Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 20 (of 20 Records) |
Query Trace: Myelitis[original query] |
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Modification of Multiple Sclerosis Phenotypes by African Ancestry at HLA. Archives of neurology 2009 Feb 66 (2): 226-33. Cree Bruce A C, Reich David E, Khan Omar, De Jager Philip L, Nakashima Ichiro, Takahashi Toshiyuki, Bar-Or Amit, Tong Christine, Hauser Stephen L, Oksenberg Jorge |
Common CYP7A1 promoter polymorphism associated with risk of neuromyelitis optica. Neurobiology of disease 2010 Feb 37 (2): 349-55. Kim Ho Jin, Park Hyun-Young, Kim Eunkyung, Lee Kwang-Soo, Kim Kwang-Kuk, Choi Byung-Ok, Kim Seung Min, Bae Joon Seol, Lee Soo Ok, Chun Ji Yong, Park Tae Joon, Cheong Hyun Sub, Jo Inho, Shin Hyoung D |
Association of the HLA-DPB1*0501 allele with anti-aquaporin-4 antibody positivity in Japanese patients with idiopathic central nervous system demyelinating disorders. Tissue antigens 2009 Feb 73 (2): 171-6. Matsushita T, Matsuoka T, Isobe N, Kawano Y, Minohara M, Shi N, Nishimura Y, Ochi H, Kira |
HLA-DPB1*0201 is associated with susceptibility to atopic myelitis in Japanese. Journal of neuroimmunology 2012 Oct 251 (1-2): 110-3. Sato Shinya, Isobe Noriko, Yoshimura Satoshi, Kanamori Yuji, Masaki Katsuhisa, Matsushita Takuya, Kira Jun-Ic |
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 |
Analysis of prognostic factors associated with longitudinally extensive transverse myelitis. Multiple sclerosis (Houndmills, Basingstoke, England) 2012 Oct . Sepúlveda M, Blanco Y, Rovira A, Rio J, Mendibe M, Llufriu S, Gabilondo I, Villoslada P, Castilló J, Corral J, Ayuso T, Iñiguez C, Santos S, Guijarro C, Ramió-Torrentà L, Sempere AP, Olascoaga J, Graus F, Montalban X, Saiz A |
[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 |
Significant Association Between Fc Receptor-Like 3 Polymorphisms (-1901A>G and -658C>T) and Neuromyelitis Optica (NMO) Susceptibility in the Chinese Population. Molecular neurobiology 2015 Jan . Wang Xinling, Yu Tao, Yan Qichang, Wang Wei, Meng Nan, Li Xuejiao, Luo Yaho |
Aquaporin-4-autoimmunity in patients with systemic lupus erythematosus: A predominantly population-based study. Multiple sclerosis (Houndmills, Basingstoke, England) 2017 Mar 1352458517699791. Asgari Nasrin, Jarius Sven, Laustrup Helle, Skejoe Hanne Pb, Lillevang Soeren T, Weinshenker Brian G, Voss An |
Familial monophasic acute transverse myelitis due to the pathogenic variant in VPS37A. Neurology. Genetics 2018 2 4 (1): e213. Mealy Maureen A, Nam Tai-Seung, Pardo Santiago J, Pardo Carlos A, Sobreira Nara L, Avramopoulos Dimitrios, Valle David, Burns Kathleen H, Levy Micha |
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 |
Genetic factors for susceptibility to and manifestations of neuromyelitis optica. Annals of clinical and translational neurology 2020 9 7 (11): 2082-2093. Matsushita Takuya, Masaki Katsuhisa, Isobe Noriko, Sato Shinya, Yamamoto Ken, Nakamura Yuri, Watanabe Mitsuru, Suenaga Toshihiko, Kira Jun-Ichi, |
Impact of multiple sclerosis risk loci in postinfectious neurological syndromes. Multiple sclerosis and related disorders 2020 Jun 44 102326. Martinelli-Boneschi Filippo, Currò Riccardo, Santoro Silvia, Berzero Giulia, Sorosina Melissa, Ferrè Laura, Mascia Elisabetta, Peroni Silvia, Comi Giancarlo, Gugliemi Angelo, Vegezzi Elisa, Callegari Ilaria, Filippi Massimo, Cortese Andrea, Esposito Federica, Clarelli Ferdinando, Marchioni Enri |
HLA-B27 association of autoimmune encephalitis induced by PD-L1 inhibitor. Annals of clinical and translational neurology 2020 10 7 (11): 2243-2250. Chang Hyeyeon, Shin Yong-Won, Keam Bhumsuk, Kim Miso, Im Seock-Ah, Lee Soon-T |
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 |
Long-Term Outcome of a Series of Patients With Narcolepsy Type 1 and Comorbidity With Immunopathological and Autoimmune Diseases. Journal of clinical medicine research 2022 9 14 (8): 309-314. Martinez-Orozco Francisco J, Fernandez-Arquero Miguel, Vicario Jose L, Lillo-Triguero Laura, Ameyugo Elena, Peraita-Adrados Ro |
Patients with laboratory criteria of anti-phospholipid syndrome and 'non-criteria' manifestations: a multicenter cohort. Scandinavian journal of rheumatology 2022 6 52 (2): 190-195. Pires da Rosa G, Ferreira E, Sousa-Pinto B, Bettencourt P, Espinosa G, Cervera |
A case of refractory systemic lupus erythematosus with monocytosis exhibiting somatic KRAS mutation. Inflammation and regeneration 2022 4 42 (1): 10. Law Sze-Ming, Akizuki Shuji, Morinobu Akio, Ohmura Koichi |
What Kept Back on the Mirror of COVID-19-Related Acute Transverse Myelitis? A Genetic Background! Iranian journal of child neurology 2023 4 17 (2): 143-147. Reza Sinaei, Sara Pezeshki, Roya Sina |
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- Page last updated:Apr 16, 2024
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