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Journal Abstract Search

149 related items for PubMed ID: 5173114

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

  • 2. [Polymorphism of Charcot-Marie-Tooth neural amyotrophy in uniovular twins].
    Popov'ian MD, Dubinskaia EE, Ageeva TS.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1977 Feb; 77(10):1446-8. PubMed ID: 563155
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. Recessive inheritance in a neuronal motor neuropathy form of peroneal muscular atrophy.
    Frajman M, Brilla E, Gutiérrez A, Hun L.
    Rev Invest Clin; 1983 Jan 05; 35(4):305-8. PubMed ID: 6672928
    [No Abstract] [Full Text] [Related]

  • 5. Variation of phenotype in Charcot-Marie-Tooth disease.
    Baker RS, Upton AR.
    Neuropadiatrie; 1979 Aug 05; 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. Charcot-Marie-Tooth disease with sensorineural hearing loss--an autosomal dominant trait.
    Kousseff BG, Hadro TA, Treiber DL, Wollner T, Morris C.
    Birth Defects Orig Artic Ser; 1982 Sep 09; 18(3B):223-8. PubMed ID: 7139106
    [No Abstract] [Full Text] [Related]

  • 8. A family with Charcot-Marie-Tooth disease and Leber's optic atrophy.
    McLeod JG, Low PA, Morgan JA.
    Proc Aust Assoc Neurol; 1975 Sep 09; 12():23-5. PubMed ID: 1215391
    [Abstract] [Full Text] [Related]

  • 9. [X-linked recessively inherited peroneal muscular atrophy].
    Wang DS.
    Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1989 Jun 09; 22(3):139-40, 190. PubMed ID: 2591266
    [Abstract] [Full Text] [Related]

  • 10. [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 Jun 09; 33(3):303-7. PubMed ID: 7330503
    [No Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. [A case of Charcot-Marie-Tooth muscular atrophy in monozygotic twins].
    Mrowiec W, Termińska-Mrowiec K.
    Wiad Lek; 1987 Sep 15; 40(18):1292-5. PubMed ID: 3445607
    [No Abstract] [Full Text] [Related]

  • 13. Hypertrophic interstitial neuropathy of Déjérine-Sottas.
    Beighton PH.
    Birth Defects Orig Artic Ser; 1971 Feb 15; 7(2):103-4. PubMed ID: 5173113
    [No Abstract] [Full Text] [Related]

  • 14. Autosomal recessive inheritance of Charcot-Marie-Tooth disease associated with sensorineural deafness.
    Cornell J, Sellars S, Beighton P.
    Clin Genet; 1984 Feb 15; 25(2):163-5. PubMed ID: 6705250
    [Abstract] [Full Text] [Related]

  • 15. [Charcot-Marie-Tooth disease. Genetical, clinical and electrodiagnostic study of 2 families].
    Krstić S, Vidaković Z, Ignjatović M.
    Srp Arh Celok Lek; 1975 Sep 15; 103(9):769-77. PubMed ID: 1228922
    [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 Sep 15; 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 Sep 15; 30(2-3):222-8. PubMed ID: 6544478
    [No Abstract] [Full Text] [Related]

  • 18. 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 15; 5(3):185-96. PubMed ID: 7088015
    [No Abstract] [Full Text] [Related]

  • 19. Pathogenesis of pes cavus in Charcot-Marie-Tooth disease.
    Sabir M, Lyttle D.
    Clin Orthop Relat Res; 1983 May 15; (175):173-8. PubMed ID: 6839584
    [Abstract] [Full Text] [Related]

  • 20. Sex-linked recessive inheritance in Charcot-Marie-tooth disease with partial clinical manifestations in female carriers.
    Fryns JP, Van den Berghe H.
    Hum Genet; 1980 May 15; 55(3):413-5. PubMed ID: 7203475
    [Abstract] [Full Text] [Related]

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