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Journal Abstract Search

159 related items for PubMed ID: 25138979

  • 1.
    ; . PubMed ID:
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  • 2. APP, PSEN1, and PSEN2 Mutations in Asian Patients with Early-Onset Alzheimer Disease.
    Giau VV, Bagyinszky E, Youn YC, An SSA, Kim S.
    Int J Mol Sci; 2019 Sep 25; 20(19):. PubMed ID: 31557888
    [Abstract] [Full Text] [Related]

  • 3. A genetic screen of the mutations in the Korean patients with early-onset Alzheimer's disease.
    An SS, Park SA, Bagyinszky E, Bae SO, Kim YJ, Im JY, Park KW, Park KH, Kim EJ, Jeong JH, Kim JH, Han HJ, Choi SH, Kim S.
    Clin Interv Aging; 2016 Sep 25; 11():1817-1822. PubMed ID: 28008242
    [Abstract] [Full Text] [Related]

  • 4. Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrum.
    Campion D, Dumanchin C, Hannequin D, Dubois B, Belliard S, Puel M, Thomas-Anterion C, Michon A, Martin C, Charbonnier F, Raux G, Camuzat A, Penet C, Mesnage V, Martinez M, Clerget-Darpoux F, Brice A, Frebourg T.
    Am J Hum Genet; 1999 Sep 25; 65(3):664-70. PubMed ID: 10441572
    [Abstract] [Full Text] [Related]

  • 5. APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic cases.
    Lanoiselée HM, Nicolas G, Wallon D, Rovelet-Lecrux A, Lacour M, Rousseau S, Richard AC, Pasquier F, Rollin-Sillaire A, Martinaud O, Quillard-Muraine M, de la Sayette V, Boutoleau-Bretonniere C, Etcharry-Bouyx F, Chauviré V, Sarazin M, le Ber I, Epelbaum S, Jonveaux T, Rouaud O, Ceccaldi M, Félician O, Godefroy O, Formaglio M, Croisile B, Auriacombe S, Chamard L, Vincent JL, Sauvée M, Marelli-Tosi C, Gabelle A, Ozsancak C, Pariente J, Paquet C, Hannequin D, Campion D, collaborators of the CNR-MAJ project.
    PLoS Med; 2017 Mar 25; 14(3):e1002270. PubMed ID: 28350801
    [Abstract] [Full Text] [Related]

  • 6. Genetic study of familial cases of Alzheimer's disease.
    Kowalska A, Pruchnik-Wolińska D, Florczak J, Modestowicz R, Szczech J, Kozubski W, Rossa G, Wender M.
    Acta Biochim Pol; 2004 Mar 25; 51(1):245-52. PubMed ID: 15094846
    [Abstract] [Full Text] [Related]

  • 7. Molecular Genetics of Early- and Late-Onset Alzheimer's Disease.
    Uddin MS, Hasana S, Hossain MF, Islam MS, Behl T, Perveen A, Hafeez A, Ashraf GM.
    Curr Gene Ther; 2021 Mar 25; 21(1):43-52. PubMed ID: 33231156
    [Abstract] [Full Text] [Related]

  • 8. Novel presenilin mutations within Moroccan patients with Early-Onset Alzheimer's Disease.
    El Kadmiri N, Zaid N, Zaid Y, Tadevosyan A, Hachem A, Dubé MP, Hamzi K, El Moutawakil B, Slassi I, Nadifi S.
    Neuroscience; 2014 Jun 06; 269():215-22. PubMed ID: 24704512
    [Abstract] [Full Text] [Related]

  • 9. Screening for Genetic Mutations Associated with Early-Onset Alzheimer's Disease in Han Chinese.
    Liu C, Cong L, Zhu M, Wang Y, Tang S, Han X, Zhang Q, Tian N, Liu K, Liang X, Fa W, Wang N, Hou T, Du Y.
    Curr Alzheimer Res; 2022 Jun 06; 19(10):724-733. PubMed ID: 36306459
    [Abstract] [Full Text] [Related]

