Human Genome Epidemiology Literature Finder
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Query Trace: Neuromyelitis Optica Spectrum Disorder[original query] |
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Distinct genetic and infectious profiles in Japanese neuromyelitis optica patients according to anti-aquaporin 4 antibody status. Journal of neurology, neurosurgery, and psychiatry 2012 Oct . Yoshimura S, Isobe N, Matsushita T, Yonekawa T, Masaki K, Sato S, Kawano Y, Kira JI |
A prospective case-control study comparing optical coherence tomography characteristics in neuromyelitis optica spectrum disorder- optic neuritis and idiopathic optic neuritis. BMC ophthalmology 2018 9 18 (1): 247. Zhao Xiujuan, Qiu Wei, Zhang Yuxin, Luo Yan, Zhang Xiulan, Lu Lin, Yang H |
Mutation of the cellular adhesion molecule NECL2 is associated with neuromyelitis optica spectrum disorder. Journal of the neurological sciences 2018 4 388 133-138. Xu Yan, Li Liang, Ren Hai-Tao, Yin Bin, Yuan Jian-Gang, Peng Xiao-Zhong, Qiang Bo-Qin, Cui Li-Yi |
The GTF2I rs117026326 polymorphism is associated with neuromyelitis optica spectrum disorder but not with multiple sclerosis in a Northern Han Chinese population. Journal of neuroimmunology 2019 Aug 337 577045. Liang Hudong, Gao Wenjing, Liu Xianjun, Liu Jingyao, Mao Xijing, Yang Mengge, Long Xixi, Zhou Yang, Zhang Qingxiang, Zhu Jie, Wang Shaofeng, Jin T |
Next-generation sequencing identifies contribution of both class I and II HLA genes on susceptibility of multiple sclerosis in Japanese. Journal of neuroinflammation 2019 Aug 16 (1): 162. Ogawa Kotaro, Okuno Tatsusada, Hosomichi Kazuyoshi, Hosokawa Akiko, Hirata Jun, Suzuki Ken, Sakaue Saori, Kinoshita Makoto, Asano Yoshihiro, Miyamoto Katsuichi, Inoue Ituro, Kusunoki Susumu, Okada Yukinori, Mochizuki Hide |
Association Between BDNF Val66Met Polymorphism and Optic Neuritis Damage in Neuromyelitis Optica Spectrum Disorder. Frontiers in neuroscience 2019 13 1236. Shen Ting, Gupta Vivek, Yiannikas Con, Klistorner Alexander, Graham Stuart L, You Yu |
HLA-G Ins/Del polymorphism and +3142C/G SNP are not related to neuromyelitis optica spectrum disorder (NMOSD) development, disability status or anti-aquaporin 4 presence in Brazilian patients. Journal of neuroimmunology 2019 11 339 577112. Gomes Nathália Augusta, Silva Pollyanna Cristina, Teixeira Ygor Tiago, Eufrazio Patrícia, Souza Alessandra D, Rojas Hugo, Brant Renata, Gomes Neto Antônio, Christo Paulo Pereira, Simões Renata Toscano, Fernandes Karla Simo |
Common genetic variants in PRRC2A are associated with both neuromyelitis optica spectrum disorder and multiple sclerosis in Han Chinese population. Journal of neurology 2020 Aug . Zhang Juan, Chen Mei-Jiao, Zhao Gui-Xian, Li Hong-Fu, Wu Lei, Xu Yong-Feng, Liao Yajin, Yuan Zengqiang, Wu Zhi-Yi |
IRAK1 polymorphisms are associated with susceptibility to neuromyelitis optica spectrum disorder. Multiple sclerosis and related disorders 2020 3 37 101438. Shi Ziyan, Chen Hongxi, Du Qin, Zhang Ying, Zhang Qin, Qiu Yuhan, Zhao Zhengyang, Wang Jiancheng, Yang Mu, Zhou Hong |
Associations of IRAK1 Gene Polymorphisms and mRNA Expression With NMOSD Risk in the Northern Chinese Han Population. Frontiers in neurology 2021 12 661791. Yan Hongjing, Guo Ruoyi, Chen Weifeng, Xi Xutao, Wang Lianchang, Ma Jianxun, Li B |
Interaction of HLA Class II rs9272219 and TMPO rs17028450 (Arg690Cys) Variants Affects Neuromyelitis Optica Spectrum Disorder Susceptibility in an Admixed Mexican Population. Frontiers in genetics 2021 8 12 647343. Rosas-Madrigal Sandra, Villarreal-Molina María Teresa, Flores-Rivera José, Rivas-Alonso Verónica, Macias-Kauffer Luis Rodrigo, Ordoñez Graciela, Chima-Galán María Del Carmen, Acuña-Alonzo Víctor, Macín-Pérez Gastón, Barquera Rodrigo, Granados Julio, Valle-Rios Ricardo, Corona Teresa, Carnevale Alessandra, Romero-Hidalgo Sand |
Whole-exome sequencing reveals the major genetic factors contributing to neuromyelitis optica spectrum disorder in Chinese patients with aquaporin 4-IgG seropositivity. European journal of neurology 2021 Feb . Zhong Xiaonan, Chen Chen, Sun Xiaobo, Wang Jingqi, Li Rui, Chang Yanyu, Fan Ping, Wang Yuge, Wu Yunting, Peng Lisheng, Lu Zhengqi, Qiu W |
