Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Atrophy and SQSTM1[original query] |
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| Associations between multiple system atrophy and polymorphisms of SLC1A4, SQSTM1, and EIF4EBP1 genes. Movement disorders : official journal of the Movement Disorder Society 2008 Jun 23 (8): 1161-7. Soma Hiroyuki, Yabe Ichiro, Takei Asako, Fujiki Naoto, Yanagihara Tetsuro, Sasaki Hiden |
| Neuroimaging Correlates of Frontotemporal Dementia Associated with SQSTM1 Mutations. Journal of Alzheimer's disease : JAD 2016 May . Luis Elkin, Ortiz Alexandra, Eudave Luis, Ortega-Cubero Sara, Borroni Barbara, van der Zee Julie, Gazzina Stefano, Caroppo Paola, Rubino Elisa, D'Agata Federico, Le Ber Isabelle, Santana Isabel, Cunha Gil, Almeida Maria R, Boutoleau-Bretonnière Claire, Hannequin Didier, Wallon David, Rainero Innocenzo, Galimberti Daniela, Van Broeckhoven Christine, Pastor Maria A, Pastor P |
| Noncoding repeat expansions for ALS in Japan are associated with the ATXN8OS gene. Neurology. Genetics 2018 8 4 (4): e252. Hirano Makito, Samukawa Makoto, Isono Chiharu, Saigoh Kazumasa, Nakamura Yusaku, Kusunoki Susu |
| Genetic Spectrum and Clinical Heterogeneity of Chinese Frontotemporal Dementia Patients: Data from PUMCH Dementia Cohort. Journal of Alzheimer's disease : JAD 2022 Aug . Dong Liling, Wang Jie, Liu Caiyan, Li Jie, Mao Chenhui, Huang Xinying, Chu Shanshan, Peng Bin, Cui Liying, Gao Ji |
| Analysis of Structural Variants Previously Associated With ALS in Europeans Highlights Genomic Architectural Differences in Africans. Neurology. Genetics 2023 6 9 (4): e200077. Nomakhosazana R Monnakgotla, Amokelani C Mahungu, Jeannine M Heckmann, Gerrit Botha, Nicola J Mulder, Gang Wu, Evadnie Rampersaud, Jason Myers, Marka Van Blitterswijk, Rosa Rademakers, J Paul Taylor, Joanne Wuu, Michael Benatar, Melissa N |
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