These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

263 related items for PubMed ID: 6672928

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [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; 30(2-3):222-8. PubMed ID: 6544478
    [No Abstract] [Full Text] [Related]

  • 8. 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]

  • 9.
    ; . PubMed ID:
    [No 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 Feb; 33(3):303-7. PubMed ID: 7330503
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. [Peroneal muscular atrophy associated with intellectual impairment and pyramidal signs].
    Sobue G, Ibi T, Matsuoka Y, Takahashi A.
    Rinsho Shinkeigaku; 1985 Jul 09; 25(7):818-25. PubMed ID: 4075646
    [No Abstract] [Full Text] [Related]

  • 15. Peroneal muscular atrophy (Charcot-Marie-Tooth disease): a review of three cases.
    Turton RL, McCracken JW.
    J Am Osteopath Assoc; 1970 Oct 09; 70(2):138-45. PubMed ID: 5202533
    [No Abstract] [Full Text] [Related]

  • 16. [Hereditary motor and sensory neuropathy associated with retinitis pigmentosa and neural deafness].
    Murakami K, Sobue G, Takahashi A, Mitsuma T.
    Rinsho Shinkeigaku; 1986 Sep 09; 26(9):952-9. PubMed ID: 3791775
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Homozygous expression of a dominant gene for Charcot-Marie-Tooth neuropathy.
    Killian JM, Kloepfer HW.
    Ann Neurol; 1979 Jun 09; 5(6):515-22. PubMed ID: 475348
    [Abstract] [Full Text] [Related]

  • 19. [Charcot-Marie-Tooth disease. Genetical, clinical and electrodiagnostic study of 2 families].
    Krstić S, Vidaković Z, Ignjatović M.
    Srp Arh Celok Lek; 1975 Sep 09; 103(9):769-77. PubMed ID: 1228922
    [No Abstract] [Full Text] [Related]

  • 20. Serum enzymes in peroneal muscular atrophy (Charcot-Marie-Tooth disease).
    Switala KJ, Robinson N, Sances A, Larson S, Evans SM, Pintar K.
    Wis Med J; 1977 Jan 09; 76(1):S4-6. PubMed ID: 835307
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 14.