Human Genome Epidemiology Literature Finder
|
Records 1 - 10 (of 10 Records) |
| Query Trace: Disease and TOR1A[original query] |
|---|
| DYT1 mutations in early onset primary torsion dystonia and Parkinson disease patients in Chinese populations. Neuroscience letters 2009 Jan 450 (2): 117-21. Yang Jing-Fang, Wu Tao, Li Jian-Yu, Li Yong-Jie, Zhang Yan-Li, Chan P |
| Prevalence of THAP1 sequence variants in German patients with primary dystonia. Movement disorders : official journal of the Movement Disorder Society 2010 Sep 25 (12): 1982-6. Söhn Anne S, Glöckle Nicola, Doetzer Andrea Duarte, Deuschl Günther, Felbor Ute, Topka Helge R, Schöls Ludger, Riess Olaf, Bauer Peter, Müller Ulrich, Grundmann Kathr |
| Clinical features, DYT1 mutation screening and genotype-phenotype correlation in patients with dystonia from Iran. Medical principles and practice : international journal of the Kuwait University, Health Science Centre 2012 21 (5): 462-6. Akbari Mohammad Taghi, Zand Zahra, Shahidi Gholam Ali, Hamid Mohamm |
| SGCE mutations cause psychiatric disorders: clinical and genetic characterization. Brain : a journal of neurology 2013 Jan 136 (Pt 1): Pt 1. Peall KJ, Smith DJ, Kurian MA, Wardle M, Waite AJ, Hedderly T, Lin JP, Smith M, Whone A, Pall H, White C, Lux A, Jardine P, Bajaj N, Lynch B, Kirov G, O'Riordan S, Samuel M, Lynch T, King MD, Chinnery PF, Warner TT, Blake DJ, Owen MJ, Morris HR |
| TOR1A polymorphisms in a Russian cohort with primary focal/segmental dystonia. The International journal of neuroscience 2015 Sep 125 (9): 671-7. Timerbaeva Sofia L, Abramycheva Natalia Yu, Rebrova Olga Yu, Illarioshkin Sergey |
| Novel THAP1 variants in Brazilian patients with idiopathic isolated dystonia. Journal of the neurological sciences 2014 Sep 344 (1-2): 190-2. da Silva-Junior Francisco Pereira, dos Santos Camila Oliveira, Silva Sonia Maria Cesar Azevedo, Barbosa Egberto Reis, Borges Vanderci, Ferraz Henrique Ballalai, Limongi João Carlos Papaterra, Rocha Maria Sheila Guimarães, de Carvalho Aguiar Patric |
| Systematic TOR1A non-c.907_909delGAG variant analysis in isolated dystonia and controls. Parkinsonism & related disorders 2016 Jul . Zech Michael, Jochim Angela, Boesch Sylvia, Weber Sandrina, Meindl Tobias, Peters Annette, Gieger Christian, Mueller Joerg, Messner Michael, Ceballos-Baumann Andres, Poewe Werner, Haslinger Bernhard, Winkelmann Julia |
| Dystonia-Causing Mutations as a Contribution to the Etiology of Spasmodic Dysphonia. Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery 2016 May . de Gusmão Claudio M, Fuchs Tania, Moses Andrew, Multhaupt-Buell Trisha, Song Phillip C, Ozelius Laurie J, Franco Ramon A, Sharma Nut |
| Clinical and genetic features of cervical dystonia in a large multicenter cohort. Neurology. Genetics 2016 Jun 2 (3): e69. LeDoux Mark S, Vemula Satya R, Xiao Jianfeng, Thompson Misty M, Perlmutter Joel S, Wright Laura J, Jinnah H A, Rosen Ami R, Hedera Peter, Comella Cynthia L, Weissbach Anne, Junker Johanna, Jankovic Joseph, Barbano Richard L, Reich Stephen G, Rodriguez Ramon L, Berman Brian D, Chouinard Sylvain, Severt Lawrence, Agarwal Pinky, Stover Natividad |
| Deletion variant rs35153737 in TOR1A is associated with isolated dystonia in a Southwestern Chinese Population. Neuroscience letters 2017 Jul 657 1-4. Li Jiang, Long Yuzhou, Huang Xiaoqin, Chen Yuan, Chen Weikang, Liu Shang, Chu Jiayou, Yang Zhaoqing, Sun Hao, Fang Kew |
- Page last reviewed:Feb 1, 2024
- Content source: