Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Alzheimer Disease and LRRK2[original query] |
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LRRK2 p.G2019S mutation is not common among Alzheimer's disease patients in Brazil. Disease markers 2009 27 (1): 13-6. Santos-Rebouças Cíntia Barros, Abdalla Cláudia Bueno, Martins Paloma Aguia, Baldi Fábio José Rodrigues, Santos Jussara Mendonça, Motta Luciana Branco, de Borges Margarete Borges, Souza Dorotéia Rossi Silva, de Souza Pinhel Marcela Augusta, Laks Jerson, Pimentel Márcia Mattos Gonçalv |
Investigation of c9orf72 in 4 neurodegenerative disorders. Archives of neurology 2012 Dec 69 (12): 1583-90. Xi Zhengrui, Zinman Lorne, Grinberg Yakov, Moreno Danielle, Sato Christine, Bilbao Juan M, Ghani Mahdi, Hernández Isabel, Ruiz Agustín, Boada Mercè, Morón Francisco J, Lang Anthony E, Marras Connie, Bruni Amalia, Colao Rosanna, Maletta Raffaele G, Puccio Gianfranco, Rainero Innocenzo, Pinessi Lorenzo, Galimberti Daniela, Morrison Karen E, Moorby Catriona, Stockton Joanne D, Masellis Mario, Black Sandra E, Hazrati Lili-Naz, Liang Yan, van Haersma de With Jan, Fornazzari Luis, Villagra Roque, Rojas-Garcia Ricardo, Clarimón Jordi, Mayeux Richard, Robertson Janice, St George-Hyslop Peter, Rogaeva Ekateri |
The genetic contributions of SNCA and LRRK2 genes to Lewy Body pathology in Alzheimer's disease. Human molecular genetics 2014 Sep 23 (18): 4814-21. Linnertz Colton, Lutz Michael W, Ervin John F, Allen Jawara, Miller Natalie R, Welsh-Bohmer Kathleen A, Roses Allen D, Chiba-Falek Orn |
A Specific Diplotype H1j/H2 of the MAPT Gene Could Be Responsible for Parkinson's Disease with Dementia. Case reports in genetics 2020 2020 8813344. Smaili Imane, Hajjaj Imane, Razine Rachid, Tibar Houyam, Salmi Ayyoub, Bouslam Naima, Moussa Ahmed, Regragui Wafa, Bouhouche Ahm |
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