Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: Syndrome and FUS[original query] |
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FUS mutations in amyotrophic lateral sclerosis: clinical, pathological, neurophysiological and genetic analysis. Journal of neurology, neurosurgery, and psychiatry 2010 Jun 81 (6): 639-45. Blair Ian P, Williams Kelly L, Warraich Sadaf T, Durnall Jennifer C, Thoeng Annora D, Manavis Jim, Blumbergs Peter C, Vucic Steve, Kiernan Matthew C, Nicholson Garth |
The most common type of FTLD-FUS (aFTLD-U) is associated with a distinct clinical form of frontotemporal dementia but is not related to mutations in the FUS gene. Acta neuropathologica 2011 Jul 122 (1): 99-110. Snowden Julie S, Hu Quan, Rollinson Sara, Halliwell Nicola, Robinson Andrew, Davidson Yvonne S, Momeni Parastoo, Baborie Atik, Griffiths Timothy D, Jaros Evelyn, Perry Robert H, Richardson Anna, Pickering-Brown Stuart M, Neary David, Mann David M |
CD40 polymorphisms in Han Chinese patients with Fuch uveitis syndrome. Molecular vision 2011 17 2469-72. Chen Feilan, Hou Shengping, Jiang Zhengxuan, Li Fuzhen, Chen Yuanyuan, Kijlstra Aize, Yang Peize |
Lack of association of miR-146a and Ets-1 gene polymorphisms with Fuchs uveitis syndrome in Chinese Han patients. Molecular vision 2012 18 426-30. Zhou Qingyun, Kijlstra Aize, Hou Shengping, Yu Hongsong, Zhang Xuedong, Li Xinyu, Xiao Xiang, Yang Peize |
Comparison of the clinical and cognitive features of genetically positive ALS patients from the largest tertiary center in Serbia. Journal of neurology 2017 Jun 264 (6): 1091-1098. Marjanovic Ivan V, Selak-Djokic Biljana, Peric Stojan, Jankovic Milena, Arsenijevic Vladimir, Basta Ivana, Lavrnic Dragana, Stefanova Elka, Stevic Zori |
ALS and CHARGE syndrome: a clinical and genetic study. Acta neurologica Belgica 2018 10 118 (4): 629-635. Ungaro Carmine, Citrigno Luigi, Trojsi Francesca, Sprovieri Teresa, Gentile Giulia, Muglia Maria, Monsurrò Maria Rosaria, Tedeschi Gioacchino, Cavallaro Sebastiano, Conforti Francesca Lui |
The Frequency of Genetic Mutations Associated With Behavioral Variant Frontotemporal Dementia in Chinese Han Patients. Frontiers in aging neuroscience 2021 13 699836. Liu Li, Cui Bo, Chu Min, Cui Yue, Jing Donglai, Li Dan, Xie Kexin, Kong Yu, Xia Tianxinyu, Wang Chaodong, Wu Liyo |
Clinical and genetic characteristics of 1672 cases of amyotrophic lateral sclerosis in China: a single-center retrospective study. Journal of neurology 2024 6 . Dongchao Shen, Xunzhe Yang, Di He, Kang Zhang, Shuangwu Liu, Xiaohan Sun, Jinyue Li, Zhengyi Cai, Mingsheng Liu, Xue Zhang, Qing Liu, Liying C |
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