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Journal Abstract Search

156 related items for PubMed ID: 14475031

  • 1. Familial occurrence of neural muscle atrophy (Tooth-Marie-Charcot) combined with cerebral atrophy and parkinsonism.
    MOFFIE D.
    Psychiatr Neurol Neurochir; 1961; 64():381-91. PubMed ID: 14475031
    [No Abstract] [Full Text] [Related]

  • 2. Charcot-Marie-Tooth disease with associated myopathy. A report of a family.
    LUCAS GJ, FORSTER FM.
    Neurology; 1962 Sep; 12():629-36. PubMed ID: 14467082
    [No Abstract] [Full Text] [Related]

  • 3. [Charcot-Marie-Tooth amyotrophy in 2 brothers].
    MORETTI GF, STAEFFEN J, LORRAIN J, ROUX M, ROUSSEAU J.
    J Med Bord; 1961 Nov; 138():1440-8. PubMed ID: 14475928
    [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 Nov; 12():23-5. PubMed ID: 1215391
    [Abstract] [Full Text] [Related]

  • 5. [Brothers affected by the Charcot-Marie-Tooth peroneal muscular atrophy with a positive variant of the anticipation phenomenon].
    Gonçalves A, da Salva JB.
    Arq Neuropsiquiatr; 1977 Jun; 35(2):167-71. PubMed ID: 869740
    [Abstract] [Full Text] [Related]

  • 6. [Observations on three cases of Charcot-Marie-Tooth disease found among brothers].
    UEMURA N, IDA M.
    No To Shinkei; 1962 Jun; 14():505-11. PubMed ID: 13923525
    [No Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. Conduction velocity of nerves in a family with Charcot-Marie-Tooth disease: detection of latent involvement.
    DYCK PJ, LAMBERTEH, MULDER DW.
    Trans Am Neurol Assoc; 1961 Dec; 86():207-8. PubMed ID: 13888818
    [No Abstract] [Full Text] [Related]

  • 9. Linkage relations of locus for X-borne type of Charcot-Marie-Tooth muscular atrophy and that for Xg blood groups.
    de Weerdt CJ.
    J Med Genet; 1976 Oct; 13(5):399. PubMed ID: 1003451
    [Abstract] [Full Text] [Related]

  • 10. Progressive neuropathic (peroneal) muscular atrophy (Charcot-Marie-Tooth disease); histological findings in muscle biopsy specimens in fourteen cases, with notes on clinical diagnosis and familial occurrence.
    BRODAL A, BOYESEN S, FROVIG AG.
    AMA Arch Neurol Psychiatry; 1953 Jul; 70(1):1-29. PubMed ID: 13057401
    [No Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. Should Charcot-Marie-Tooth disease be genetically subgrouped on motor conduction velocity.
    Salisachs P, Findley LJ, Codina M, Martinez-Lage JM.
    J Neurol Neurosurg Psychiatry; 1982 Feb; 45(2):182-4. PubMed ID: 7069437
    [No Abstract] [Full Text] [Related]

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

  • 14. Charcot-Marie-Tooth disease and schizophrenia in identical twins.
    Manyam NV, Cowell HR, Katz L.
    JAMA; 1979 Jan 05; 241(1):54-5. PubMed ID: 569219
    [Abstract] [Full Text] [Related]

  • 15. Charcot-Marie-Tooth disease.
    Heimans JJ, Lindhout D.
    J Med Genet; 1983 Feb 05; 20(1):77-8. PubMed ID: 6842540
    [No 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 Feb 05; 5(1):69-71. PubMed ID: 7395902
    [Abstract] [Full Text] [Related]

  • 17. [Progressive neural muscular atrophy (amyotrophy of Charcot-Marie-Tooth)].
    STOJILJKOVIC S, ROKNIC M.
    Med Glas; 1961 Feb 05; 15():335-6. PubMed ID: 13917368
    [No Abstract] [Full Text] [Related]

  • 18. [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 05; 17(1):52-7. PubMed ID: 557401
    [No Abstract] [Full Text] [Related]

  • 19. 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]

  • 20. Recessively inherited Charcot-Marie-Tooth syndrome in identical twins.
    Beighton PH.
    Birth Defects Orig Artic Ser; 1971 Feb 09; 7(2):105. PubMed ID: 5173114
    [No Abstract] [Full Text] [Related]

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