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Journal Abstract Search

141 related items for PubMed ID: 7421358

  • 1. [Familial hypertrophic neuropathies. Conceptual and critical outline. Report of a family with Dyck and Lambert's type IV disease (author's transl)].
    Sadaba Garay F, Franco Vicario R, Miguel de la Villa F, Ibarmia Lahuerta J, Bustamante Murga V.
    Med Clin (Barc); 1980 Oct 10; 75(6):240-6. PubMed ID: 7421358
    [Abstract] [Full Text] [Related]

  • 2. 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 10; 86(3):279-83. PubMed ID: 7808799
    [Abstract] [Full Text] [Related]

  • 3. [Formation of "onion bulbs" in Charcot-Marie-Tooth and Dejerine-Sottas hypertrophic neuropathies].
    Jedrzejowska H, Drac H, Sawicka E.
    Neuropatol Pol; 1975 Jun 10; 13(1):93-106. PubMed ID: 1118064
    [No Abstract] [Full Text] [Related]

  • 4. A family with Charcot-Marie-Tooth disease and Leber's optic atrophy.
    McLeod JG, Low PA, Morgan JA.
    Proc Aust Assoc Neurol; 1975 Jun 10; 12():23-5. PubMed ID: 1215391
    [Abstract] [Full Text] [Related]

  • 5. [Three cases of Charcot-Marie-Tooth disease with neural deafness-the classification and sural nerve pathology (author's transl)].
    Kim I, Ohnishi A, Kuroiwa Y.
    Rinsho Shinkeigaku; 1980 Apr 10; 20(4):264-70. PubMed ID: 7408330
    [No Abstract] [Full Text] [Related]

  • 6. [Roussy-Levy hereditary areflexic dysstasia. Its historical relation to Friedreich's disease, Charcot-Marie-Tooth atrophy and Dejerine-Sottas hypertrophic neuritis; the present status of the original family; the nosologic role of this entity].
    Lapresle J.
    Rev Neurol (Paris); 1982 Apr 10; 138(12):967-78. PubMed ID: 6763298
    [Abstract] [Full Text] [Related]

  • 7. Charcot-Marie-Tooth's disease with severe trophic and sensory disorders. Study of a case following along a half a century with anatomical studies.
    Barraquer-Bordas L, Navarro C, Salisachs P.
    Acta Neurol Latinoam; 1981 Apr 10; 27(3-4):177-89. PubMed ID: 6965173
    [Abstract] [Full Text] [Related]

  • 8. 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 10; 5(3):185-96. PubMed ID: 7088015
    [No Abstract] [Full Text] [Related]

  • 9. [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 10; 53(12):725-8. PubMed ID: 7155235
    [No Abstract] [Full Text] [Related]

  • 10. [Hereditary hypertrophic neuropathies--clinico-histopathological study].
    Krstić S, Dozić S, Gospavić J, Vidaković Z, Filipović B.
    Srp Arh Celok Lek; 1976 Sep 10; 104(9):625-37. PubMed ID: 1027118
    [No Abstract] [Full Text] [Related]

  • 11. [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 Sep 10; 33(3):303-7. PubMed ID: 7330503
    [No Abstract] [Full Text] [Related]

  • 12. [A family with progressive neural muscular atrophy--with special reference to relation with allied diseases (author's transl)].
    Hayashi Y, Tomita M, Shimizu K, Takamiya M, Watanabe H.
    Rinsho Shinkeigaku; 1978 Oct 10; 18(10):593-600. PubMed ID: 709963
    [No Abstract] [Full Text] [Related]

  • 13. 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 10; 41(4):463-9. PubMed ID: 9124803
    [Abstract] [Full Text] [Related]

  • 14. [Clinical electrodiagnostic findings in peroneal muscular atrophy (author's transl)].
    Leven B.
    Fortschr Neurol Psychiatr Grenzgeb; 1976 Nov 10; 44(11):661-70. PubMed ID: 1049563
    [Abstract] [Full Text] [Related]

  • 15. [Primary hypertrophic neuropathy in children. Apropos of a familial case].
    Talon P, Mair W, Beyer P.
    Ann Pediatr (Paris); 1983 Jan 10; 30(1):45-50. PubMed ID: 6830105
    [No Abstract] [Full Text] [Related]

  • 16. Endoneurial space and its constituents in the sural nerve of patients with neuropathy.
    Behse F, Buchthal F, Carlsen F, Knappeis GG.
    Brain; 1974 Dec 10; 97(4):773-84. PubMed ID: 4373123
    [No Abstract] [Full Text] [Related]

  • 17. [Morphological studies of peripheral nerves for a better understanding of Charcot-Marie-Tooth atrophy and Roussy-Lévy hereditary areflexic dysstasia].
    Lapresle J.
    Ann Med Interne (Paris); 1980 Dec 10; 131(7):397-400. PubMed ID: 7224445
    [Abstract] [Full Text] [Related]

  • 18. [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 Dec 10; 47(2):182-7. PubMed ID: 15776672
    [Abstract] [Full Text] [Related]

  • 19. [Usefulness Of electromyographic examination of families of patients affected with hypertrophic sensory-motor neuropathy (Charcot-Marie-Tooth disease). Preliminary results].
    Fardin P, Micaglio GF, Angelini C, Negrin P, Siciliano G.
    Riv Neurobiol; 1984 Dec 10; 30(2-3):222-8. PubMed ID: 6544478
    [No Abstract] [Full Text] [Related]

  • 20. [Hereditary motor and sensory neuropathy associated with retinitis pigmentosa and neural deafness].
    Murakami K, Sobue G, Takahashi A, Mitsuma T.
    Rinsho Shinkeigaku; 1986 Sep 10; 26(9):952-9. PubMed ID: 3791775
    [No Abstract] [Full Text] [Related]

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