Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 30 (of 43 Records) |
Query Trace: Optic Neuritis[original query] |
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Preliminary study on the association of AQP4 promoter polymorphism with anti-aquaporin-4 antibody positivity in southern Han Chinese patients with idiopathic demyelinating disorders of central nervous system. Journal of neuroimmunology 2013 Feb 255 (1-2): 75-80. Mai Weihua, Hu Xueqiang, Lu Zhengqi, Qiu Wei, Peng Fuhua, Wang Yu |
Association of multiple sclerosis susceptibility variants and early attack location in the CNS. PloS one 2013 8 (10): e75565. Mowry Ellen M, Carey Robert F, Blasco Maria R, Pelletier Jean, Duquette Pierre, Villoslada Pablo, Malikova Irina, Roger Elaine, Kinkel R Phillip, McDonald Jamie, Bacchetti Peter, Waubant Emmanuel |
MMP-2 -1575G/A polymorphism modifies the onset of optic neuritis as a first presenting symptom in MS? Journal of neuroimmunology 2015 Sep 286 13-5. Gašparovi? Iva, ?izmarevi? Nada Star?evi?, Lovre?i? Luca, Perkovi? Olivio, Lavtar Polona, Sep?i? Juraj, Jazbec Saša Šega, Kapovi? Miljenko, Peterlin Borut, Risti? Smilja |
Combinations of susceptibility genes are associated with higher risk for multiple sclerosis and imply disease course specificity. PloS one 2015 10 (5): e0127632. Akkad Denis A, Olischewsky Alexandra, Reiner Franziska, Hellwig Kerstin, Esser Sarika, Epplen Jörg T, Curk Tomaz, Gold Ralf, Haghikia Aid |
[Correlation of AQP4 gene polymorphism with NMO clinical phenotypes and its underlying mechanism]. Zhonghua yi xue za zhi 2015 Feb 95 (7): 501-6. Qiu Wei, Chang Yanyu, Li Rui, Long Youming, Huang Jianhua, Mai Weihua, Sun Xiaobo, Lu Zhengqi, Hu Xueqia |
Association Between the Single Nucleotide Polymorphism and the Level of Aquaporin-4 Protein Expression in Han and Minority Chinese with Inflammatory Demyelinating Diseases of the Central Nervous System. Molecular neurobiology 2015 Apr . Chu Lan, Dai Qingqing, Xu Zhu, He Dian, Wang Hao, Wang Qingsong, Zhang Yifan, Zhu Yingwu, Li Yuan, Cai Gang, Slavica Krantic, Allan Kermo |
No evidence of association between optic neuritis and secondary LHON mtDNA mutations in patients with multiple sclerosis. Mitochondrion 2017 Aug . Andalib Sasan, Talebi Mahnaz, Sakhinia Ebrahim, Farhoudi Mehdi, Sadeghi-Bazargani Homayoun, Masoudian Nooshin, Vafaee Manouchehr Seyedi, Gjedde Albe |
[Association analysis of cytokine receptors' genes polymorphisms with clinical features of multiple sclerosis]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 2016 116 (10. Vyp. 2): 10-15. Kulakova O G, Bashinskaya V V, Tsareva E Yu, Boiko A N, Favorova O O, Gusev E |
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 |
Association of Optic Neuritis with CYP4F2 Gene Single Nucleotide Polymorphism and IL-17A Concentration. Journal of ophthalmology 2018 2018 1686297. Banevicius Mantas, Vilkeviciute Alvita, Glebauskiene Brigita, Kriauciuniene Loresa, Liutkeviciene Ra |
Autoimmune and immunogenetic profile of patients with optic neuritis in a population-based cohort. Multiple sclerosis and related disorders 2018 Mar 21 97-102. Soelberg K, Nilsson A C, Nielsen C, Jarius S, Reindl M, Wildemann B, Lillevang S T, Asgari |
Association of MMP-2 (?1306 C/T) Gene Polymorphism with Predisposition to Optic Neuritis and Optic Neuritis Together with Multiple Sclerosis. Medicina (Kaunas, Lithuania) 2018 10 54 (2): . Liutkevi?ien? Rasa, Vilkevi?i?t? Alvita, Banevi?us Mantas, Miežyt? Raminta, Kriau?i?nien? Lore |
Early complement genes are associated with visual system degeneration in multiple sclerosis.
