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Journal Abstract Search

102 related items for PubMed ID: 1027118

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

  • 2. 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]

  • 3. 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]

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

  • 5. [Family with hereditary polyneuropthy assoicated with pyramidal signs].
    Doi H, Shibasaki H, Goto I, Kuroiwa Y, Ohta M.
    Rinsho Shinkeigaku; 1976 Sep 09; 16(9):642-8. PubMed ID: 1034548
    [No Abstract] [Full Text] [Related]

  • 6. Hypertrophic interstitial neuropathy of Déjérine-Sottas.
    Beighton PH.
    Birth Defects Orig Artic Ser; 1971 Feb 09; 7(2):103-4. PubMed ID: 5173113
    [No Abstract] [Full Text] [Related]

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

  • 8. [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]

  • 9. [Peroneal muscular atrophy associated with intellectual impairment and pyramidal signs].
    Sobue G, Ibi T, Matsuoka Y, Takahashi A.
    Rinsho Shinkeigaku; 1985 Jul 10; 25(7):818-25. PubMed ID: 4075646
    [No Abstract] [Full Text] [Related]

  • 10. [Report of 9 cases of hereditary neuromuscular atrophy and investigation of its genetic patterns].
    Li ZX.
    Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1983 Aug 10; 16(4):210-2. PubMed ID: 6641396
    [No Abstract] [Full Text] [Related]

  • 11. [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]

  • 12. 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 Oct 10; 27(3-4):177-89. PubMed ID: 6965173
    [Abstract] [Full Text] [Related]

  • 13. [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]

  • 14. Recessively inherited Charcot-Marie-Tooth syndrome in identical twins.
    Beighton PH.
    Birth Defects Orig Artic Ser; 1971 Feb 10; 7(2):105. PubMed ID: 5173114
    [No Abstract] [Full Text] [Related]

  • 15. 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 Feb 10; 18(3B):223-8. PubMed ID: 7139106
    [No Abstract] [Full Text] [Related]

  • 16. 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 10; 6(2):76-81. PubMed ID: 2942573
    [Abstract] [Full Text] [Related]

  • 17. [Charcot-Marie-Tooth disease. Genetical, clinical and electrodiagnostic study of 2 families].
    Krstić S, Vidaković Z, Ignjatović M.
    Srp Arh Celok Lek; 1975 Sep 10; 103(9):769-77. PubMed ID: 1228922
    [No Abstract] [Full Text] [Related]

  • 18. 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]

  • 19. [Hereditary spastic paraplegia associated with peroneal muscular atrophy].
    Laso FJ, Cacho J, Díez Jarilla JL, González Macías J.
    Med Clin (Barc); 1982 Apr 16; 78(8):329-31. PubMed ID: 7087602
    [No Abstract] [Full Text] [Related]

  • 20. Pathogenesis of Charcot-Marie-Tooth disease. Gait analysis and electrophysiologic, genetic, histopathologic, and enzyme studies in a kinship.
    Sabir M, Lyttle D.
    Clin Orthop Relat Res; 1984 Apr 16; (184):223-35. PubMed ID: 6705352
    [Abstract] [Full Text] [Related]

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