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PUBMED FOR HANDHELDS

Journal Abstract Search

268 related items for PubMed ID: 829740

  • 1. Peroneal musclar atrophy (of Charcot-Marie-Tooth) in two African brothers.
    Billinghurst JR.
    Afr J Med Med Sci; 1976 Dec; 5(4):269-72. PubMed ID: 829740
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  • 3. Dominantly inherited peroneal muscular atrophy (hereditary motor and sensory neuropathy type I) in infancy and childhood.
    Vanasse M, Dubowitz V.
    Muscle Nerve; 1981 Dec; 4(1):26-30. PubMed ID: 7231442
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  • 5. [Charcot-Marie-Tooth disease. Report of a family (author's transl)].
    Alonso ME, Figueroa HH, Zermeño F, Escobar A, Flores T.
    Rev Invest Clin; 1981 Dec; 33(3):303-7. PubMed ID: 7330503
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  • 6. Neurophysiology and molecular genetics of Charcot-Marie-Tooth type 1 neuropathy in Croatian children: follow-up study.
    Barisić N, Mihatov I.
    Croat Med J; 2000 Sep; 41(3):306-13. PubMed ID: 10962051
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  • 7. A family with Charcot-Marie-Tooth disease and Leber's optic atrophy.
    McLeod JG, Low PA, Morgan JA.
    Proc Aust Assoc Neurol; 1975 Sep; 12():23-5. PubMed ID: 1215391
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  • 8. Genetic linkage evidence for heterogeneity in Charcot-Marie-Tooth neuropathy (HMSN type I).
    Bird TD, Ott J, Giblett ER, Chance PF, Sumi SM, Kraft GH.
    Ann Neurol; 1983 Dec; 14(6):679-84. PubMed ID: 6651251
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  • 12. Neuromyotonia in the spinal form of Charcot-Marie-Tooth disease.
    Lance JW, Durke D, Pollard J.
    Clin Exp Neurol; 1979 Dec; 16():49-56. PubMed ID: 550956
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  • 13. Clinical and electrophysiological characteristics of autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2B) that maps to chromosome 19q13.3.
    Berghoff C, Berghoff M, Leal A, Morera B, Barrantes R, Reis A, Neundörfer B, Rautenstrauss B, Del Valle G, Heuss D.
    Neuromuscul Disord; 2004 May; 14(5):301-6. PubMed ID: 15099588
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  • 14. Pathogenesis of Charcot-Marie-Tooth disease. Gait analysis and electrophysiologic, genetic, histopathologic, and enzyme studies in a kinship.
    Sabir M, Lyttle D.
    Clin Orthop Relat Res; 1984 Apr; (184):223-35. PubMed ID: 6705352
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