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Journal Abstract Search

89 related items for PubMed ID: 11686409

  • 1. Ultrastructural findings in the peripheral nerve in a family with the intermediate form of Charcot-Marie-Tooth disease.
    Malandrini A, Ceuterick C, Villanova M, Gambelli S, Berti G, Rossi A, Guazzi GC.
    J Submicrosc Cytol Pathol; 2001; 33(1-2):59-63. PubMed ID: 11686409
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  • 2. [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; 53(3-B):560-9. PubMed ID: 8585811
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  • 3. Hypertrophic motor and sensory neuropathy type I (Charcot-Marie-Tooth disease): ultrastructural study of sural nerve biopsy in members of a family.
    Calore EE, Alonso Neto JL, Cavaliere MJ, Perez NM, Russo DH, Wakamatsu A, Maeda MY, Kitamura C.
    Pathologica; 1994 Jun; 86(3):279-83. PubMed ID: 7808799
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  • 4. The importance of quantitative electron microscopy in studying hypertrophic neuropathies. A comparison between a case of Déjérine Sottas disease (HMSN III) and a case of the hypertrophic form of Charcot-Marie-Tooth disease (HMSN I).
    Tredici G, Petruccioli-Pizzini MG, Gergely A, Coletti A.
    Int J Tissue React; 1984 Jun; 6(3):267-74. PubMed ID: 6090332
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  • 5. Clinical, electrophysiological and morphological findings of Charcot-Marie-Tooth neuropathy with vocal cord palsy and mutations in the GDAP1 gene.
    Sevilla T, Cuesta A, Chumillas MJ, Mayordomo F, Pedrola L, Palau F, Vílchez JJ.
    Brain; 2003 Sep; 126(Pt 9):2023-33. PubMed ID: 12821518
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  • 6. Hypertrophic Charcot-Marie-Tooth disease. Light and electron microscope studies of the sural nerve.
    Low PA, McLeod JG, Prineas JW.
    J Neurol Sci; 1978 Jan; 35(1):93-115. PubMed ID: 624962
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  • 7. Mild phenotype of Charcot-Marie-Tooth disease type 4B1.
    Murakami T, Kutoku Y, Nishimura H, Hayashi M, Abe A, Hayasaka K, Sunada Y.
    J Neurol Sci; 2013 Nov 15; 334(1-2):176-9. PubMed ID: 23962696
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  • 9. Clinical and pathological phenotype of the original family with Charcot-Marie-Tooth type 1B: a 20-year study.
    Bird TD, Kraft GH, Lipe HP, Kenney KL, Sumi SM.
    Ann Neurol; 1997 Apr 15; 41(4):463-9. PubMed ID: 9124803
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  • 10. Coexistence of Charcot Marie Tooth disease type 1A and diabetes in Taiwan: A clinicopathological study.
    Chao HC, Chou CT, Lee YC, Lin KP.
    J Neurol Sci; 2015 Nov 15; 358(1-2):213-20. PubMed ID: 26349404
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  • 12. 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
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  • 13. [Pathology of Charcot-Marie-Tooth Disease].
    Oka N.
    Brain Nerve; 2016 Jan 15; 68(1):21-9. PubMed ID: 26764296
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  • 14. A novel mutation, Thr65Ala, in the MPZ gene in a patient with Charcot-Marie-Tooth type 1B disease with focally folded myelin.
    Kochanski A, Drac H, Kabzińska D, Hausmanowa-Petrusewicz I.
    Neuromuscul Disord; 2004 Mar 15; 14(3):229-32. PubMed ID: 15036333
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  • 20. Clinicopathologic analysis of 124 biopsy-proven peripheral nerve diseases.
    Hong SM, Ha H, Suh JH, Kim KK, Khang SK, Ro JY, Park SH.
    J Korean Med Sci; 2000 Apr 15; 15(2):211-6. PubMed ID: 10803700
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