HuGE Literature Finder
Records 1-13
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Association of Early-Onset Alzheimer Disease With Elevated Low-Density Lipoprotein Cholesterol Levels and Rare Genetic Coding Variants of APOB.
JAMA neurology 2019 May . Wingo Thomas S, Cutler David J, Wingo Aliza P, Le Ngoc-Anh, Rabinovici Gil D, Miller Bruce L, Lah James J, Levey Allan |
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Mutation profile of APP, PSEN1, and PSEN2 in Chinese familial Alzheimer's disease.
Neurobiology of aging 2019 Jan 77 154-157. Gao Ying, Ren Ru-Jing, Zhong Zi-Lin, Dammer Eric, Zhao Qian-Hua, Shan Shan, Zhou Zheng, Li Xia, Zhang Yue-Qi, Cui Hai-Lun, Hu Yong-Bo, Chen Sheng-Di, Chen Jian-Jun, Guo Qi-Hao, Wang Ga |
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Pleiotropic Effects of Variants in Dementia Genes in Parkinson Disease.
Frontiers in neuroscience 2018 12 230. Ibanez Laura, Dube Umber, Davis Albert A, Fernandez Maria V, Budde John, Cooper Breanna, Diez-Fairen Monica, Ortega-Cubero Sara, Pastor Pau, Perlmutter Joel S, Cruchaga Carlos, Benitez Bruno |
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Early-Onset Alzheimer Disease and Candidate Risk Genes Involved in Endolysosomal Transport.
JAMA neurology 2017 Jul . Kunkle Brian W, Vardarajan Badri N, Naj Adam C, Whitehead Patrice L, Rolati Sophie, Slifer Susan, Carney Regina M, Cuccaro Michael L, Vance Jeffery M, Gilbert John R, Wang Li-San, Farrer Lindsay A, Reitz Christiane, Haines Jonathan L, Beecham Gary W, Martin Eden R, Schellenberg Gerard D, Mayeux Richard P, Pericak-Vance Margaret |
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Seizures in dominantly inherited Alzheimer disease.
Neurology 2016 Aug 87 (9): 912-9. Zarea Aline, Charbonnier Camille, Rovelet-Lecrux Anne, Nicolas Gaël, Rousseau Stéphane, Borden Alaina, Pariente Jeremie, Le Ber Isabelle, Pasquier Florence, Formaglio Maite, Martinaud Olivier, Rollin-Sillaire Adeline, Sarazin Marie, Croisile Bernard, Boutoleau-Bretonnière Claire, Ceccaldi Mathieu, Gabelle Audrey, Chamard Ludivine, Blanc Frédéric, Sellal François, Paquet Claire, Campion Dominique, Hannequin Didier, Wallon David, |
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Dura mater is a potential source of Aß seeds.
Acta neuropathologica 2016 Mar . Kovacs Gabor G, Lutz Mirjam I, Ricken Gerda, Ströbel Thomas, Höftberger Romana, Preusser Matthias, Regelsberger Günther, Hönigschnabl Selma, Reiner Angelika, Fischer Peter, Budka Herbert, Hainfellner Johannes |
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C9ORF72 repeat expansions and other FTD gene mutations in a clinical AD patient series from Mayo Clinic.
American journal of neurodegenerative disease 2012 1 (1): 1. Wojtas A, Heggeli KA, Finch N, Baker M, Dejesus-Hernandez M, Younkin SG, Dickson DW, Graff-Radford NR, Rademakers R |
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High striatal amyloid beta-peptide deposition across different autosomal Alzheimer disease mutation types.
Archives of neurology 2009 Dec 66 (12): 1537-44. Villemagne Victor L, Ataka Suzuka, Mizuno Toshiki, Brooks William S, Wada Yasuhiro, Kondo Masaki, Jones Gareth, Watanabe Yasuyoshi, Mulligan Rachel, Nakagawa Masanori, Miki Takami, Shimada Hiroyuki, O'Keefe Graeme J, Masters Colin L, Mori Hiroshi, Rowe Christopher |
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A novel mutation in the PSEN2 gene (T430M) associated with variable expression in a family with early-onset Alzheimer disease.
Archives of neurology 2003 Aug 60 (8): 1149-51. Ezquerra Mario, Lleó Alberto, Castellví Magda, Queralt Rosa, Santacruz Pilar, Pastor Pau, Molinuevo José Luis, Blesa Rafael, Oliva Rafa |
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Evaluation of multiple presenilin 2 SNPs for association with early-onset sporadic Alzheimer disease.
American journal of medical genetics 2002 Aug 111 (2): 157-63. Howell W Mathias, Brookes Anthony |
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Regulatory region variability in the human presenilin-2 (PSEN2) gene: potential contribution to the gene activity and risk for AD.
Molecular psychiatry 2002 7 (8): 891-8. Riazanskaia N, Lukiw W J, Grigorenko A, Korovaitseva G, Dvoryanchikov G, Moliaka Y, Nicolaou M, Farrer L, Bazan N G, Rogaev |
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Systematic genetic study of Alzheimer disease in Latin America: mutation frequencies of the amyloid beta precursor protein and presenilin genes in Colombia.
American journal of medical genetics 2001 Oct 103 (2): 138-43. Arango D, Cruts M, Torres O, Backhovens H, Serrano M L, Villareal E, Montañes P, Matallana D, Cano C, Van Broeckhoven C, Jacquier |
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Molecular genetic analysis of the APP, PSEN1, and PSEN2 genes in Finnish patients with early-onset Alzheimer disease and frontotemporal lobar degeneration.
Alzheimer disease and associated disorders 0 26 (3): 272-6. Krüger Johanna, Moilanen Virpi, Majamaa Kari, Remes Anne |
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- Page last updated:Jul 01, 2021
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