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468 related items for PubMed ID: 1215391

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

  • 2. Leber's optic neuropathy and Charcot-Marie-Tooth disease. Report of a case.
    McCluskey DJ, O'Connor PS, Sheehy JT.
    J Clin Neuroophthalmol; 1986 Jun; 6(2):76-81. PubMed ID: 2942573
    [Abstract] [Full Text] [Related]

  • 3. Charcot-Marie-Tooth disease with Leber optic atrophy.
    McLeod JG, Low PA, Morgan JA.
    Neurology; 1978 Feb; 28(2):179-84. PubMed ID: 563998
    [Abstract] [Full Text] [Related]

  • 4. [Leber's optic atrophy - an interdisciplinary study (author's transl)].
    Müller-Jensen A, Bushart W, Steidinger J, Funk M, Hellner KA.
    Klin Monbl Augenheilkd; 1978 Feb; 172(6):831-42. PubMed ID: 692018
    [Abstract] [Full Text] [Related]

  • 5. Variation of phenotype in Charcot-Marie-Tooth disease.
    Baker RS, Upton AR.
    Neuropadiatrie; 1979 Aug; 10(3):290-5. PubMed ID: 583067
    [Abstract] [Full Text] [Related]

  • 6. Hereditary angioneurotic edema and Charcot-Marie-Tooth disease in the same family.
    Fernandez PG, Day JH, Simpson NE, Zachariah PK.
    Can Med Assoc J; 1978 Sep 09; 119(5):455-8. PubMed ID: 688147
    [Abstract] [Full Text] [Related]

  • 7. Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2.
    Züchner S, De Jonghe P, Jordanova A, Claeys KG, Guergueltcheva V, Cherninkova S, Hamilton SR, Van Stavern G, Krajewski KM, Stajich J, Tournev I, Verhoeven K, Langerhorst CT, de Visser M, Baas F, Bird T, Timmerman V, Shy M, Vance JM.
    Ann Neurol; 2006 Feb 09; 59(2):276-81. PubMed ID: 16437557
    [Abstract] [Full Text] [Related]

  • 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 09; 14(6):679-84. PubMed ID: 6651251
    [Abstract] [Full Text] [Related]

  • 9. Palmoplantar keratoderma and Charcot-Marie-Tooth disease.
    Rabbiosi G, Borroni G, Pinelli P, Cosi V.
    Arch Dermatol; 1980 Jul 09; 116(7):789-90. PubMed ID: 6446889
    [Abstract] [Full Text] [Related]

  • 10. Peroneal musclar atrophy (of Charcot-Marie-Tooth) in two African brothers.
    Billinghurst JR.
    Afr J Med Med Sci; 1976 Dec 09; 5(4):269-72. PubMed ID: 829740
    [Abstract] [Full Text] [Related]

  • 11. [Charcot-Marie amyotrophy associated with bilateral optic atrophy and diabetes].
    Giordano C, Bertrand E, Barabe P, Bizouard P.
    Med Trop (Mars); 1969 Dec 09; 29(6):720-4. PubMed ID: 5403110
    [No Abstract] [Full Text] [Related]

  • 12. [Autopsy case of Charcot-Marie-Tooth disease with optic nerve atrophy and degeneration of the spinal tract. A family with muscular atrophy, ataxia, retinal degeneration and diabetes mellitus].
    Oguchi K, Tsubaki T, Ikuta F.
    Rinsho Shinkeigaku; 1977 Jan 09; 17(1):52-7. PubMed ID: 557401
    [No Abstract] [Full Text] [Related]

  • 13. The clinical findings in Leber's hereditary optic neuroretinopathy. Leber's disease.
    Nikoskelainen E.
    Trans Ophthalmol Soc U K (1962); 1985 Jan 09; 104 ( Pt 8)():845-52. PubMed ID: 3879564
    [Abstract] [Full Text] [Related]

  • 14. 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 Jan 09; 27(3-4):177-89. PubMed ID: 6965173
    [Abstract] [Full Text] [Related]

  • 15. [Ocular findings in Charcot-Marie-Tooth disease, HMSN type I].
    Bürki E.
    Klin Monbl Augenheilkd; 1981 Aug 09; 179(2):94-6. PubMed ID: 7347789
    [Abstract] [Full Text] [Related]

  • 16. Malignant melanoma and Charcot-Marie-Tooth disease.
    Greene MH, Mead GD, Reimer RR, Bergfeld WF, Fraumeni JF.
    Am J Med Genet; 1980 Aug 09; 5(1):69-71. PubMed ID: 7395902
    [Abstract] [Full Text] [Related]

  • 17. [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 Aug 09; 30(2-3):222-8. PubMed ID: 6544478
    [No Abstract] [Full Text] [Related]

  • 18. [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]

  • 19. 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]

  • 20. [Leber's disease associated with myelinated fibers].
    Czechowicz-Janicka K, Iwaszkiewicz E.
    Klin Oczna; 1974 Feb 10; 44(2):173-7. PubMed ID: 4453100
    [No Abstract] [Full Text] [Related]

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