HuGE Literature Finder
Records 1-17
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Genetic mutation analysis of the COQ2 gene in Italian patients with multiple system atrophy.
Gene 2019 Aug 144037. Procopio Radha, Gagliardi Monica, Brighina Laura, Nicoletti Giuseppe, Morelli Maurizio, Ferrarese Carlo, Annesi Grazia, Quattrone Al |
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Lack of association of mortalin (HSPA9) and other mitochondria-related genes with risk of Parkinson's and Alzheimer's diseases.
Neurobiology of aging 2017 Jan 49 215.e9-215.e10. Chung Sun Ju, Kim Mi-Jung, Ryu Ho-Sung, Kim Juyeon, Kim Young Jin, Kim Kiju, You Sooyeoun, Kim Seong Yoon, Lee Jae-Ho |
A genome-wide association study in multiple system atrophy.
Neurology 2016 Sep . Sailer Anna, Scholz Sonja W, Nalls Michael A, Schulte Claudia, Federoff Monica, Price T Ryan, Lees Andrew, Ross Owen A, Dickson Dennis W, Mok Kin, Mencacci Niccolo E, Schottlaender Lucia, Chelban Viorica, Ling Helen, O'Sullivan Sean S, Wood Nicholas W, Traynor Bryan J, Ferrucci Luigi, Federoff Howard J, Mhyre Timothy R, Morris Huw R, Deuschl Günther, Quinn Niall, Widner Hakan, Albanese Alberto, Infante Jon, Bhatia Kailash P, Poewe Werner, Oertel Wolfgang, Höglinger Günter U, Wüllner Ullrich, Goldwurm Stefano, Pellecchia Maria Teresa, Ferreira Joaquim, Tolosa Eduardo, Bloem Bastiaan R, Rascol Olivier, Meissner Wassilios G, Hardy John A, Revesz Tamas, Holton Janice L, Gasser Thomas, Wenning Gregor K, Singleton Andrew B, Houlden Henry, |
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Mutational analysis of COQ2 in patients with MSA in Italy.
Neurobiology of aging 2016 Jun . Ronchi Dario, Di Biase Ernesto, Franco Giulia, Melzi Valentina, Del Sorbo Francesca, Elia Antonio, Barzaghi Chiara, Garavaglia Barbara, Bergamini Christian, Fato Romana, Mora Gabriele, Del Bo Roberto, Fortunato Francesco, Borellini Linda, Trezzi Ilaria, Compagnoni Giacomo Monzio, Monfrini Edoardo, Frattini Emanuele, Bonato Sara, Cogiamanian Filippo, Ardolino Gianluca, Priori Alberto, Bresolin Nereo, Corti Stefania, Comi Giacomo Pietro, Di Fonzo Aless |
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MAPT haplotype diversity in multiple system atrophy.
Parkinsonism & related disorders 2016 09 30 40-5. Labbé Catherine, Heckman Michael G, Lorenzo-Betancor Oswaldo, Murray Melissa E, Ogaki Kotaro, Soto-Ortolaza Alexandra I, Walton Ronald L, Fujioka Shinsuke, Koga Shunsuke, Uitti Ryan J, van Gerpen Jay A, Petersen Ronald C, Graff-Radford Neill R, Younkin Steven G, Boeve Bradley F, Cheshire William P, Low Phillip A, Sandroni Paola, Coon Elizabeth A, Singer Wolfgang, Wszolek Zbigniew K, Dickson Dennis W, Ross Owen |
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Serum Levels of Coenzyme Q10 in Patients with Multiple System Atrophy.
PloS one 2016 11 (1): e0147574. Kasai Takashi, Tokuda Takahiko, Ohmichi Takuma, Ishii Ryotaro, Tatebe Harutsugu, Nakagawa Masanori, Mizuno Toshi |
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Association of the COQ2 V393A variant with risk of multiple system atrophy in East Asians: a case-control study and meta-analysis of the literature.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2015 Nov . Zhao QuanZhen, Yang Xinglong, Tian SiJia, An Ran, Zheng JinHua, Xu Yanmi |
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Mutation Analysis of COQ2 in Chinese Patients with Cerebellar Subtype of Multiple System Atrophy.
CNS neuroscience & therapeutics 2015 Aug 21 (8): 626-30. Wen Xiao-Dan, Li Hong-Fu, Wang Hong-Xia, Ni Wang, Dong Yi, Wu Zhi-Yi |
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Lack of evidence for an association between the V393A variant of COQ2 and amyotrophic lateral sclerosis in a Han Chinese population.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2015 Jul 36 (7): 1211-5. Yang Xinglong, Xi Jing, An Ran, Yu Lihua, Lin Zhenfang, Zhou Huayong, Xu Yanmi |
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Brain energy metabolism in early MSA-P: A phosphorus and proton magnetic resonance spectroscopy study.
Parkinsonism & related disorders 2015 May 21 (5): 533-5. Stamelou M, Pilatus U, Reuss A, Respondek G, Knake S, Oertel W H, Höglinger G |
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COQ2 gene variants associate with cerebellar subtype of multiple system atrophy in Chinese.
Movement disorders : official journal of the Movement Disorder Society 2015 Mar 30 (3): 436-7. Lin Chin-Hsien, Tan Eng-King, Yang Chih-Chao, Yi Zhao, Wu Ruey-Me |
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Mutation scanning of the COQ2 gene in ethnic Chinese patients with multiple-system atrophy.
Neurobiology of aging 2015 Feb 36 (2): 1222.e7-11. Chen Yong Ping, Zhao Bi, Cao Bei, Song Wei, Guo XiaoYan, Wei Qian-Qian, Yang Yuan, Yuan Li Xing, Shang Hui-Fa |
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COQ2 p.V393A variant, rs148156462, is not associated with Parkinson's disease in a Taiwanese population.
Neurobiology of aging 2015 Jan 36 (1): 546.e17-8. Lin Chin-Hsien, Lin Hang-I, Chen Meng-Ling, Wu Ruey-Me |
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Association of the COQ2 V393A Variant with Parkinson's Disease: A Case-Control Study and Meta-Analysis.
PloS one 2015 10 (6): e0130970. Yang Xinglong, Xi Jing, Zhao Quanzhen, Jia Hua, An Ran, Liu Zhuolin, Xu Yanmi |
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[Susceptibility gene in multiple system atrophy (MSA)].
Rinsh? shinkeigaku = Clinical neurology 2014 54 (12): 969-71. Tsuji Sho |
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Analysis of COQ2 gene in multiple system atrophy.
Molecular neurodegeneration 2014 9 44. Ogaki Kotaro, Fujioka Shinsuke, Heckman Michael G, Rayaprolu Sruti, Soto-Ortolaza Alexandra I, Labbé Catherine, Walton Ronald L, Lorenzo-Betancor Oswaldo, Wang Xue, Asmann Yan, Rademakers Rosa, Graff-Radford Neill, Uitti Ryan, Cheshire William P, Wszolek Zbigniew K, Dickson Dennis W, Ross Owen |
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Mutations in COQ2 in familial and sporadic multiple-system atrophy.
The New England journal of medicine 2013 Jul 369 (3): 233-44. Authors are not available |
- Page last reviewed:Mar 16, 2019
- Page last updated:Apr 01, 2020
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