Human Genome Epidemiology Literature Finder
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Records 1 - 13 (of 13 Records) |
| Query Trace: Amyotrophic Lateral Sclerosis and DCTN1[original query] |
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| The p150 subunit of dynactin (DCTN1) gene in multiple sclerosis. Acta neurologica Scandinavica 2007 Oct 116 (4): 231-4. Münch C, Meyer R, Linke P, Meyer T, Ludolph A C, Haas J, Hemmer |
| Characterization of DCTN1 genetic variability in neurodegeneration. Neurology 2009 Jun 72 (23): 2024-8. Vilariño-Güell C, Wider C, Soto-Ortolaza A I, Cobb S A, Kachergus J M, Keeling B H, Dachsel J C, Hulihan M M, Dickson D W, Wszolek Z K, Uitti R J, Graff-Radford N R, Boeve B F, Josephs K A, Miller B, Boylan K B, Gwinn K, Adler C H, Aasly J O, Hentati F, Destée A, Krygowska-Wajs A, Chartier-Harlin M-C, Ross O A, Rademakers R, Farrer M |
| Identify mutation in amyotrophic lateral sclerosis cases using HaloPlex target enrichment system. Neurobiology of aging 2014 Dec 35 (12): 2881.e11-5. Liu Zhi-Jun, Li Hong-Fu, Tan Guo-He, Tao Qing-Qing, Ni Wang, Cheng Xue-Wen, Xiong Zhi-Qi, Wu Zhi-Yi |
| Defining neurodegeneration on Guam by targeted genomic sequencing. Annals of neurology 2015 Mar 77 (3): 458-68. Steele John C, Guella Ilaria, Szu-Tu Chelsea, Lin Michelle K, Thompson Christina, Evans Daniel M, Sherman Holly E, Vilariño-Güell Carles, Gwinn Katrina, Morris Huw, Dickson Dennis W, Farrer Matthew |
| DCTN1 gene analysis in Chinese patients with sporadic amyotrophic lateral sclerosis. PloS one 2017 12 (8): e0182572. Liu Xiangyi, Yang Lipeng, Tang Lu, Chen Lu, Liu Xiaolu, Fan Dongshe |
| Identification and characterization of novel and rare susceptible variants in Indian amyotrophic lateral sclerosis patients. Neurogenetics 2019 8 20 (4): 197-208. Narain Priyam, Padhi Aditya K, Dave Upma, Mishra Dibyakanti, Bhatia Rohit, Vivekanandan Perumal, Gomes Jam |
| Comparison of the clinical and genetic features of amyotrophic lateral sclerosis across Cuban, Uruguayan and Irish clinic-based populations. Journal of neurology, neurosurgery, and psychiatry 2019 3 90 (6): 659-665. Ryan Marie, Zaldívar Vaillant Tatiana, McLaughlin Russell L, Doherty Mark A, Rooney James, Heverin Mark, Gutierrez Joel, Lara-Fernández Gloria Esther, Pita Rodríguez Mariana, Hackembruch Jochen, Perna Abayubá, Vazquez Maria Cristina, Musio Marco, Ketzoian Carlos N, Logroscino Giancarlo, Hardiman Or |
| 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 Spectrum and Variability in Chinese Patients with Amyotrophic Lateral Sclerosis. Aging and disease 2019 Dec 10 (6): 1199-1206. Liu Zhi-Jun, Lin Hui-Xia, Wei Qiao, Zhang Qi-Jie, Chen Cong-Xin, Tao Qing-Qing, Liu Gong-Lu, Ni Wang, Gitler Aaron D, Li Hong-Fu, Wu Zhi-Yi |
| SOD1-related ALS with anticipation in a large family from Martinique. Amyotrophic lateral sclerosis & frontotemporal degeneration 2021 3 22 (7-8): 545-551. Giguet-Valard Anna-Gaelle, Bellance Rémi, Jeannin Séverine, Duclos Sophie, Olive Pascale, Allard-Saint-Albin Oriane, Cazeneuve Cécile, Clot Fabienne, Sophie Pittion-Vouyovitch, Barnetche Thomas, Smith-Ravin Juliette, Goizet Cyr |
| Genetic analysis of ALS cases in the isolated island population of Malta. European journal of human genetics : EJHG 2021 1 29 (4): 604-614. Borg Rebecca, Farrugia Wismayer Maia, Bonavia Karl, Farrugia Wismayer Andrew, Vella Malcolm, van Vugt Joke J F A, Kenna Brendan J, Kenna Kevin P, Vassallo Neville, Veldink Jan H, Cauchi Ruben |
| Exome Sequencing of a Portuguese Cohort of Frontotemporal Dementia Patients: Looking Into the ALS-FTD Continuum. Frontiers in neurology 2022 13 886379. Tábuas-Pereira Miguel, Santana Isabel, Gibbons Elizabeth, Paquette Kimberly, Almeida Maria Rosário, Baldeiras Inês, Bras Jose, Guerreiro Ri |
| [Genetic distribution in Chinese patients with hereditary peripheral neuropathy]. Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2022 10 54 (5): 874-883. Liu X X, Duan X H, Zhang S, Sun A P, Zhang Y S, Fan D |
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