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Journal Abstract Search

671 related items for PubMed ID: 10441572

  • 1. 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; 65(3):664-70. PubMed ID: 10441572
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  • 3. Molecular diagnosis of autosomal dominant early onset Alzheimer's disease: an update.
    Raux G, Guyant-Maréchal L, Martin C, Bou J, Penet C, Brice A, Hannequin D, Frebourg T, Campion D.
    J Med Genet; 2005 Oct; 42(10):793-5. PubMed ID: 16033913
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  • 7. Seizures in dominantly inherited Alzheimer disease.
    Zarea A, Charbonnier C, Rovelet-Lecrux A, Nicolas G, Rousseau S, Borden A, Pariente J, Le Ber I, Pasquier F, Formaglio M, Martinaud O, Rollin-Sillaire A, Sarazin M, Croisile B, Boutoleau-Bretonnière C, Ceccaldi M, Gabelle A, Chamard L, Blanc F, Sellal F, Paquet C, Campion D, Hannequin D, Wallon D, PHRC GMAJ Collaborators.
    Neurology; 2016 Aug 30; 87(9):912-9. PubMed ID: 27466472
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  • 11. 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 30; 184(2):991-6. PubMed ID: 14769392
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  • 12. A novel mutation in the PSEN2 gene (T430M) associated with variable expression in a family with early-onset Alzheimer disease.
    Ezquerra M, Lleó A, Castellví M, Queralt R, Santacruz P, Pastor P, Molinuevo JL, Blesa R, Oliva R.
    Arch Neurol; 2003 Aug 30; 60(8):1149-51. PubMed ID: 12925374
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  • 13. Early-onset Alzheimer's disease in two Iranian families: a genetic study.
    Noroozian M, Azadfar P, Akbari L, Sadeghi A, Houshmand M, Vousooghi N, Zarrindast MR, Minagar A.
    Dement Geriatr Cogn Disord; 2014 Aug 30; 38(5-6):330-6. PubMed ID: 25138979
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  • 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 30; 35(8):1957.e1-6. PubMed ID: 24650794
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  • 16. Mutation profile of APP, PSEN1, and PSEN2 in Chinese familial Alzheimer's disease.
    Gao Y, Ren RJ, Zhong ZL, Dammer E, Zhao QH, Shan S, Zhou Z, Li X, Zhang YQ, Cui HL, Hu YB, Chen SD, Chen JJ, Guo QH, Wang G.
    Neurobiol Aging; 2019 May 30; 77():154-157. PubMed ID: 30822634
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  • 17. Clinical and genetic analysis of a Chilean family with early-onset autosomal dominant Alzheimer's disease.
    Sinning M, van Rooyen JP, Venegas-Francke P, Vásquez C, Behrens MI, Ramírez A.
    J Alzheimers Dis; 2010 May 30; 21(3):757-61. PubMed ID: 20571222
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  • 18. [Genetic counseling and testing for families with Alzheimer's disease].
    Kowalska A.
    Neurol Neurochir Pol; 2004 May 30; 38(6):495-501. PubMed ID: 15654674
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  • 19. Three-year follow-up of a patient with early-onset Alzheimer's disease with presenilin-2 N141I mutation - case report and review of the literature.
    Nikisch G, Hertel A, Kiessling B, Wagner T, Krasz D, Hofmann E, Wiedemann G.
    Eur J Med Res; 2008 Dec 03; 13(12):579-84. PubMed ID: 19073399
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