  • 10. Exome sequencing identifies 2 novel presenilin 1 mutations (p.L166V and p.S230R) in British early-onset Alzheimer's disease.
    Sassi C, Guerreiro R, Gibbs R, Ding J, Lupton MK, Troakes C, Lunnon K, Al-Sarraj S, Brown KS, Medway C, Lord J, Turton J, Mann D, Snowden J, Neary D, Harris J, Bras J, ARUK Consortium, Morgan K, Powell JF, Singleton A, Hardy J.
    Neurobiol Aging; 2014 Oct 06; 35(10):2422.e13-6. PubMed ID: 24880964
    [Abstract] [Full Text] [Related]

  • 11. Molecular genetic analysis of the APP, PSEN1, and PSEN2 genes in Finnish patients with early-onset Alzheimer disease and frontotemporal lobar degeneration.
    Krüger J, Moilanen V, Majamaa K, Remes AM.
    Alzheimer Dis Assoc Disord; 2012 Oct 06; 26(3):272-6. PubMed ID: 21959359
    [Abstract] [Full Text] [Related]

  • 12. Double Mutations in a Patient with Early-Onset Alzheimer's Disease in Korea: An APP Val551Met and a PSEN2 His169Asn.
    Bae H, Shim KH, Yoo J, Yang YS, An SSA, Kang MJ.
    Int J Mol Sci; 2023 Apr 18; 24(8):. PubMed ID: 37108607
    [Abstract] [Full Text] [Related]

  • 13. Presenilin 1 and APP Gene Mutations in Early-Onset AD Families from a Southeast Region of China.
    Zhou J, Chen Y, Meng F, Zhang K, Liu X, Peng G.
    Curr Alzheimer Res; 2020 Apr 18; 17(6):540-546. PubMed ID: 32579498
    [Abstract] [Full Text] [Related]

  • 14. Genetic screening in early-onset Alzheimer's disease identified three novel presenilin mutations.
    Wong TH, Seelaar H, Melhem S, Rozemuller AJM, van Swieten JC.
    Neurobiol Aging; 2020 Feb 18; 86():201.e9-201.e14. PubMed ID: 30797548
    [Abstract] [Full Text] [Related]

  • 15. Gene mutations in a Han Chinese Alzheimer's disease cohort.
    Ma L, Zhang J, Shi Y, Wang W, Ren Z, Xia M, Zhang Y, Yang M.
    Brain Behav; 2019 Jan 18; 9(1):e01180. PubMed ID: 30549411
    [Abstract] [Full Text] [Related]

  • 16. 11C-PIB PET imaging reveals that amyloid deposition in cases with early-onset Alzheimer's disease in the absence of known mutations retains higher levels of PIB in the basal ganglia.
    Youn YC, Jang JW, Han SH, Kim H, Seok JW, Byun JS, Park KY, An SSA, Chun IK, Kim S.
    Clin Interv Aging; 2017 Jan 18; 12():1041-1048. PubMed ID: 28721032
    [Abstract] [Full Text] [Related]

  • 17. A Possible Pathogenic PSEN2 Gly56Ser Mutation in a Korean Patient with Early-Onset Alzheimer's Disease.
    Shim KH, Kang MJ, Bae H, Kim D, Park J, An SA, Jeong DE.
    Int J Mol Sci; 2022 Mar 09; 23(6):. PubMed ID: 35328387
    [Abstract] [Full Text] [Related]

  • 18. Clinical genetics of Alzheimer's disease.
    Zou Z, Liu C, Che C, Huang H.
    Biomed Res Int; 2014 Mar 09; 2014():291862. PubMed ID: 24955352
    [Abstract] [Full Text] [Related]

  • 19. Molecular genetics of early-onset Alzheimer's disease revisited.
    Cacace R, Sleegers K, Van Broeckhoven C.
    Alzheimers Dement; 2016 Jun 09; 12(6):733-48. PubMed ID: 27016693
    [Abstract] [Full Text] [Related]

  • 20. Association of Early-Onset Alzheimer Disease With Elevated Low-Density Lipoprotein Cholesterol Levels and Rare Genetic Coding Variants of APOB.
    Wingo TS, Cutler DJ, Wingo AP, Le NA, Rabinovici GD, Miller BL, Lah JJ, Levey AI.
    JAMA Neurol; 2019 Jul 01; 76(7):809-817. PubMed ID: 31135820
    [Abstract] [Full Text] [Related]

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