Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: Sclerosis and ANXA11[original query] |
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Genetic analysis of ANXA11 variants in a Han Chinese cohort with amyotrophic lateral sclerosis in Taiwan. Neurobiology of aging 2018 Jul . Tsai Pei-Chien, Liao Yi-Chu, Jih Kang-Yang, Soong Bing-Wen, Lin Kon-Ping, Lee Yi-Chu |
ANXA11 mutations prevail in Chinese ALS patients with and without cognitive dementia. Neurology. Genetics 2018 5 4 (3): e237. Zhang Kang, Liu Qing, Liu Keqiang, Shen Dongchao, Tai Hongfei, Shu Shi, Ding Qingyun, Fu Hanhui, Liu Shuangwu, Wang Zhili, Li Xiaoguang, Liu Mingsheng, Zhang Xue, Cui Liyi |
ALS Genes in the Genomic Era and their Implications for FTD. Trends in genetics : TIG 2018 4 34 (6): 404-423. Nguyen Hung Phuoc, Van Broeckhoven Christine, van der Zee Jul |
Two rare variants of the ANXA11 gene identified in Chinese patients with amyotrophic lateral sclerosis. Neurobiology of aging 2019 02 74 235.e9-235.e12. Liu Xiangyi, Wu Chujun, He Ji, Zhang Nan, Fan Dongshe |
Unique characteristics of the genetics epidemiology of amyotrophic lateral sclerosis in China. Science China. Life sciences 2019 3 62 (4): 517-525. Wei Qianqian, Chen Xueping, Chen Yongping, Ou Ruwei, Cao Bei, Hou Yanbing, Zhang Lingyu, Shang Hui-Fa |
Genetic epidemiology of familial ALS in Brazil. Neurobiology of aging 2021 2 102 227.e1-227.e4. Nunes Gonçalves João Pedro, Leoni Tauana Bernardes, Martins Melina Pazian, Peluzzo Thiago Mazzo, Dourado Mario Emílio T, Saute Jonas Alex M, Paranhos Miranda Covaleski Anna Paula, Bulle de Oliveira Acary Souza, Claudino Rinaldo, Marques Wilson, Nucci Anamarli, França Marcondes |
Generation of six induced pluripotent stem cell lines from patients with amyotrophic lateral sclerosis with associated genetic mutations in either FUS or ANXA11. Stem cell research 2021 2 52 102246. Hedges Erin C, Topp Simon, Shaw Christopher E, Nishimura Agnes |
Re-analysis of the Hungarian amyotrophic lateral sclerosis population and evaluation of novel ALS genetic risk variants. Neurobiology of aging 2022 Aug 116 1-11. Nagy Zsófia Flóra, Pál Margit, Salamon András, Kafui Esi Zodanu Gloria, Füstös Dalma, Klivényi Péter, Széll Már |
Mutation spectrum of chinese amyotrophic lateral sclerosis patients with frontotemporal dementia. Orphanet journal of rare diseases 2022 11 17 (1): 404. Yang Xunzhe, Sun Xiaohai, Liu Qing, Liu Liyang, Li Jinyue, Cai Zhengyi, Zhang Kang, Liu Shuangwu, He Di, Shen Dongchao, Liu Mingsheng, Cui Liying, Zhang X |
Genetic analysis of and clinical characteristics associated with ANXA11 variants in a Chinese cohort with amyotrophic lateral sclerosis. Neurobiology of disease 2022 10 175 105907. Jiang Qirui, Lin Junyu, Wei Qianqian, Li Chunyu, Hou Yanbing, Cao Bei, Zhang Lingyu, Ou Ruwei, Liu Kuncheng, Yang Tianmi, Xiao Yi, Shang Huifa |
Revealing the Mutational Spectrum in Southern Africans With Amyotrophic Lateral Sclerosis. Neurology. Genetics 2022 Feb 8 (1): e654. Nel Melissa, Mahungu Amokelani C, Monnakgotla Nomakhosazana, Botha Gerrit R, Mulder Nicola J, Wu Gang, Rampersaud Evadnie, van Blitterswijk Marka, Wuu Joanne, Cooley Anne, Myers Jason, Rademakers Rosa, Taylor J Paul, Benatar Michael, Heckmann Jeannine |
Semantic variant primary progressive aphasia with a pathogenic variant p.Asp40Gly in the ANXA11 gene. European journal of neurology 2022 Oct 29 (10): 3124-3126. Kim Eun-Joo, Moon So Young, Kim Hee-Jin, Jung Na-Yeon, Lee Sun Min, Kim Young E |
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- Page last updated:Apr 22, 2024
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