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Journal Abstract Search

95 related items for PubMed ID: 5973942

  • 1. [Charcot-Marie-Tooth disease].
    Hausmanowa-Petrusewicz I, Jedrzejowska H, Dietrich-Rap Z.
    Rozpr Wydz Nauk Med; 1966; 11(2):81-106. PubMed ID: 5973942
    [No Abstract] [Full Text] [Related]

  • 2. [Familial neurogenic amyotrophy, similar to Charcot-Marie-Tooth disease. Clinical and ultrastructural study].
    Vital C, Julien J, Vallat JM, Le Blanc M.
    Rev Neurol (Paris); 1970 Jan; 122(1):15-28. PubMed ID: 5433253
    [No Abstract] [Full Text] [Related]

  • 3. Variability in nerve biopsy findings in a kinship with dominantly inherited Charcot-Marie-Tooth disease.
    Van Weerden TW, Houthoff HJ, Sie O, Minderhoud JM.
    Muscle Nerve; 1982 Mar; 5(3):185-96. PubMed ID: 7088015
    [No Abstract] [Full Text] [Related]

  • 4. [Early diagnosis and differentiation of Charcot-Marie neural atrophy].
    Lobzin VS, Saĭkova LA, Poliakova LA, Kosachev VD.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1984 Mar; 84(11):1601-5. PubMed ID: 6524176
    [Abstract] [Full Text] [Related]

  • 5. [Myopathis muscle tissue changes in cases of Charcot-Marie-Tooth progressive neuritic muscular atrophy].
    Cazzato G, Testa G.
    Acta Neurol (Napoli); 1969 Mar; 24(2):171-99. PubMed ID: 5386340
    [No Abstract] [Full Text] [Related]

  • 6. [Relationships between genotype and phenotype in Charcot-Marie-Tooth disease].
    Câmpeanu E, Morariu M.
    Rev Roum Neurol; 1970 Mar; 7(1):47-56. PubMed ID: 5527990
    [No Abstract] [Full Text] [Related]

  • 7. [Hypothyroid myopathies: optic and electron microscopic study before and after treatment].
    Vital C, Bergouignan M, Bataille JM.
    Rev Neurol (Paris); 1966 Nov; 115(5):971-2. PubMed ID: 5972500
    [No Abstract] [Full Text] [Related]

  • 8. [Electromyography in Charcot-Marie disease].
    Zumstein V, Schneider C.
    Schweiz Arch Neurol Neurochir Psychiatr; 1982 Nov; 130(2):297-307. PubMed ID: 7134908
    [No Abstract] [Full Text] [Related]

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  • 13. [The importance of studying stimulation parameters in amyotrophic lateral sclerosis and Charcot-Marie-Tooth neural amyotrophy].
    Kyral V, Pára F.
    Sb Ved Pr Lek Fak Karlovy Univerzity Hradci Kralove Suppl; 1980 Nov; 23(4):415-22. PubMed ID: 6971479
    [No Abstract] [Full Text] [Related]

  • 14. [Clinico-genetic considerations on Charcot-Marie-Tooth disease].
    Câmpeanu E, Morariu M.
    Neurol Psihiatr Neurochir; 1969 Nov; 14(4):313-22. PubMed ID: 5356058
    [No Abstract] [Full Text] [Related]

  • 15. [Sporadic distal myopathy].
    Il'ina NA, Aver'ianov IuN, Nechkina NP, Potomskaia LZ, Sokolina NA.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1983 Nov; 83(11):1620-3. PubMed ID: 6675357
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  • 17. [Charcot-Marie-Tooth disease and its surgical treatment].
    Pelc S, Toussaint J, Henry J.
    Acta Neurol Psychiatr Belg; 1966 Jul; 66(7):561-74. PubMed ID: 4961197
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  • 19. 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 Jul; 6(3):267-74. PubMed ID: 6090332
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  • 20. An unusual case with myotonia.
    Da YW, Wang M, Li Y, Lu Y, Jia JP.
    Kaohsiung J Med Sci; 2013 Mar; 29(3):172-5. PubMed ID: 23465422
    [Abstract] [Full Text] [Related]

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