Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: Dystonia and TH[original query] |
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Low frequency of Parkin, Tyrosine Hydroxylase, and GTP Cyclohydrolase I gene mutations in a Danish population of early-onset Parkinson's Disease. European journal of neurology : the official journal of the European Federation of Neurological Societies 2006 Apr 13 (4): 385-90. Hertz J M, Ostergaard K, Juncker I, Pedersen S, Romstad A, Møller L B, Güttler F, Dupont |
Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystonia. Brain : a journal of neurology 2009 Jul 132 (Pt 7): 1753-63. Clot Fabienne, Grabli David, Cazeneuve Cécile, Roze Emmanuel, Castelnau Pierre, Chabrol Brigitte, Landrieu Pierre, Nguyen Karine, Ponsot Gérard, Abada Myriem, Doummar Diane, Damier Philippe, Gil Roger, Thobois Stéphane, Ward Alana J, Hutchinson Michael, Toutain Annick, Picard Fabienne, Camuzat Agnès, Fedirko Estelle, Sân Chankannira, Bouteiller Delphine, LeGuern Eric, Durr Alexandra, Vidailhet Marie, Brice Alexis, |
A rare novel deletion of the tyrosine hydroxylase gene in Parkinson disease. Human mutation 2010 Oct 31 (10): E1767-71. Bademci Güney, Edwards Todd L, Torres Andre L, Scott William K, Züchner Stephan, Martin Eden R, Vance Jeffery M, Wang Liyo |
Cervical dystonia and genetic common variation in the dopamine pathway. Parkinsonism & related disorders 2013 Mar 19 (3): 346-9. Groen Justus L, Simón-Sánchez Javier, Ritz Katja, Bochdanovits Zoltán, Fang Yue, van Hilten Jacobus J, Aramideh Majid, van de Warrenburg Bart P, Boon Agnita J W, Baas Frank, Heutink Peter, Tijssen Marina A |
Low frequency of GCH1 and TH mutations in Parkinson's disease. Parkinsonism & related disorders 2016 May . Rengmark Aina, Pihlstrøm Lasse, Linder Jan, Forsgren Lars, Toft Mathi |
Study of GCH1 and TH genes in Chinese patients with Parkinson's disease. Neurobiology of aging 2018 08 68 159.e3-159.e6. Yan Ya-Ping, Zhang Bo, Shen Ting, Si Xiao-Li, Guo Zhang-Yu, Tian Jun, Xu Cong-Ying, Zhang Bao-Ro |
Clinical and Genetic Heterogeneity in a Cohort of Chinese Children With Dopa-Responsive Dystonia. Frontiers in pediatrics 2020 3 8 83. Chen Yan, Bao Xinhua, Wen Yongxin, Wang Jiaping, Zhang Qingping, Yan Jiay |
A preliminary exome sequence in three patients with tardive dystonia. Psychiatric genetics 2019 Dec . Kanahara Nobuhisa, Nakata Yusuke, Iyo Masao |
Genetic analysis of dystonia-related genes in Parkinson's disease. Frontiers in aging neuroscience 2023 6 15 1207114. Yige Wang, Yuwen Zhao, Hongxu Pan, Qian Zeng, Xiaoxia Zhou, Yaqin Xiang, Zhou Zhou, Qian Xu, Qiying Sun, Jieqiong Tan, Xinxiang Yan, Jinchen Li, Jifeng Guo, Beisha Tang, Qiao Yu, Zhenhua L |
Whole-exome sequencing in a cohort of Chinese patients with isolated cervical dystonia. Heliyon 2024 6 10 (11): e31885. Rui Wu, Wen-Tian Chen, Wei-Kang Dou, Hui-Min Zhou, Ming S |
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- Page last updated:Jun 11, 2024
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