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Journal Abstract Search

463 related items for PubMed ID: 17632280

  • 1. 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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  • 9. The novel PSEN1 M84V mutation associated to frontal dysexecutive syndrome, spastic paraparesis, and cerebellar atrophy in a dominant Alzheimer's disease family.
    Gallo M, Frangipane F, Cupidi C, De Bartolo M, Turone S, Ferrari C, Nacmias B, Grimaldi G, Laganà V, Colao R, Bernardi L, Anfossi M, Conidi ME, Vasso F, Curcio SAM, Mirabelli M, Smirne N, Torchia G, Muraca MG, Puccio G, Di Lorenzo R, Piccininni M, Tedde A, Maletta RG, Sorbi S, Bruni AC.
    Neurobiol Aging; 2017 Aug 06; 56():213.e7-213.e12. PubMed ID: 28532646
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  • 11. A novel presenilin 1 mutation (Ser169del) in a Chinese family with early-onset Alzheimer's disease.
    Guo J, Wei J, Liao S, Wang L, Jiang H, Tang B.
    Neurosci Lett; 2010 Jan 01; 468(1):34-7. PubMed ID: 19853643
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  • 14. PSEN1 polymorphisms alter the rate of cognitive decline in sporadic Alzheimer's disease patients.
    Belbin O, Beaumont H, Warden D, Smith AD, Kalsheker N, Morgan K.
    Neurobiol Aging; 2009 Dec 01; 30(12):1992-9. PubMed ID: 18403054
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  • 17. Presenilin-1 mutations in Alzheimer's disease: an update on genotype-phenotype relationships.
    Larner AJ.
    J Alzheimers Dis; 2013 Dec 01; 37(4):653-9. PubMed ID: 23948899
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  • 18. Genotype-phenotype analysis in early-onset Alzheimer's disease due to presenilin-1 mutations at codon 139.
    Hanisch F, Kölmel HW.
    Eur J Med Res; 2004 Jul 30; 9(7):361-4. PubMed ID: 15337637
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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 Jul 30; 26(5):440-4. PubMed ID: 18957849
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