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

Journal Abstract Search


114 related items for PubMed ID: 3157827

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 24. [Benign non-progressive familial chorea].
    Hirose G.
    Nihon Rinsho; 1993 Nov; 51(11):2968-71. PubMed ID: 8277578
    [Abstract] [Full Text] [Related]

  • 25.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 26. [Patients at the memory clinic with choreatic movements].
    Klompe LA, Eerenberg JG, Verschoor CJ.
    Tijdschr Gerontol Geriatr; 2011 Feb; 42(1):29-33. PubMed ID: 21400960
    [Abstract] [Full Text] [Related]

  • 27. [Diagnostic problems in different forms of Huntington chorea in children and adolescents].
    Michałowicz R, Karkowska B, Ignatowicz R, Kmieć T.
    Pol Tyg Lek; 1982 Nov 22; 37(45):1359-60. PubMed ID: 6219350
    [No Abstract] [Full Text] [Related]

  • 28.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 29. Benign familial chorea with onset in childhood.
    Chun RW, Daly RF, Mansheim BJ, Wolcott GJ.
    JAMA; 1973 Sep 24; 225(13):1603-7. PubMed ID: 4269386
    [No Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32. Predictive tests in Huntington's disease.
    Paulson GW.
    Res Publ Assoc Res Nerv Ment Dis; 1976 Sep 24; 55():317-29. PubMed ID: 137502
    [Abstract] [Full Text] [Related]

  • 33. [Huntington's disease].
    Heiberg A.
    Tidsskr Nor Laegeforen; 2008 Oct 09; 128(19):2214-7. PubMed ID: 18846148
    [Abstract] [Full Text] [Related]

  • 34. [DNA diagnosis of Huntington's chorea. Application and genetic counseling in 4 involved families].
    Hammer J, Mächler M, Schmid W.
    Schweiz Med Wochenschr; 1987 Dec 19; 117(51):2074-80. PubMed ID: 2963376
    [Abstract] [Full Text] [Related]

  • 35. Autosomal-dominant dentatorubropallidoluysian atrophy in the United Kingdom.
    Warner TT, Lennox GG, Janota I, Harding AE.
    Mov Disord; 1994 May 19; 9(3):289-96. PubMed ID: 8041369
    [Abstract] [Full Text] [Related]

  • 36. Huntington's disease in Thailand: a case report.
    Phanthumchinda K, Locharernkul C.
    J Med Assoc Thai; 1992 Feb 19; 75(2):123-6. PubMed ID: 1386618
    [Abstract] [Full Text] [Related]

  • 37.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 38. Benign (non-paroxysmal) familial chorea. Paediatric perspectives.
    Sleigh G, Lindenbaum RH.
    Arch Dis Child; 1981 Aug 19; 56(8):616-21. PubMed ID: 6455970
    [Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40. Diagnosis in Huntington disease.
    Gruenthal M, Olson WL.
    J Ky Med Assoc; 1994 Jul 19; 92(7):263-6. PubMed ID: 8064201
    [Abstract] [Full Text] [Related]


    Page: [Previous] [Next] [New Search]
    of 6.