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303 related items for PubMed ID: 10775544

  • 1. 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; 123 ( Pt 5)():1001-6. PubMed ID: 10775544
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  • 2. Inherited demyelinating neuropathies with micromutations of peripheral myelin protein 22 gene.
    Taioli F, Cabrini I, Cavallaro T, Acler M, Fabrizi GM.
    Brain; 2011 Feb; 134(Pt 2):608-17. PubMed ID: 21252112
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  • 3. 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
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  • 4. Peripheral myelin protein-22 expression in Charcot-Marie-Tooth disease type 1a sural nerve biopsies.
    Hanemann CO, Stoll G, D'Urso D, Fricke W, Martin JJ, Van Broeckhoven C, Mancardi GL, Bartke I, Müller HW.
    J Neurosci Res; 1994 Apr 01; 37(5):654-9. PubMed ID: 8028042
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  • 5. Tomaculous neuropathy in chromosome 1 Charcot-Marie-Tooth syndrome.
    Thomas FP, Lebo RV, Rosoklija G, Ding XS, Lovelace RE, Latov N, Hays AP.
    Acta Neuropathol; 1994 Apr 01; 87(1):91-7. PubMed ID: 7511317
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  • 6. Schwann cell differentiation in Charcot-Marie-Tooth disease type 1A (CMT1A): normal number of myelinating Schwann cells in young CMT1A patients and neural cell adhesion molecule expression in onion bulbs.
    Hanemann CO, Gabreëls-Festen AA, Stoll G, Müller HW.
    Acta Neuropathol; 1997 Oct 01; 94(4):310-5. PubMed ID: 9341930
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  • 7. 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
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  • 10. Screening for Charcot-Marie-Tooth type 1A and hereditary neuropathy with liability to pressure palsy in archival nerve biopsy samples by direct-double-differential PCR.
    Beckmann A, Schröder JM.
    Acta Neuropathol; 2000 Nov 01; 100(5):459-63. PubMed ID: 11045666
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  • 16. 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 01; 21(2):217-25. PubMed ID: 9466597
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  • 18. The modifying effect a PMP22 deletion in a family with Charcot-Marie-Tooth type 1 neuropathy due to an EGR2 mutation.
    Reményi V, Inczédy-Farkas G, Gál A, Bereznai B, Pál Z, Karcagi V, Mechler F, Molnár MJ.
    Ideggyogy Sz; 2014 Nov 30; 67(11-12):420-5. PubMed ID: 25720245
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