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

291 related items for PubMed ID: 14570818

  • 1. Novel presenilin 1 mutation with profound neurofibrillary pathology in an indigenous Southern African family with early-onset Alzheimer's disease.
    Heckmann JM, Low WC, de Villiers C, Rutherfoord S, Vorster A, Rao H, Morris CM, Ramesar RS, Kalaria RN.
    Brain; 2004 Jan; 127(Pt 1):133-42. PubMed ID: 14570818
    [Abstract] [Full Text] [Related]

  • 2. Novel presenilin 1 mutation (S170F) causing Alzheimer disease with Lewy bodies in the third decade of life.
    Snider BJ, Norton J, Coats MA, Chakraverty S, Hou CE, Jervis R, Lendon CL, Goate AM, McKeel DW, Morris JC.
    Arch Neurol; 2005 Dec; 62(12):1821-30. PubMed ID: 16344340
    [Abstract] [Full Text] [Related]

  • 3. Aberrant accentuation of neurofibrillary degeneration in the hippocampus of Alzheimer's disease with amyloid precursor protein 717 and presenilin-1 gene mutations.
    Sudo S, Shiozawa M, Cairns NJ, Wada Y.
    J Neurol Sci; 2005 Jul 15; 234(1-2):55-65. PubMed ID: 15946688
    [Abstract] [Full Text] [Related]

  • 4. NACP/alpha-synuclein, NAC, and beta-amyloid pathology of familial Alzheimer's disease with the E184D presenilin-1 mutation: a clinicopathological study of two autopsy cases.
    Yokota O, Terada S, Ishizu H, Ujike H, Ishihara T, Nakashima H, Yasuda M, Kitamura Y, Uéda K, Checler F, Kuroda S.
    Acta Neuropathol; 2002 Dec 15; 104(6):637-48. PubMed ID: 12410385
    [Abstract] [Full Text] [Related]

  • 5. E280A PS-1 mutation causes Alzheimer's disease but age of onset is not modified by ApoE alleles.
    Lendon CL, Martinez A, Behrens IM, Kosik KS, Madrigal L, Norton J, Neuman R, Myers A, Busfield F, Wragg M, Arcos M, Arango Viana JC, Ossa J, Ruiz A, Goate AM, Lopera F.
    Hum Mutat; 1997 Dec 15; 10(3):186-95. PubMed ID: 9298817
    [Abstract] [Full Text] [Related]

  • 6. A novel presenilin-1 mutation: increased beta-amyloid and neurofibrillary changes.
    Gómez-Isla T, Wasco W, Pettingell WP, Gurubhagavatula S, Schmidt SD, Jondro PD, McNamara M, Rodes LA, DiBlasi T, Growdon WB, Seubert P, Schenk D, Growdon JH, Hyman BT, Tanzi RE.
    Ann Neurol; 1997 Jun 15; 41(6):809-13. PubMed ID: 9189043
    [Abstract] [Full Text] [Related]

  • 7. Apolipoprotein Eepsilon4 modifies Alzheimer's disease onset in an E280A PS1 kindred.
    Pastor P, Roe CM, Villegas A, Bedoya G, Chakraverty S, García G, Tirado V, Norton J, Ríos S, Martínez M, Kosik KS, Lopera F, Goate AM.
    Ann Neurol; 2003 Aug 15; 54(2):163-9. PubMed ID: 12891668
    [Abstract] [Full Text] [Related]

  • 8. Cytoskeletal alterations differentiate presenilin-1 and sporadic Alzheimer's disease.
    Woodhouse A, Shepherd CE, Sokolova A, Carroll VL, King AE, Halliday GM, Dickson TC, Vickers JC.
    Acta Neuropathol; 2009 Jan 15; 117(1):19-29. PubMed ID: 19015863
    [Abstract] [Full Text] [Related]

  • 9. 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 15; 128(Pt 7):1707-15. PubMed ID: 15843424
    [Abstract] [Full Text] [Related]

  • 10. Molecular genetics of Alzheimer's disease: presenilin 1 gene analysis in a cohort of patients from the Poznań region.
    Kowalska A, Wender M, Florczak J, Pruchnik-Wolinska D, Modestowicz R, Szczech J, Rossa G, Kozubski W.
    J Appl Genet; 2003 Jul 15; 44(2):231-4. PubMed ID: 12817569
    [Abstract] [Full Text] [Related]

