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Journal Abstract Search

138 related items for PubMed ID: 18376127

  • 1. Increased prevalence of significant recurrent headache in preclinical familial Alzheimer's disease mutation carriers.
    Ringman JM, Romano JD, Medina LD, Rodriguez-Agudelo Y, Schaffer B, Varpetian A, Ortiz F, Fitten LJ, Cummings JL, Baloh RW.
    Dement Geriatr Cogn Disord; 2008; 25(4):380-4. PubMed ID: 18376127
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  • 4. [Alzheimer's disease. Present and future role of genetics].
    Roks G.
    Tijdschr Gerontol Geriatr; 2003 Feb; 34(1):13-20. PubMed ID: 12629906
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  • 5. Presenilin-1 mutation E318G and familial Alzheimer's disease in the Italian population.
    Albani D, Roiter I, Artuso V, Batelli S, Prato F, Pesaresi M, Galimberti D, Scarpini E, Bruni A, Franceschi M, Piras MR, Confaloni A, Forloni G.
    Neurobiol Aging; 2007 Nov; 28(11):1682-8. PubMed ID: 16952411
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  • 9. Lifetime prevalence of migraine and other headaches lasting 4 or more hours: the Atherosclerosis Risk in Communities (ARIC) study.
    Carson AP, Rose KM, Sanford CP, Ephross SA, Stang PE, Hunt KJ, Brown CA, Szklo M.
    Headache; 2004 Jan; 44(1):20-8. PubMed ID: 14979879
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  • 10. No association of spastic paraparesis genes in PSEN1 Alzheimer's disease with spastic paraparesis.
    Karlstrom H, Kwok JB, Gregory GC, Hallupp M, Brooks WS, Schofield PR.
    Neuroreport; 2007 Aug 06; 18(12):1267-9. PubMed ID: 17632280
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  • 12. 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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  • 13. Advances in genetic testing for Alzheimer's disease.
    Howard KL, Filley CM.
    Rev Neurol Dis; 2009 May 15; 6(1):26-32. PubMed ID: 19367221
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  • 14. [Performance of carriers and non-carriers of the E280A mutation for familial Alzheimer's disease in a naming test].
    Tirado V, Muñoz C, Aguirre C, Pineda DA, Lopera F.
    Rev Neurol; 2009 May 15; 39(4):322-6. PubMed ID: 15340889
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  • 15. A presenilin 1 mutation (Arg278Ser) associated with early onset Alzheimer's disease and spastic paraparesis.
    Raman A, Lin X, Suri M, Hewitt M, Constantinescu CS, Phillips MF.
    J Neurol Sci; 2007 Sep 15; 260(1-2):78-82. PubMed ID: 17507029
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  • 18. A novel presenilin 1 mutation (Y154N) in a patient with early onset Alzheimer's disease with spastic paraparesis.
    Hattori S, Sakuma K, Wakutani Y, Wada K, Shimoda M, Urakami K, Kowa H, Nakashima K.
    Neurosci Lett; 2004 Sep 30; 368(3):319-22. PubMed ID: 15364419
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  • 20. Presenilin 1 polymorphism associated with Alzheimer's disease in apolipoprotein E4 carriers.
    Martínez-García A, Aldudo J, Recuero M, Sastre I, Vilella-Cuadrada E, Rosich-Estragó M, Frank A, Valdivieso F, Bullido MJ.
    Dement Geriatr Cogn Disord; 2008 Sep 30; 26(5):440-4. PubMed ID: 18957849
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