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648 related items for PubMed ID: 24704512

  • 1. 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]

  • 2. 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 Jun 06; 44(2):231-4. PubMed ID: 12817569
    [Abstract] [Full Text] [Related]

  • 3. Novel mutations in the amyloid precursor protein gene within Moroccan patients with Alzheimer's disease.
    El Kadmiri N, Zaid N, Hachem A, Zaid Y, Dubé MP, Hamzi K, El Moutawakil B, Slassi I, Nadifi S.
    J Mol Neurosci; 2014 Jun 06; 53(2):189-95. PubMed ID: 24627227
    [Abstract] [Full Text] [Related]

  • 4. [Clinical presentation of Moroccan cases with Alzheimer's disease].
    El Kadmiri N, Zaid Y, Hamzi K, Nadifi S, Slassi I, El Moutawakil B.
    Encephale; 2014 Dec 06; 40(6):481-6. PubMed ID: 25127896
    [Abstract] [Full Text] [Related]

  • 5. Brain expression of presenilins in sporadic and early-onset, familial Alzheimer's disease.
    Mathews PM, Cataldo AM, Kao BH, Rudnicki AG, Qin X, Yang JL, Jiang Y, Picciano M, Hulette C, Lippa CF, Bird TD, Nochlin D, Walter J, Haass C, Lévesque L, Fraser PE, Andreadis A, Nixon RA.
    Mol Med; 2000 Oct 06; 6(10):878-91. PubMed ID: 11126202
    [Abstract] [Full Text] [Related]

  • 6. The R269H mutation in presenilin-1 presenting as late-onset autosomal dominant Alzheimer's disease.
    Larner AJ, Ray PS, Doran M.
    J Neurol Sci; 2007 Jan 31; 252(2):173-6. PubMed ID: 17188713
    [Abstract] [Full Text] [Related]

  • 7. 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 31; 127(Pt 1):133-42. PubMed ID: 14570818
    [Abstract] [Full Text] [Related]

  • 8. 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 Jan 31; 11():1817-1822. PubMed ID: 28008242
    [Abstract] [Full Text] [Related]

  • 9. Presenilin-1 protein expression in familial and sporadic Alzheimer's disease.
    Levey AI, Heilman CJ, Lah JJ, Nash NR, Rees HD, Wakai M, Mirra SS, Rye DB, Nochlin D, Bird TD, Mufson EJ.
    Ann Neurol; 1997 Jun 31; 41(6):742-53. PubMed ID: 9189035
    [Abstract] [Full Text] [Related]

  • 10. Mutations in presenilin 1, presenilin 2 and amyloid precursor protein genes in patients with early-onset Alzheimer's disease in Poland.
    Zekanowski C, Styczyńska M, Pepłońska B, Gabryelewicz T, Religa D, Ilkowski J, Kijanowska-Haładyna B, Kotapka-Minc S, Mikkelsen S, Pfeffer A, Barczak A, Łuczywek E, Wasiak B, Chodakowska-Zebrowska M, Gustaw K, Łaczkowski J, Sobów T, Kuźnicki J, Barcikowska M.
    Exp Neurol; 2003 Dec 31; 184(2):991-6. PubMed ID: 14769392
    [Abstract] [Full Text] [Related]

  • 11. 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 31; 62(12):1821-30. PubMed ID: 16344340
    [Abstract] [Full Text] [Related]

  • 12. Presenilin 1 mutations in Polish families with early-onset Alzheimer's disease.
    Kowalska A, Pruchnik-Wolińska D, Florczak J, Szczech J, Kozubski W, Rossa G, Wender M.
    Folia Neuropathol; 2004 Dec 31; 42(1):9-14. PubMed ID: 15119739
    [Abstract] [Full Text] [Related]

  • 13. 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 Dec 31; 51(1):245-52. PubMed ID: 15094846
    [Abstract] [Full Text] [Related]

  • 14. Early-onset familial Alzheimer's disease (EOFAD).
    Wu L, Rosa-Neto P, Hsiung GY, Sadovnick AD, Masellis M, Black SE, Jia J, Gauthier S.
    Can J Neurol Sci; 2012 Jul 31; 39(4):436-45. PubMed ID: 22728850
    [Abstract] [Full Text] [Related]

  • 15. Mutational analysis in early-onset familial Alzheimer's disease in Mainland China.
    Jiao B, Tang B, Liu X, Xu J, Wang Y, Zhou L, Zhang F, Yan X, Zhou Y, Shen L.
    Neurobiol Aging; 2014 Aug 31; 35(8):1957.e1-6. PubMed ID: 24650794
    [Abstract] [Full Text] [Related]

  • 16. 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 31; 14(3):e1002270. PubMed ID: 28350801
    [Abstract] [Full Text] [Related]

  • 17. Phenotypic profile of early-onset familial Alzheimer's disease caused by presenilin-1 E280A mutation.
    Sepulveda-Falla D, Glatzel M, Lopera F.
    J Alzheimers Dis; 2012 Mar 31; 32(1):1-12. PubMed ID: 22766738
    [Abstract] [Full Text] [Related]

  • 18. Amyloid precursor protein gene analysis in familial Alzheimer's disease cases: a lack of mutations in exons 16 and 17.
    Kowalska A, Pruchnik-Wolińska D, Florczak J, Szczech J, Kozubski W, Rossa G, Wender M.
    Folia Neuropathol; 2004 Mar 31; 42(1):1-7. PubMed ID: 15119738
    [Abstract] [Full Text] [Related]

  • 19. [Genetic factors and a polygenic model of Alzheimer's disease].
    Rogaev EI.
    Genetika; 1999 Nov 31; 35(11):1558-71. PubMed ID: 10624576
    [Abstract] [Full Text] [Related]

  • 20. A mutation screening by DHPLC of PSEN1 and APP genes reveals no significant variation associated with the sporadic late-onset form of Alzheimer's disease.
    Scacchi R, Gambina G, Moretto G, Corbo RM.
    Neurosci Lett; 2007 May 18; 418(3):282-5. PubMed ID: 17412506
    [Abstract] [Full Text] [Related]

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