Brain : a journal of neurology 2019 Sep 142 (9): 2722-2736. Fitzgerald Kathryn C, Kim Kicheol, Smith Matthew D, Aston Sean A, Fioravante Nicholas, Rothman Alissa M, Krieger Stephen, Cofield Stacey S, Kimbrough Dorlan J, Bhargava Pavan, Saidha Shiv, Whartenby Katharine A, Green Ari J, Mowry Ellen M, Cutter Gary R, Lublin Fred D, Baranzini Sergio E, De Jager Philip L, Calabresi Peter |
Does CETP rs5882, rs708272, SIRT1 rs12778366, FGFR2 rs2981582, STAT3 rs744166, VEGFA rs833068, IL6 rs1800795 polymorphisms play a role in optic neuritis development? Ophthalmic genetics 2019 6 40 (3): 219-226. Gedvilaite Greta, Vilkeviciute Alvita, Kriauciuniene Loresa, Asmoniene Virginija, Liutkeviciene Ra |
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 |
MIF -173G/C polymorphism is associated with NMO disease severity. Journal of neuroimmunology 2019 Nov 339 577120. Brill Livnat, Vaknin-Dembinsky Adi, Zveik Omri, Haham Nitsan, Miller Keren, Benedek G |
Neurological phenotypes in patients with NLRP3-, MEFV-, and TNFRSF1A low-penetrance variants. Journal of neuroinflammation 2020 6 17 (1): 196. Mulazzani Elisabeth, Wagner Danny, Havla Joachim, Schlüter Miriam, Meinl Ingrid, Gerdes Lisa-Ann, Kümpfel Tan |
Associations between IL1RAP rs4624606, IL1RL1 rs1041973, IL-6 rs1800795, and HTRA1 rs11200638 gene polymorphisms and development of optic neuritis with or without multiple sclerosis. Ophthalmic genetics 2020 May 1-6. Stonys Valdas, Lindžiute Migle, Vilkeviciute Alvita, Gedvilaite Greta, Kriauciuniene Loresa, Banevicius Mantas, Žemaitiene Reda, Liutkeviciene Ra |
Association of VEGFA, TIMP-3, and IL-6 gene polymorphisms with predisposition to optic neuritis and optic neuritis with multiple sclerosis. Ophthalmic genetics 2020 10 42 (1): 35-44. Punyte Vaida, Vilkeviciute Alvita, Gedvilaite Greta, Kriauciuniene Loresa, Liutkeviciene Ra |
Association of RAGE rs1800624 and rs1800625 gene polymorphisms with predisposition to optic neuritis and optic neuritis together with multiple sclerosis. Ophthalmic genetics 2021 Aug 1-6. Kolonaite Gabriele, Vilkeviciute Alvita, Kriauciuniene Loresa, Gedvilaite Greta, Liutkeviciene Ra |
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 |
Ocular inflammatory diseases in children with familial Mediterranean fever: a true association or a coincidence? International ophthalmology 2021 11 42 (4): 1249-1257. Avar-Aydin Pinar Ozge, Cakar Nilgun, Ozcakar Zeynep Birsin, Yalcindag Nilufer, Yalcinkaya Fat |
HLA genotype-clinical phenotype correlations in multiple sclerosis and neuromyelitis optica spectrum disorders based on Japan MS/NMOSD Biobank data. Scientific reports 2021 Jan 11 (1): 607. Watanabe Mitsuru, Nakamura Yuri, Sato Shinya, Niino Masaaki, Fukaura Hikoaki, Tanaka Masami, Ochi Hirofumi, Kanda Takashi, Takeshita Yukio, Yokota Takanori, Nishida Yoichiro, Matsui Makoto, Nagayama Shigemi, Kusunoki Susumu, Miyamoto Katsuichi, Mizuno Masanori, Kawachi Izumi, Saji Etsuji, Ohashi Takashi, Shimohama Shun, Hisahara Shin, Nishiyama Kazutoshi, Iizuka Takahiro, Nakatsuji Yuji, Okuno Tatsusada, Ochi Kazuhide, Suzumura Akio, Yamamoto Ken, Kawano Yuji, Tsuji Shoji, Hirata Makoto, Sakate Ryuichi, Kimura Tomonori, Shimizu Yuko, Nagaishi Akiko, Okada Kazumasa, Hayashi Fumie, Sakoda Ayako, Masaki Katsuhisa, Shinoda Koji, Isobe Noriko, Matsushita Takuya, Kira Jun-Ic |
Association of HLA DRB1-DQB1 Haplotypes with the Risk for Neuromyelitis Optica among South Indians. Neurology India 0 70 (4): 1481-1486. Kanikannan Meena A, Kathgave Rakesh, Yareeda Sireesha, Katkam Shiva K, Kumaraswamy Konda, Kutala Vijay |
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 |
Mendelian randomization analysis reveals causal relationships between gut microbiome and optic neuritis. Human genetics 2022 12 . Liu Kangcheng, Wu Pengfei, Zou Jing, Fan Huimin, Hu Hanying, Cheng Yanhua, He Fei, Liu Jingying, You Zhipe |
Leber's hereditary optic neuropathy companied with multiple-related diseases. Frontiers in human neuroscience 2022 11 16 964550. Sun Ming-Ming, Zhou Huan-Fen, Sun Qiao, Li Hong-En, Liu Hong-Juan, Song Hong-Lu, Yang Mo, Teng Da, Wei Shi-Hui, Xu Quan-Ga |
The role of SIRT1 level and SIRT1 gene polymorphisms in optic neuritis patients with multiple sclerosis. Orphanet journal of rare diseases 2023 3 18 (1): 64. Kubiliute Aleksandra, Gedvilaite Greta, Vilkeviciute Alvita, Kriauciuniene Loresa, Bruzaite Akvile, Zaliuniene Dalia, Liutkeviciene Ra |
Association of retinal vessel pathology and brain atrophy in relapsing-remitting multiple sclerosis. Frontiers in immunology 2023 12 14 1284986. Eva Feodora Romahn, Tun Wiltgen, Matthias Bussas, Lilian Aly, Rebecca Wicklein, Christina Noll, Achim Berthele, Vera Dehmelt, Christian Mardin, Claus Zimmer, Thomas Korn, Bernhard Hemmer, Jan S Kirschke, Mark Mühlau, Benjamin Kni |
Optic Neuritis: The Influence of Gene Polymorphisms and Serum Levels of STAT4 (rs10181656, rs7574865, rs7601754, rs10168266). Journal of clinical medicine 2024 1 13 (1): . Greta Gedvilaite, Monika Duseikait?, Gabriel? Dubinskaite, Loresa Kriauciuniene, Reda Zemaitiene, Rasa Liutkevicie |
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- Page last updated:Apr 22, 2024
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