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Journal Abstract Search


125 related items for PubMed ID: 2173372

  • 41. Parkinson's disease and dementia with Lewy bodies: one disease or two?
    Richard IH, Papka M, Rubio A, Kurlan R.
    Mov Disord; 2002 Nov; 17(6):1161-5. PubMed ID: 12465052
    [Abstract] [Full Text] [Related]

  • 42. A Drosophila model of Parkinson's disease.
    Feany MB, Bender WW.
    Nature; 2000 Mar 23; 404(6776):394-8. PubMed ID: 10746727
    [Abstract] [Full Text] [Related]

  • 43. The relevance of the Lewy body to the pathogenesis of idiopathic Parkinson's disease.
    Gibb WR, Lees AJ.
    J Neurol Neurosurg Psychiatry; 1988 Jun 23; 51(6):745-52. PubMed ID: 2841426
    [Abstract] [Full Text] [Related]

  • 44. Pfeiffer acrocephalosyndactyly syndrome in mother and son with cloverleaf skull anomaly in the child.
    Soekarman D, Fryns JP, van den Berghe H.
    Genet Couns; 1992 Jun 23; 3(4):217-20. PubMed ID: 1472357
    [Abstract] [Full Text] [Related]

  • 45. [You make the diagnosis. Marshall syndrome].
    Freude S, Kozel-Lachmann D.
    Padiatr Padol; 1991 Jun 23; 26(4):197-8. PubMed ID: 1749629
    [No Abstract] [Full Text] [Related]

  • 46. Familial distal dysautonomia.
    Robinson B, Johnson R, Abernethy D, Holloway L.
    J Neurol Neurosurg Psychiatry; 1989 Nov 23; 52(11):1281-5. PubMed ID: 2592970
    [Abstract] [Full Text] [Related]

  • 47. Familial Alzheimer disease: a large, multigeneration German kindred.
    Frommelt P, Schnabel R, Kühne W, Nee LE, Polinsky RJ.
    Alzheimer Dis Assoc Disord; 1991 Nov 23; 5(1):36-43. PubMed ID: 2025423
    [Abstract] [Full Text] [Related]

  • 48. Autosomal dominant late-onset leukoencephalopathy. Clinical report of a new Italian family.
    Quattrocolo G, Leombruni S, Vaula G, Bergui M, Riva A, Bradac GB, Bergamini L.
    Eur Neurol; 1997 Nov 23; 37(1):53-61. PubMed ID: 9018034
    [Abstract] [Full Text] [Related]

  • 49. Genetics of Alzheimer's disease.
    Folstein MF, Warren A.
    Res Publ Assoc Res Nerv Ment Dis; 1991 Nov 23; 69():129-36. PubMed ID: 2003156
    [No Abstract] [Full Text] [Related]

  • 50. Clinical features of familial diffuse Lewy body disease.
    Ishikawa A, Takahashi H, Tanaka H, Hayashi T, Tsuji S.
    Eur Neurol; 1997 Nov 23; 38 Suppl 1():34-8. PubMed ID: 9276199
    [Abstract] [Full Text] [Related]

  • 51. Autosomal dominant inherited ventricular tachycardia.
    Rubin DA, O'Keefe A, Kay RH, McAllister A, Mendelson DM.
    Am Heart J; 1992 Apr 23; 123(4 Pt 1):1082-4. PubMed ID: 1549981
    [No Abstract] [Full Text] [Related]

  • 52. A family with multiple instances of definite, probable and possible early-onset Alzheimer's disease.
    Karlinsky H, Madrick E, Ridgley J, Berg JM, Becker R, Bergeron C, Hodgkinson S, Percy ME, McLachlan D.
    Br J Psychiatry; 1991 Oct 23; 159():524-30. PubMed ID: 1751863
    [Abstract] [Full Text] [Related]

  • 53. Genetic epidemiology of Parkinson's disease.
    Payami H, Zareparsi S.
    J Geriatr Psychiatry Neurol; 1998 Oct 23; 11(2):98-106. PubMed ID: 9877530
    [Abstract] [Full Text] [Related]

  • 54. An unusual presentation of Huntington's disease.
    Rivkin PR, Pearlson GD.
    Psychosomatics; 1998 Oct 23; 39(3):291-4. PubMed ID: 9664778
    [No Abstract] [Full Text] [Related]

  • 55. Two large British kindreds with familial Parkinson's disease: a clinico-pathological and genetic study.
    Nicholl DJ, Vaughan JR, Khan NL, Ho SL, Aldous DE, Lincoln S, Farrer M, Gayton JD, Davis MB, Piccini P, Daniel SE, Lennox GG, Brooks DJ, Williams AC, Wood NW.
    Brain; 2002 Jan 23; 125(Pt 1):44-57. PubMed ID: 11834592
    [Abstract] [Full Text] [Related]

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  • 59. [A case of idiopathic parkinsonism with many Lewy bodies in the cerebral cortex (author's transl)].
    Yoshimura T, Kato H, Ikeda K, Yashiki T, Kaiya H.
    Rinsho Shinkeigaku; 1977 Jul 23; 17(7):425-30. PubMed ID: 199390
    [No Abstract] [Full Text] [Related]

  • 60. Further evidence for genetic heterogeneity of autosomal dominant disorders with accumulation of multiple deletions of mitochondrial DNA.
    van Goethem G, Löfgren A, Martin JJ, van Broeckhoven C.
    J Med Genet; 2000 Jul 23; 37(7):547-8. PubMed ID: 10970191
    [No Abstract] [Full Text] [Related]


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