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

176 related items for PubMed ID: 8291565

  • 21. Familial Alzheimer's disease: site of mutation influences clinical phenotype.
    Lippa CF, Swearer JM, Kane KJ, Nochlin D, Bird TD, Ghetti B, Nee LE, St George-Hyslop P, Pollen DA, Drachman DA.
    Ann Neurol; 2000 Sep; 48(3):376-9. PubMed ID: 10976645
    [Abstract] [Full Text] [Related]

  • 22. Linkage of familial Alzheimer disease to chromosome 14 in two large early-onset pedigrees: effects of marker allele frequencies on lod scores.
    Nechiporuk A, Fain P, Kort E, Nee LE, Frommelt E, Polinsky RJ, Korenberg JR, Pulst SM.
    Am J Med Genet; 1993 May 01; 48(1):63-6. PubMed ID: 8357039
    [Abstract] [Full Text] [Related]

  • 23. Two new approaches toward linkage heterogeneity of FAD: two-locus models and age of onset as a discriminator.
    Mérette C, Lehner T, Ott J.
    Genet Epidemiol; 1993 May 01; 10(6):455-9. PubMed ID: 8314043
    [Abstract] [Full Text] [Related]

  • 24. Chromosome 14-encoded Alzheimer's disease: genetic and clinicopathological description.
    Haltia M, Viitanen M, Sulkava R, Ala-Hurula V, Poyhonen M, Goldfarb L, Brown P, Levy E, Houlden H, Crook R.
    Ann Neurol; 1994 Sep 01; 36(3):362-7. PubMed ID: 8080244
    [Abstract] [Full Text] [Related]

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

  • 26. Alzheimer's disease aetiology: amyloid and chromosome 14.
    Houlden H, Mullan M.
    Br J Hosp Med; 1994 Sep 01; 49(8):535-6. PubMed ID: 8508237
    [No Abstract] [Full Text] [Related]

  • 27. A two-locus model for familial Alzheimer's disease?
    Macciardi F, Cavallini MC.
    Genet Epidemiol; 1993 Sep 01; 10(6):437-41. PubMed ID: 8314040
    [Abstract] [Full Text] [Related]

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

  • 29. A multigenerational pedigree of late-onset Alzheimer's disease implies new genetic causes.
    Jimenez-Escrig A, Gomez-Tortosa E, Baron M, Rabano A, Arcos-Burgos M, Palacios LG, Yusta A, Anta P, Perez I, Hierro M, Munoz DG, Barquero S.
    Brain; 2005 Jul 01; 128(Pt 7):1707-15. PubMed ID: 15843424
    [Abstract] [Full Text] [Related]

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

  • 31. Low prevalence of APP duplications in Swedish and Finnish patients with early-onset Alzheimer's disease.
    Blom ES, Viswanathan J, Kilander L, Helisalmi S, Soininen H, Lannfelt L, Ingelsson M, Glaser A, Hiltunen M.
    Eur J Hum Genet; 2008 Feb 01; 16(2):171-5. PubMed ID: 18043715
    [Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 37. The Seattle Alzheimer's disease data set.
    Wijsman EM, Bird TD, Martin GM, Schellenberg GD.
    Genet Epidemiol; 1993 Feb 01; 10(6):365-9. PubMed ID: 8314028
    [Abstract] [Full Text] [Related]

  • 38. [Dominant forms of Alzheimer's disease: from genotype to phenotype].
    Hannequin D, Campion D.
    Rev Neurol (Paris); 2001 Apr 01; 157(4):384-92. PubMed ID: 11398010
    [Abstract] [Full Text] [Related]

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

  • 40. Familial clustering and genetic risk for dementia in a genetically isolated Dutch population.
    Sleegers K, Roks G, Theuns J, Aulchenko YS, Rademakers R, Cruts M, van Gool WA, Van Broeckhoven C, Heutink P, Oostra BA, van Swieten JC, van Duijn CM.
    Brain; 2004 Jul 01; 127(Pt 7):1641-9. PubMed ID: 15130954
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 9.