  • 11. [Genetic factors and a polygenic model of Alzheimer's disease].
    Rogaev EI.
    Genetika; 1999 Nov 15; 35(11):1558-71. PubMed ID: 10624576
    [Abstract] [Full Text] [Related]

  • 12. [Genetics of late-onset Alzheimer's disease: vascular risk and beta-amyloid metabolism].
    Panza F, Solfrizzi V, D'Introno A, Capurso C, Colacicco AM, Torres F, Altomare E, Capurso A.
    Recenti Prog Med; 2002 Sep 15; 93(9):489-97. PubMed ID: 12355988
    [Abstract] [Full Text] [Related]

  • 13. A novel mutation (G217D) in the Presenilin 1 gene ( PSEN1) in a Japanese family: presenile dementia and parkinsonism are associated with cotton wool plaques in the cortex and striatum.
    Takao M, Ghetti B, Hayakawa I, Ikeda E, Fukuuchi Y, Miravalle L, Piccardo P, Murrell JR, Glazier BS, Koto A.
    Acta Neuropathol; 2002 Aug 15; 104(2):155-70. PubMed ID: 12111359
    [Abstract] [Full Text] [Related]

  • 14. The clinical phenotype of two missense mutations in the presenilin I gene in Japanese patients.
    Ikeda M, Sharma V, Sumi SM, Rogaeva EA, Poorkaj P, Sherrington R, Nee L, Tsuda T, Oda N, Watanabe M, Aoki M, Shoji M, Abe K, Itoyama Y, Hirai S, Schellenberg GD, Bird TD, St George-Hyslop PH.
    Ann Neurol; 1996 Dec 15; 40(6):912-7. PubMed ID: 9007097
    [Abstract] [Full Text] [Related]

  • 15. Amyloid angiopathy in a Volga German family with Alzheimer's disease and a presenilin-2 mutation (N141I).
    Nochlin D, Bird TD, Nemens EJ, Ball MJ, Sumi SM.
    Ann Neurol; 1998 Jan 15; 43(1):131-5. PubMed ID: 9450781
    [Abstract] [Full Text] [Related]

  • 16. CA1 hippocampal neuronal loss in familial Alzheimer's disease presenilin-1 E280A mutation is related to epilepsy.
    Velez-Pardo C, Arellano JI, Cardona-Gomez P, Jimenez Del Rio M, Lopera F, De Felipe J.
    Epilepsia; 2004 Jul 15; 45(7):751-6. PubMed ID: 15230697
    [Abstract] [Full Text] [Related]

  • 17. [Etiology and genetics of Alzheimer disease].
    Myhre A, Tysnes OB.
    Tidsskr Nor Laegeforen; 2002 Jan 10; 122(1):50-3. PubMed ID: 11851296
    [Abstract] [Full Text] [Related]

  • 18. A polymorphism of the interleukin-1 beta gene at position +3953 influences progression and neuro-pathological hallmarks of Alzheimer's disease.
    Licastro F, Veglia F, Chiappelli M, Grimaldi LM, Masliah E.
    Neurobiol Aging; 2004 Sep 10; 25(8):1017-22. PubMed ID: 15212826
    [Abstract] [Full Text] [Related]

  • 19. [A Japanese family with familial Alzheimer's disease associated with presenilin 1 mutation: relationship between younger age of onset and ApoE gene polymorphism].
    Marui W, Iseki E, Sugiyama N, Matsumura T, Suzuki K, Odawara T, Hino H, Kosaka K.
    No To Shinkei; 2003 Apr 10; 55(4):349-53. PubMed ID: 12755040
    [Abstract] [Full Text] [Related]

  • 20. The effect of apolipoprotein E genotype on expression of an autosomal dominant schizophreniform disorder with progressive dementia and neurofibrillary tangles.
    Tsuang D, Raskind MA, Leverenz J, Peskind ER, Schellenberg G, Bird TD.
    Biol Psychiatry; 1997 Jan 15; 41(2):191-5. PubMed ID: 9018389
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 15.