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Journal Abstract Search

174 related items for PubMed ID: 18187157

  • 1. Atypical early-onset Alzheimer's disease caused by the Iranian APP mutation.
    Lindquist SG, Nielsen JE, Stokholm J, Schwartz M, Batbayli M, Ballegaard M, Erdal J, Krabbe K, Waldemar G.
    J Neurol Sci; 2008 May 15; 268(1-2):124-30. PubMed ID: 18187157
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  • 2. 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 15; 60(8):1149-51. PubMed ID: 12925374
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  • 8. Genetic risk and transcriptional variability of amyloid precursor protein in Alzheimer's disease.
    Brouwers N, Sleegers K, Engelborghs S, Bogaerts V, Serneels S, Kamali K, Corsmit E, De Leenheir E, Martin JJ, De Deyn PP, Van Broeckhoven C, Theuns J.
    Brain; 2006 Nov 15; 129(Pt 11):2984-91. PubMed ID: 16931535
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  • 9. [Alzheimer's disease. Present and future role of genetics].
    Roks G.
    Tijdschr Gerontol Geriatr; 2003 Feb 15; 34(1):13-20. PubMed ID: 12629906
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  • 13. 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 15; 62(12):1821-30. PubMed ID: 16344340
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  • 18. 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 15; 35(8):1957.e1-6. PubMed ID: 24650794
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  • 19. Molecular genetics of Alzheimer's disease: what have we learned?
    Van Gassen G, Van Broeckhoven C.
    Acta Neurol Belg; 2000 Jun 15; 100(2):65-76. PubMed ID: 10934557
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