schmid CD, Stienekemeier M, Oehen S, Bootz F, Zielasek J, Gold R, Toyka KV, Schachner M, Martini R.
    J Neurosci; 2000 Jan 15; 20(2):729-35. PubMed ID: 10632602
    [Abstract] [Full Text] [Related]

  • 36. Congenital hypomyelinating neuropathy, a long term follow-up study in an affected family.
    Smit LS, Roofthooft D, van Ruissen F, Baas F, van Doorn PA.
    Neuromuscul Disord; 2008 Jan 15; 18(1):59-62. PubMed ID: 17825553
    [Abstract] [Full Text] [Related]

  • 37. Diagnostic value of ultrastructural nerve examination in Charcot-Marie-Tooth disease: two CMT 1B cases with pseudo-recessive inheritance.
    Vallat JM, Magy L, Lagrange E, Sturtz F, Magdelaine C, Grid D, Tazir M.
    Acta Neuropathol; 2007 Apr 15; 113(4):443-9. PubMed ID: 17294201
    [Abstract] [Full Text] [Related]

  • 38. Differential changes in axonal conduction following CNS demyelination in two mouse models.
    Bando Y, Takakusaki K, Ito S, Terayama R, Kashiwayanagi M, Yoshida S.
    Eur J Neurosci; 2008 Nov 15; 28(9):1731-42. PubMed ID: 18973589
    [Abstract] [Full Text] [Related]

  • 39. 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]

  • 40. Efficient central nervous system remyelination requires T cells.
    Bieber AJ, Kerr S, Rodriguez M.
    Ann Neurol; 2003 May 15; 53(5):680-4. PubMed ID: 12731006
    [Abstract] [Full Text] [Related]

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