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Journal Abstract Search

190 related items for PubMed ID: 22271166

  • 1. Vincristine exacerbates asymptomatic Charcot-Marie-tooth disease with a novel EGR2 mutation.
    Nakamura T, Hashiguchi A, Suzuki S, Uozumi K, Tokunaga S, Takashima H.
    Neurogenetics; 2012 Feb; 13(1):77-82. PubMed ID: 22271166
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  • 2. Genetic epidemiology of Charcot-Marie-Tooth disease.
    Braathen GJ.
    Acta Neurol Scand Suppl; 2012 Feb; (193):iv-22. PubMed ID: 23106488
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  • 3. 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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  • 4. Charcot-Marie-Tooth disease and related inherited neuropathies.
    Murakami T, Garcia CA, Reiter LT, Lupski JR.
    Medicine (Baltimore); 1996 Sep 30; 75(5):233-50. PubMed ID: 8862346
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  • 5. A novel EGR2 mutation within a family with a mild demyelinating form of Charcot-Marie-Tooth disease.
    Shiga K, Noto Y, Mizuta I, Hashiguchi A, Takashima H, Nakagawa M.
    J Peripher Nerv Syst; 2012 Jun 30; 17(2):206-9. PubMed ID: 22734907
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  • 6. The EGR2 gene is involved in axonal Charcot-Marie-Tooth disease.
    Sevilla T, Sivera R, Martínez-Rubio D, Lupo V, Chumillas MJ, Calpena E, Dopazo J, Vílchez JJ, Palau F, Espinós C.
    Eur J Neurol; 2015 Dec 30; 22(12):1548-55. PubMed ID: 26204789
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  • 12. Mutation analysis of PMP22 in Slovak patients with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies.
    Resko P, Radvansky J, Odnogova Z, Baldovic M, Minarik G, Polakova H, Palffy R, Kadasi L.
    Gen Physiol Biophys; 2011 Dec 30; 30(4):379-88. PubMed ID: 22131320
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  • 14. Successful alternative treatment containing vindesine for acute lymphoblastic leukemia with Charcot-Marie-Tooth disease.
    Ichikawa M, Suzuki D, Inamoto J, Ohshima J, Cho Y, Saitoh S, Kaneda M, Iguchi A, Ariga T.
    J Pediatr Hematol Oncol; 2012 Apr 30; 34(3):239-41. PubMed ID: 22246157
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  • 15. Two missense mutations of EGR2 R359W and GJB1 V136A in a Charcot-Marie-Tooth disease family.
    Chung KW, Sunwoo IN, Kim SM, Park KD, Kim WK, Kim TS, Koo H, Cho M, Lee J, Choi BO.
    Neurogenetics; 2005 Sep 30; 6(3):159-63. PubMed ID: 15947997
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  • 16. A de novo EGR2 variant, c.1232A > G p.Asp411Gly, causes severe early-onset Charcot-Marie-Tooth Neuropathy Type 3 (Dejerine-Sottas Neuropathy).
    Grosz BR, Golovchenko NB, Ellis M, Kumar K, Nicholson GA, Antonellis A, Kennerson ML.
    Sci Rep; 2019 Dec 18; 9(1):19336. PubMed ID: 31852952
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  • 20. Charcot-Marie-Tooth disease type 1A: a clinical, electrophysiological, pathological, and genetic study.
    Hsieh SY, Kuo HC, Chu CC, Lin KP, Huang CC.
    Chang Gung Med J; 2004 Apr 18; 27(4):300-6. PubMed ID: 15239197
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