Effect of inosine monophosphate dehydrogenase-1 gene polymorphisms on mycophenolate mofetil effectiveness in neuromyelitis optica spectrum disorder patients. Multiple sclerosis and related disorders 2021 Jan 49 102779. Liu Lanzhi, Luo Zhaohui, Liu Fan, Shang Danqing, Qiu Dongxu, Jiao Xiao, Zhou Xiaoliang, Chen Si, Wu Junfang, Li Ji |
Association Analysis Between HLA-DQA1 Loci and Neuromyelitis Optica Spectrum Disorder in a Han Chinese Population. The neurologist 2021 12 27 (4): 164-167. Zhou Lili, He Zhiyong, Zhu Lanbing, Zhu Juan-Juan, Zhu Jian-Hong, Pan Jial |
BLK polymorphisms and expression level in neuromyelitis optica spectrum disorder. CNS neuroscience & therapeutics 2021 Oct . Yin Bo-Wen, Li Bin, Mehmood Arshad, Yuan Congcong, Song Shuang, Guo Ruo-Yi, Zhang Lu, Ma Tianzhao, Guo |
Myelin oligodendrocyte glycoprotein-associated disease is associated with BANK1, RNASET2 and TNIP1 polymorphisms. Journal of neuroimmunology 2022 Aug 372 577937. Shu Yaqing, Ma Xiaoyu, Chen Chen, Wang Yuge, Sun Xiaobo, Zhang Liang, Lu Zhengqi, Petersen Frank, Qiu Wei, Yu Xinh |
A CD33 frameshift variant is associated with neuromyelitis optica spectrum disorders. Biomedical journal 2021 12 44 (6 Suppl 1): S93-S100. Huang Yu-Ju, Lee Jun-Jun, Fan Wen-Lan, Hsu Che-Wei, Tsai Nai-Wen, Lu Cheng-Hsien, Chang Wen-Neng, Tsai Meng-H |
ABCB1 gene polymorphisms impact the effect of high-dose intravenous methylprednisolone therapy on optic neuritis associated with AQP4-IgG-positive neuromyelitis optica spectrum disorder. Journal of clinical pharmacy and therapeutics 2022 4 47 (9): 1379-1387. Dai Yuyang, Ni Siyang, Wu Feng, Guo Shaojie, Zhao Xiuli, Wang Jiaw |
Clinical and genetic analysis of familial neuromyelitis optica spectrum disorder in Chinese: associated with ubiquitin-specific peptidase USP18 gene variants. Journal of neurology, neurosurgery, and psychiatry 2022 11 93 (12): 1269-1275. Chang Yanyu, Zhou Luyao, Zhong Xiaonan, Shi Ziyan, Sun Xiaobo, Wang Yuge, Li Rui, Long Youming, Zhou Hongyu, Quan Chao, Kermode Allan G, Yu Qingfen, Qiu W |
Causal Relations between Prodromal Infection and Neuromyelitis Optica Spectrum Disorder: A Mendelian Randomization Study. European journal of neurology 2023 8 . Liang Wang, Lei Zhou, Jingzi ZhangBao, Wenjuan Huang, Hongmei Tan, Yuxin Fan, Chuanzhen Lu, Jian Yu, Min Wang, Jiahong Lu, Chongbo Zhao, Tiansong Zhang, Chao Qu |
COVID-19 and the risk of neuromyelitis optica spectrum disorder: a Mendelian randomization study. Frontiers in immunology 2023 8 14 1207514. Dongren Sun, Qin Du, Rui Wang, Ziyan Shi, Hongxi Chen, Hongyu Zh |
Tailoring Rituximab According to CD27-Positive B-Cell versus CD19-Positive B-Cell Monitoring in Neuromyelitis Optica Spectrum Disorder and MOG-Associated Disease: Results from a Single-Center Study. Neurology and therapy 2023 5 . Nicolò Bruschi, Maria Malentacchi, Simona Malucchi, Francesca Sperli, Serena Martire, Arianna Sala, Paola Valentino, Antonio Bertolotto, Marisa Pautasso, Marco Alfonso Capobian |
Inebilizumab reduces neuromyelitis optica spectrum disorder risk independent of FCGR3A polymorphism. Annals of clinical and translational neurology 2023 10 . Ho Jin Kim, Orhan Aktas, Kristina R Patterson, Schaun Korff, Amy Kunchok, Jeffrey L Bennett, Brian G Weinshenker, Friedemann Paul, Hans-Peter Hartung, Daniel Cimbora, Michael A Smith, Nanette Mittereder, William A Rees, Dewei She, Bruce A C Cr |
Association between TIMP1 polymorphism and female neuromyelitis optica spectrum disorder in Chinese population. Heliyon 2024 9 10 (17): e37091. Hongjing Yan, Yining Wang, Ruoyi Guo, Zhen Jia, Jia Liu, Bin |
Association between FOXP3 polymorphisms and expression and neuromyelitis optica spectrum disorder risk in the Northern Chinese Han population. Translational neuroscience 2024 4 15 (1): 20220337. Jing Liu, Gaoning Wang, Jiahe Yang, Yulin Wang, Ruoyi Guo, Bin |
FCGR3A-V158F gene polymorphism: A potential predictor for rituximab dosing optimization in Chinese patients with neuromyelitis optica spectrum disorder. Multiple sclerosis and related disorders 2024 4 86 105600. Lei Cui, Jinsong Jiao, Yeqiong Zhang, Renbin Wang, Dantao Peng, Yujuan Jiao, Weihe Zha |
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