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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 17, 2025. (Total: 235411Documents)
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Records 1 - 9 (of 9 Records)

Query Trace: Movement Disorders and FMR1[original query]
Fragile X premutation alleles in SCA, ET, and parkinsonism in an Asian cohort.
Neurology 2004 Jul 63 (2): 362-3.
Tan E K, Zhao Y, Puong K Y, Law H Y, Chan L L, Yew K, Tan C, Shen H, Chandran V R, Teoh M L, Yih Y, Pavanni R, Wong M C, Ng I
FMR1 premutations associated with fragile X-associated tremor/ataxia syndrome in multiple system atrophy.
Archives of neurology 2005 Jun 62 (6): 962-6.
Biancalana Valérie, Toft Mathias, Le Ber Isabelle, Tison François, Scherrer Elisabeth, Thibodeau Stephen, Mandel Jean Louis, Brice Alexis, Farrer Matthew J, Dürr Alexand
Screening for FXTAS in 95 Spanish patients negative for Huntington disease.
Genetic testing 2008 Mar 12 (1): 135-8.
Rodriguez-Revenga Laia, Santos M Mònica, Sánchez Aurora, Pujol Montserrat, Gómez-Anson Beatriz, Badenas Celia, Jiménez Dolores, Madrigal Irene, Milà Montserr
Small CGG repeat expansion alleles of FMR1 gene are associated with parkinsonism.
Clinical genetics 2009 Nov 76 (5): 471-6.
Loesch D Z, Khaniani M S, Slater H R, Rubio J P, Bui Q M, Kotschet K, D'Souza W, Venn A, Kalitsis P, Choo A K H, Burgess T, Johnson L, Evans A, Horne
FXTAS is rare among Portuguese patients with movement disorders: FMR1 premutations may be associated with a wider spectrum of phenotypes.
Behavioral and brain functions : BBF 2011 7 (1): 19.
Seixas Ana I, Vale José, Jorge Paula, Marques Isabel, Santos Rosário, Alonso Isabel, Fortuna Ana M, Pinto-Basto Jorge, Coutinho Paula, Margolis Russell L, Sequeiros Jorge, Silveira Isab
Clinical implication of FMR1 intermediate alleles in a Spanish population.
Clinical genetics 2018 Mar .
Alvarez-Mora M I, Madrigal I, Martinez F, Tejada M-I, Izquierdo-Alvarez S, Sanchez-Villar de Saz P, Caro-Llopis A, Villate O, Rodríguez-Santiago B, Pérez Jurado L A, Rodriguez-Revenga L, Milà
Characterization of the Cerebrospinal Fluid Proteome in Patients with Fragile X-Associated Tremor/Ataxia Syndrome.
Cerebellum (London, England) 2021 5 21 (1): 86-98.
Abbasi Diana A, Nguyen Thu T A, Hall Deborah A, Robertson-Dick Erin, Berry-Kravis Elizabeth, Cologna Stephanie
GIPC1 CGG Repeat Expansion Is Associated with Movement Disorders.
Annals of neurology 2022 2 91 (5): 704-715.
Fan Yu, Shen Si, Yang Jing, Yao Dabao, Li Mengjie, Mao Chengyuan, Wang Yunchao, Hao Xiaoyan, Ma Dongrui, Li Jiadi, Shi Jingjing, Guo Mengnan, Li Shuangjie, Yuan Yanpeng, Liu Fen, Yang Zhihua, Zhang Shuo, Hu Zhengwei, Fan Liyuan, Liu Han, Zhang Chan, Wang Yanlin, Wang Qingzhi, Zheng Hong, He Ying, Song Bo, Xu Yuming, Shi Chang
Evaluation of the role of FMR1 CGG repeat allele in Parkinson's disease from the Chinese population.
Frontiers in aging neuroscience 2023 8 15 1234027.
Juan Chen, Yuwen Zhao, Xun Zhou, Jin Xue, Qiao Xiao, Hongxu Pan, Xiaoxia Zhou, Yaqin Xiang, Jian Li, Liping Zhu, Zhou Zhou, Yang Yang, Qian Xu, Qiying Sun, Xinxiang Yan, Jieqiong Tan, Jinchen Li, Jifeng Guo, Ranhui Duan, Beisha Tang, Qiao Yu, Zhenhua L
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