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Journal Abstract Search

235 related items for PubMed ID: 16458537

  • 21. Nerve conduction abnormalities and neuromyotonia in genetically engineered mouse models of human hereditary neuropathies.
    Zielasek J, Toyka KV.
    Ann N Y Acad Sci; 1999 Sep 14; 883():310-20. PubMed ID: 10586256
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  • 22. 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
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  • 25. 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
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  • 26. Preserved myelin integrity and reduced axonopathy in connexin32-deficient mice lacking the recombination activating gene-1.
    Kobsar I, Berghoff M, Samsam M, Wessig C, Mäurer M, Toyka KV, Martini R.
    Brain; 2003 Apr 01; 126(Pt 4):804-13. PubMed ID: 12615640
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  • 27. 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
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  • 30. 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 15; 11(3):281-6. PubMed ID: 7581451
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  • 32. Macrophage-related demyelination in peripheral nerves of mice deficient in the gap junction protein connexin 32.
    Kobsar I, Mäurer M, Ott T, Martini R.
    Neurosci Lett; 2002 Mar 01; 320(1-2):17-20. PubMed ID: 11849753
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  • 35. Electrophysiology of peripheral neuropathies--an overview.
    Gilliatt RW.
    Muscle Nerve; 1982 Mar 01; 5(9S):S108-16. PubMed ID: 6302486
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  • 38. Schwann cells and the pathogenesis of inherited motor and sensory neuropathies (Charcot-Marie-Tooth disease).
    Berger P, Niemann A, Suter U.
    Glia; 2006 Sep 01; 54(4):243-57. PubMed ID: 16856148
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  • 39. 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 01; 113(4):443-9. PubMed ID: 17294201
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  • 40. [Molecular genetics of inherited neuropathies].
    Takashima H.
    Rinsho Shinkeigaku; 2006 Jan 01; 46(1):1-18. PubMed ID: 16541790
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