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Journal Abstract Search

441 related items for PubMed ID: 8585811

  • 1. [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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  • 2. 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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  • 4. 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; 41(4):463-9. PubMed ID: 9124803
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  • 7. [Charcot-Marie-Tooth neural muscular atrophy (HMSN type I) with isolated tumerous hypertrophy of the median nerve].
    Berger W, Goth D, Ketelsen U.
    Nervenarzt; 1982 Dec; 53(12):725-8. PubMed ID: 7155235
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  • 8. Nonmyelinating Schwann cell involvement with well-preserved unmyelinated axons in Charcot-Marie-Tooth disease type 1A.
    Koike H, Iijima M, Mori K, Yamamoto M, Hattori N, Katsuno M, Tanaka F, Watanabe H, Doyu M, Yoshikawa H, Sobue G.
    J Neuropathol Exp Neurol; 2007 Nov; 66(11):1027-36. PubMed ID: 17984684
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  • 9. [Charcot-Marie-Tooth disease associated with a pyramidal syndrome: clinical, electrophysiological, and neuropathological study of neuro-muscular biopsies in 14 cases].
    Thiam A, Sene FD, Ndao AK, Ndiaye M, Ndiaye IP.
    Dakar Med; 2002 Nov; 47(2):182-7. PubMed ID: 15776672
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  • 10. Primary segmental demyelination in the sural nerve in Cockayne's syndrome.
    Ohnishi A, Mitsudome A, Murai Y.
    Muscle Nerve; 1987 Feb; 10(2):163-7. PubMed ID: 3821788
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  • 12. 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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  • 13. 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 Jun 01; 33(1-2):59-63. PubMed ID: 11686409
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  • 14. Peroneal muscular atrophy (PMA) and related disorders. II. Histological findings in sural nerves.
    Behse F, Buchthal F.
    Brain; 1977 Mar 01; 100 Pt 1():67-85. PubMed ID: 861716
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  • 18. Similar clinical, pathological, and genetic features in Chinese patients with autosomal recessive and dominant Charcot-Marie-Tooth disease type 2K.
    Fu J, Dai S, Lu Y, Wu R, Wang Z, Yuan Y, Lv H.
    Neuromuscul Disord; 2017 Aug 01; 27(8):760-765. PubMed ID: 28495047
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  • 19. [Peripheral nerve abnormalities of mutant (PMA) mouse--myelinated fiber counts of sciatic, peroneal, sural and tibial nerves].
    Ohnishi A, Kuroiwa Y, Esaki K.
    No To Shinkei; 1986 Mar 01; 38(3):289-93. PubMed ID: 3707778
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