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5. Novel amyloid precursor protein gene mutation (codon 665Asp) in a patient with late-onset Alzheimer's disease. Peacock ML; Murman DL; Sima AA; Warren JT; Roses AD; Fink JK Ann Neurol; 1994 Apr; 35(4):432-8. PubMed ID: 8154870 [TBL] [Abstract][Full Text] [Related]
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8. 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; 418(3):282-5. PubMed ID: 17412506 [TBL] [Abstract][Full Text] [Related]
9. Cerebral amyloid angiopathy and dementia. Tian J; Shi J; Mann DM Panminerva Med; 2004 Dec; 46(4):253-64. PubMed ID: 15876981 [TBL] [Abstract][Full Text] [Related]
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11. APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy. Sleegers K; Brouwers N; Gijselinck I; Theuns J; Goossens D; Wauters J; Del-Favero J; Cruts M; van Duijn CM; Van Broeckhoven C Brain; 2006 Nov; 129(Pt 11):2977-83. PubMed ID: 16921174 [TBL] [Abstract][Full Text] [Related]
12. Apolipoprotein E epsilon4 allele frequency in elderly depressed patients with and without cerebrovascular disease. Traykov L; Bayle AC; Latour F; Lenoir H; Seux ML; Hanon O; Péquignot R; Bert P; Moulin F; Cantegreil I; Wenisch E; Batouche F; Mehrabian S; Rotrou Jd; Rigaud AS J Neurol Sci; 2007 Jun; 257(1-2):280-3. PubMed ID: 17337010 [TBL] [Abstract][Full Text] [Related]
13. Amyloid-β protein precursor gene expression in alzheimer's disease and other conditions. Pottier C; Wallon D; Lecrux AR; Maltete D; Bombois S; Jurici S; Frebourg T; Hannequin D; Campion D J Alzheimers Dis; 2012; 28(3):561-6. PubMed ID: 22045488 [TBL] [Abstract][Full Text] [Related]
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15. A novel mutation in the predicted TMIII domain of the PSEN2 gene in an Italian pedigree with atypical Alzheimer's disease. Piscopo P; Talarico G; Crestini A; Gasparini M; Malvezzi-Campeggi L; Piacentini E; Lenzi GL; Bruno G; Confaloni A J Alzheimers Dis; 2010; 20(1):43-7. PubMed ID: 20164579 [TBL] [Abstract][Full Text] [Related]
16. Phenotype associated with APP duplication in five families. Cabrejo L; Guyant-Maréchal L; Laquerrière A; Vercelletto M; De la Fournière F; Thomas-Antérion C; Verny C; Letournel F; Pasquier F; Vital A; Checler F; Frebourg T; Campion D; Hannequin D Brain; 2006 Nov; 129(Pt 11):2966-76. PubMed ID: 16959815 [TBL] [Abstract][Full Text] [Related]
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